Skip to main content
Erschienen in: Drugs 13/2001

01.11.2001 | Therapy in Practice

Cervical Dystonia

Pathophysiology and Treatment Options

verfasst von: Dr Miodrag Velickovic, Reina Benabou, Mitchell F. Brin

Erschienen in: Drugs | Ausgabe 13/2001

Einloggen, um Zugang zu erhalten

Abstract

Dystonia is a syndrome of sustained involuntary muscle contractions, frequently causing twisting and repetitive movements or abnormal posturing. Cervical dystonia (CD) is a form of dystonia that involves neck muscles. However, CD is not the only cause of neck rotation. Torticollis may be caused by orthopaedic, musculofibrotic, infectious and other neurological conditions that affect the anatomy of the neck, and structural causes.
It is estimated that there are between 60 000 and 90 000 patients with CD in the US. The majority of the patients present with a combination of neck rotation (rotatory torticollis or rotatocollis), flexion (anterocollis), extension (retrocollis), head tilt (laterocollis) or a lateral or sagittal shift. Neck posturing may be either tonic, clonic or tremulous, and may result in permanent and fixed contractures.
Sensory tricks (‘geste antagonistique’) often temporarily ameliorate dystonic movements and postures. Commonly used sensory tricks by patients with CD include touching the chin, back of the head or top of the head.
Patients with CD are classified according to aetiology into two groups: primary CD (idiopathic — may be genetic or sporadic) or secondary CD (symptomatic). Patients with primary CD have no evidence by history, physical examination or laboratory studies (except primary dystonia gene) of any secondary cause for the dystonic symptoms. CD is a part of either generalised or focal dystonic syndrome which may have a genetic basis, with an identifiable genetic association. Secondary or symptomatic CD may be caused by central or peripheral trauma, exposure to dopamine receptor antagonists (tardive), neurodegenerative disease, and other conditions associated with abnormal functioning of the basal ganglia. In the majority of patients with CD, the aetiology is not identifiable and the disorder is often classified as primary.
Unless the aetiological investigation reveals a specific therapeutic intervention, therapy for CD is symptomatic. It includes supportive therapy and counselling, physical therapy, pharmacotherapy, chemodenervation [botulinum toxin (BTX), phenol, alcohol], and central and peripheral surgical therapy. The most widely used and accepted therapy for CD is local intramuscular injections of BTX-type A. Currently, both BTX type A and type B are commercially available, and type F has undergone testing. Pharmacotherapy, including anticholinergics, dopaminergic depleting and blocking agents, and other muscle relaxants can be used alone or in combination with other therapeutic interventions. Surgery is usually reserved for patients with CD in whom other forms of treatment have failed.
Fußnoten
1
Use of a tradename is for identification purposes only and does not imply endorsement.
 
2
Use of a tradename is for identification purposes only and does not imply endorsement.
 
3
Use of a tradename is for identification purposes only and does not imply endorsement.
 
4
Use of a tradename is for identification purposes only and does not imply endorsement.
 
Literatur
1.
Zurück zum Zitat Fahn S, Marsden CD, Calne DB. Classification and investigation of dystonia. In: Marsden CD, Fahn S, editors. Movement disorders 2. London: Butterworths, 1987: 332–58 Fahn S, Marsden CD, Calne DB. Classification and investigation of dystonia. In: Marsden CD, Fahn S, editors. Movement disorders 2. London: Butterworths, 1987: 332–58
2.
Zurück zum Zitat Fahn S. The varied clinical expressions of dystonia. Neurol Clin 1984; 2(3): 541–54PubMed Fahn S. The varied clinical expressions of dystonia. Neurol Clin 1984; 2(3): 541–54PubMed
3.
Zurück zum Zitat Claypool DW, Duane DD, Ilstrup DM, et al. Epidemiology and outcome of cervical dystonia (spasmodic torticollis) in Rochester, Minnesota. Mov Disord 1995; 10: 608–14PubMedCrossRef Claypool DW, Duane DD, Ilstrup DM, et al. Epidemiology and outcome of cervical dystonia (spasmodic torticollis) in Rochester, Minnesota. Mov Disord 1995; 10: 608–14PubMedCrossRef
4.
Zurück zum Zitat Nutt JG, Muenter MD, Aronson A, et al. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord 1988; 3: 188–94PubMedCrossRef Nutt JG, Muenter MD, Aronson A, et al. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord 1988; 3: 188–94PubMedCrossRef
5.
Zurück zum Zitat Duffey PO, Butler AG, Hawthorne MR, et al. The epidemiology of the primary dystonias in the north of England. Adv Neurol 1998; 78: 121–5PubMed Duffey PO, Butler AG, Hawthorne MR, et al. The epidemiology of the primary dystonias in the north of England. Adv Neurol 1998; 78: 121–5PubMed
6.
Zurück zum Zitat Chan J, Brin M, Fahn S. Idiopathic cervical dystonia: clinical characteristics. Mov Disord 1991; 6: 119–26PubMedCrossRef Chan J, Brin M, Fahn S. Idiopathic cervical dystonia: clinical characteristics. Mov Disord 1991; 6: 119–26PubMedCrossRef
7.
Zurück zum Zitat Jankovic J, Leder S, Warner D, et al. Cervical dystonia: clinical findings and associated movement disorders. Neurology 1991; 41: 1088–91PubMedCrossRef Jankovic J, Leder S, Warner D, et al. Cervical dystonia: clinical findings and associated movement disorders. Neurology 1991; 41: 1088–91PubMedCrossRef
8.
Zurück zum Zitat Rondot P, Marchand MP, Dellatolas G. Spasmodic torticollis — review of 220 patients. Can J Neurol Sci 1991; 18: 143–51PubMed Rondot P, Marchand MP, Dellatolas G. Spasmodic torticollis — review of 220 patients. Can J Neurol Sci 1991; 18: 143–51PubMed
9.
Zurück zum Zitat Duane DD. Spasmodic torticollis. Adv Neurol 1988;49: 135–50PubMed Duane DD. Spasmodic torticollis. Adv Neurol 1988;49: 135–50PubMed
10.
Zurück zum Zitat Epidemiologic Study of Dystonia in Europe (ESDE) Collaborative Group. Sex-related influences on the frequency and age of onset of primary dystonia. Neurology 1999; 53: 1871–3CrossRef Epidemiologic Study of Dystonia in Europe (ESDE) Collaborative Group. Sex-related influences on the frequency and age of onset of primary dystonia. Neurology 1999; 53: 1871–3CrossRef
11.
Zurück zum Zitat Marsden CD. Investigation of dystonia. Adv Neurol 1988; 50: 35–44PubMed Marsden CD. Investigation of dystonia. Adv Neurol 1988; 50: 35–44PubMed
12.
Zurück zum Zitat Consky ES, Lang AE. Clinical assessments of patients with cervical Dystonia. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994: 211–37 Consky ES, Lang AE. Clinical assessments of patients with cervical Dystonia. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994: 211–37
13.
Zurück zum Zitat Jorgenson C, Porphyris H. Idiopathic spasmodic torticollis. J Neurosurg Nurs 1985; 17: 169–74PubMedCrossRef Jorgenson C, Porphyris H. Idiopathic spasmodic torticollis. J Neurosurg Nurs 1985; 17: 169–74PubMedCrossRef
14.
Zurück zum Zitat Friedman A, Fahn S. Spontaneous remissions in spasmodic torticollis. Neurology 1986; 36: 398–400PubMedCrossRef Friedman A, Fahn S. Spontaneous remissions in spasmodic torticollis. Neurology 1986; 36: 398–400PubMedCrossRef
15.
Zurück zum Zitat Jahanshahi M, Marion MH, Marsden CD. Natural history of adult-onset idiopathic torticollis. Arch Neurol 1990; 47: 548–52PubMedCrossRef Jahanshahi M, Marion MH, Marsden CD. Natural history of adult-onset idiopathic torticollis. Arch Neurol 1990; 47: 548–52PubMedCrossRef
16.
Zurück zum Zitat Jahanshahi M. Factors that ameliorate or aggravate spasmodic torticollis. J Neurol Neurosurg Psychiatry 2000; 68: 227–9PubMedCrossRef Jahanshahi M. Factors that ameliorate or aggravate spasmodic torticollis. J Neurol Neurosurg Psychiatry 2000; 68: 227–9PubMedCrossRef
17.
Zurück zum Zitat Wissel J, Müller J, Ebersbach G, et al. Trick maneuvers in cervical dystonia: investigation of movement- and touch-related changes in polymyographic activity. Mov Disord 1999; 14: 994–9PubMedCrossRef Wissel J, Müller J, Ebersbach G, et al. Trick maneuvers in cervical dystonia: investigation of movement- and touch-related changes in polymyographic activity. Mov Disord 1999; 14: 994–9PubMedCrossRef
18.
Zurück zum Zitat Greene PE, Bressman S. Exteroceptive and interoceptive stimuli in dystonia. Mov Disord 1998; 13: 549–5PubMedCrossRef Greene PE, Bressman S. Exteroceptive and interoceptive stimuli in dystonia. Mov Disord 1998; 13: 549–5PubMedCrossRef
19.
Zurück zum Zitat Kutvonen O, Dastidar P, Nurmikko T. Pain in spasmodic torticollis. Pain 1997; 69(3): 279–86PubMedCrossRef Kutvonen O, Dastidar P, Nurmikko T. Pain in spasmodic torticollis. Pain 1997; 69(3): 279–86PubMedCrossRef
20.
Zurück zum Zitat Lowenstein DH, Aminoff MJ. The clinical course of spasmodic torticollis. Neurology 1988; 38: 530–2PubMedCrossRef Lowenstein DH, Aminoff MJ. The clinical course of spasmodic torticollis. Neurology 1988; 38: 530–2PubMedCrossRef
21.
Zurück zum Zitat Bressman SB, Sabatti C, Raymond D, et al. The dystonial phe-notype and guidelines for diagnostic testing [see comments]. Neurology 2000; 54: 1746–52PubMedCrossRef Bressman SB, Sabatti C, Raymond D, et al. The dystonial phe-notype and guidelines for diagnostic testing [see comments]. Neurology 2000; 54: 1746–52PubMedCrossRef
22.
Zurück zum Zitat Brin MF. Dystonia: genetics and treatment with botulinum toxin. In: Smith B, Adelman G, editors. Neuroscience year: encyclopedia of neuroscience. Suppl. 2. Boston: Birkhauser, 1997: 56–8 Brin MF. Dystonia: genetics and treatment with botulinum toxin. In: Smith B, Adelman G, editors. Neuroscience year: encyclopedia of neuroscience. Suppl. 2. Boston: Birkhauser, 1997: 56–8
23.
Zurück zum Zitat Ozelius LJ, Hewett JW, Page CE, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP binding protein. Natl Gen 1997; 17: 40–8CrossRef Ozelius LJ, Hewett JW, Page CE, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP binding protein. Natl Gen 1997; 17: 40–8CrossRef
24.
Zurück zum Zitat Ozelius L, Kramer PL, Moskowitz CB, et al. Human gene for torsion dystonia located on chromosome 9q32-q 34. Neuron 1989; 2: 1427–34PubMedCrossRef Ozelius L, Kramer PL, Moskowitz CB, et al. Human gene for torsion dystonia located on chromosome 9q32-q 34. Neuron 1989; 2: 1427–34PubMedCrossRef
25.
Zurück zum Zitat Gimenez-Roldan S, Lopez-Fraile IP, Esteban A. Dystonia in Spain: study of a Gypsy family and general survey. Adv Neurol 1976; 14: 125–36PubMed Gimenez-Roldan S, Lopez-Fraile IP, Esteban A. Dystonia in Spain: study of a Gypsy family and general survey. Adv Neurol 1976; 14: 125–36PubMed
26.
Zurück zum Zitat Haberhausen G, Schmitt I, Köhler A, et al. Assignment of the dystonia-parkinsonism syndrome locus, dystonia3, to a small region within a 1.8-Mb YAC contig of Xql3. 1. Am J Hum Genet 1995; 57: 644–50 Haberhausen G, Schmitt I, Köhler A, et al. Assignment of the dystonia-parkinsonism syndrome locus, dystonia3, to a small region within a 1.8-Mb YAC contig of Xql3. 1. Am J Hum Genet 1995; 57: 644–50
27.
Zurück zum Zitat Graeber MB, Kupke KG, Muller U. Delineation of the dystonia-parkinsonism syndrome locus in Xq l 3. Proc Natl Acad Sci U S A 1992; 89: 8245–8PubMedCrossRef Graeber MB, Kupke KG, Muller U. Delineation of the dystonia-parkinsonism syndrome locus in Xq l 3. Proc Natl Acad Sci U S A 1992; 89: 8245–8PubMedCrossRef
28.
Zurück zum Zitat Takahashi H, Snow B, Waters C, et al. Evidence for nigrostriatal lesions in Lubag (X-linked dystonia-parkinsonism in the Philippines). Neurology 1992; 42 Suppl. 3: 441CrossRef Takahashi H, Snow B, Waters C, et al. Evidence for nigrostriatal lesions in Lubag (X-linked dystonia-parkinsonism in the Philippines). Neurology 1992; 42 Suppl. 3: 441CrossRef
29.
Zurück zum Zitat Lee LV, Kupke KG, Caballar Gonzaga F, et al. The phenotype of the X-linked dystonia-parkinsonism syndrome. An assessment of 42 cases in the Philippines. Medicine (Balt) 1991; 70: 179–87 Lee LV, Kupke KG, Caballar Gonzaga F, et al. The phenotype of the X-linked dystonia-parkinsonism syndrome. An assessment of 42 cases in the Philippines. Medicine (Balt) 1991; 70: 179–87
30.
Zurück zum Zitat Wilhelmsen KC, Weeks DE, Nygaard TG, et al. Genetic mapping of the ‘Lubag’ (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Ann Neurol 1991; 29: 124–31PubMedCrossRef Wilhelmsen KC, Weeks DE, Nygaard TG, et al. Genetic mapping of the ‘Lubag’ (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Ann Neurol 1991; 29: 124–31PubMedCrossRef
31.
Zurück zum Zitat Kupke KG, Lee LV, Muller U. Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis. Neurology 1990; 40: 1438–42PubMedCrossRef Kupke KG, Lee LV, Muller U. Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis. Neurology 1990; 40: 1438–42PubMedCrossRef
32.
Zurück zum Zitat Kupke KG, Lee LV, Viterbo GH, et al. X-linked recessive torsion dystonia in the Philippines. Am J Med Genet 1990; 36: 237–42PubMedCrossRef Kupke KG, Lee LV, Viterbo GH, et al. X-linked recessive torsion dystonia in the Philippines. Am J Med Genet 1990; 36: 237–42PubMedCrossRef
33.
Zurück zum Zitat Kandil MR, Tohamy SA, Fattah MA, et al. Prevalence of chorea, dystonia and athetosis in Assiut, Egypt: a clinical and epidemiological study. Neuroepidemiology 1994; 13: 202–10PubMedCrossRef Kandil MR, Tohamy SA, Fattah MA, et al. Prevalence of chorea, dystonia and athetosis in Assiut, Egypt: a clinical and epidemiological study. Neuroepidemiology 1994; 13: 202–10PubMedCrossRef
34.
35.
Zurück zum Zitat Ichinose H, Ohye T, Takahashi E, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet 1994; 8: 236–42PubMedCrossRef Ichinose H, Ohye T, Takahashi E, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet 1994; 8: 236–42PubMedCrossRef
36.
Zurück zum Zitat Ichinose H, Ohye T, Matsuda Y, et al. Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency. J Biol Chem 1995; 270: 10062–71 Ichinose H, Ohye T, Matsuda Y, et al. Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency. J Biol Chem 1995; 270: 10062–71
37.
Zurück zum Zitat Nygaard TG, Wilhelmsen KC, Risch NJ, et al. Linkage mapping of DOPA-responsive dystonia (Drd) to chromosome 14Q. Nat Genet 1993; 5: 386–91PubMedCrossRef Nygaard TG, Wilhelmsen KC, Risch NJ, et al. Linkage mapping of DOPA-responsive dystonia (Drd) to chromosome 14Q. Nat Genet 1993; 5: 386–91PubMedCrossRef
38.
Zurück zum Zitat Knappskog PM, Flatmark T, Mallet J, et al. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene. Hum Mol Genet 1995; 4: 1209–12PubMedCrossRef Knappskog PM, Flatmark T, Mallet J, et al. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene. Hum Mol Genet 1995; 4: 1209–12PubMedCrossRef
39.
Zurück zum Zitat Almasy L, Bressman SB, Raymond D, et al. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families. Ann Neurol 1997; 42: 670–3PubMedCrossRef Almasy L, Bressman SB, Raymond D, et al. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families. Ann Neurol 1997; 42: 670–3PubMedCrossRef
40.
Zurück zum Zitat Leube B, Rudnicki D, Ratzlaff T, et al. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a german family with adult onset, autosomal dominant inheritance and purely focal distribution. Hum Mol Genet 1996; 5: 1673–7PubMedCrossRef Leube B, Rudnicki D, Ratzlaff T, et al. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a german family with adult onset, autosomal dominant inheritance and purely focal distribution. Hum Mol Genet 1996; 5: 1673–7PubMedCrossRef
41.
Zurück zum Zitat Leube B, Hendgen T, Kessler KR, et al. Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p. Ann Neurol 1997; 42(1): 111–4PubMedCrossRef Leube B, Hendgen T, Kessler KR, et al. Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p. Ann Neurol 1997; 42(1): 111–4PubMedCrossRef
42.
Zurück zum Zitat Leube B, Hendgen T, Kessler KR, et al. Evidence for dystonia7 being a common cause of cervical dystonia (torticollis) in Central Europe. Am J Med Genet 1997; 74(5): 529–2PubMedCrossRef Leube B, Hendgen T, Kessler KR, et al. Evidence for dystonia7 being a common cause of cervical dystonia (torticollis) in Central Europe. Am J Med Genet 1997; 74(5): 529–2PubMedCrossRef
43.
Zurück zum Zitat Raskind WH, Bolin T, Wolff J, et al. Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q 34. Hum Genet 1998; 102: 93–7PubMedCrossRef Raskind WH, Bolin T, Wolff J, et al. Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q 34. Hum Genet 1998; 102: 93–7PubMedCrossRef
44.
Zurück zum Zitat Fink JK, Rainer S, Wilkowski J, et al. Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. Am J Hum Genet 1996; 59: 140–5PubMed Fink JK, Rainer S, Wilkowski J, et al. Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. Am J Hum Genet 1996; 59: 140–5PubMed
45.
Zurück zum Zitat Fouad GT, Servidei S, Durcan S, et al. A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet 1996; 59: 135–9PubMed Fouad GT, Servidei S, Durcan S, et al. A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet 1996; 59: 135–9PubMed
46.
Zurück zum Zitat Auburger G, Ratzlaff T, Lunkes A, et al. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S 197. Genomics 1996; 31: 90–4PubMedCrossRef Auburger G, Ratzlaff T, Lunkes A, et al. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S 197. Genomics 1996; 31: 90–4PubMedCrossRef
47.
Zurück zum Zitat Walker ES. Familial paroxysmal dystonic choreoathetosis: a neurologic disorder simulating psychiatric illness. Johns Hopkins Med J 1981; 148: 108–13PubMed Walker ES. Familial paroxysmal dystonic choreoathetosis: a neurologic disorder simulating psychiatric illness. Johns Hopkins Med J 1981; 148: 108–13PubMed
48.
Zurück zum Zitat Kertesz A. Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied. Neurology 1967; 17: 680–90 Kertesz A. Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied. Neurology 1967; 17: 680–90
49.
Zurück zum Zitat Lance JW. Sporadic and familial varieties of tonic seizures. J Neurol Neurosurg Psychiatry 1963; 26: 51–9PubMedCrossRef Lance JW. Sporadic and familial varieties of tonic seizures. J Neurol Neurosurg Psychiatry 1963; 26: 51–9PubMedCrossRef
50.
Zurück zum Zitat Smith LA, Heersema PH. Periodic dystonia. Mayo Clin Proc 1941; 16: 842–6 Smith LA, Heersema PH. Periodic dystonia. Mayo Clin Proc 1941; 16: 842–6
51.
Zurück zum Zitat Klein C, Brin MF, Kramer P, et al. Association of a missense change in the D2 dopamine receptor with myoclonus dystonia. Proc Natl Acad Sci U S A 1999; 96: 5173–6PubMedCrossRef Klein C, Brin MF, Kramer P, et al. Association of a missense change in the D2 dopamine receptor with myoclonus dystonia. Proc Natl Acad Sci U S A 1999; 96: 5173–6PubMedCrossRef
52.
Zurück zum Zitat Klein C, Breakefield X, Ozelius L. Genetics of primary dystonia. Semin Neurol 1999; 19: 271–80PubMedCrossRef Klein C, Breakefield X, Ozelius L. Genetics of primary dystonia. Semin Neurol 1999; 19: 271–80PubMedCrossRef
53.
Zurück zum Zitat Gasser T, Bereznai B, Muller B, et al. Linkage studies in alcohol-responsive myoclonic dystonia. Mov Disord 1996; 11: 363–70PubMedCrossRef Gasser T, Bereznai B, Muller B, et al. Linkage studies in alcohol-responsive myoclonic dystonia. Mov Disord 1996; 11: 363–70PubMedCrossRef
54.
Zurück zum Zitat Nygaard TG, Raymond D, Chen C, et al. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q 31. Ann Neurol 1999; 46: 794–8PubMedCrossRef Nygaard TG, Raymond D, Chen C, et al. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q 31. Ann Neurol 1999; 46: 794–8PubMedCrossRef
55.
Zurück zum Zitat Brashear A, deLeon D, Bressman SB, et al. Rapid-onset dystonia-parkinsonism in a second family. Neurology 1997; 48(4): 1066–9PubMedCrossRef Brashear A, deLeon D, Bressman SB, et al. Rapid-onset dystonia-parkinsonism in a second family. Neurology 1997; 48(4): 1066–9PubMedCrossRef
56.
Zurück zum Zitat Ishikawa A, Miyatake T. A family with hereditary juvenile dystonia-parkinsonism. Mov Disord 1995; 10: 482–8PubMedCrossRef Ishikawa A, Miyatake T. A family with hereditary juvenile dystonia-parkinsonism. Mov Disord 1995; 10: 482–8PubMedCrossRef
57.
Zurück zum Zitat Dobyns WB, Ozelius LJ, Kramer PL, et al. Rapid-onset dystonia-parkinsonism. Neurology 1993; 43: 2596–602PubMedCrossRef Dobyns WB, Ozelius LJ, Kramer PL, et al. Rapid-onset dystonia-parkinsonism. Neurology 1993; 43: 2596–602PubMedCrossRef
58.
Zurück zum Zitat Kramer PL, Mineta M, Klein C, et al. Rapid-onset dystonia-parkinsonism: linkage to chromosome 19ql3 [in process citation]. Ann Neurol 1999; 46: 176–82PubMedCrossRef Kramer PL, Mineta M, Klein C, et al. Rapid-onset dystonia-parkinsonism: linkage to chromosome 19ql3 [in process citation]. Ann Neurol 1999; 46: 176–82PubMedCrossRef
59.
Zurück zum Zitat Jun AS, Brown MD, Wallace DC. A mitochondrial DNA mutation at np 14459 of the ND6 gene associated with maternally inherited Leber’s hereditary optic neuropathy and dystonia. Proc Natl Acad Sci U S A 1994; 91: 6206–10PubMedCrossRef Jun AS, Brown MD, Wallace DC. A mitochondrial DNA mutation at np 14459 of the ND6 gene associated with maternally inherited Leber’s hereditary optic neuropathy and dystonia. Proc Natl Acad Sci U S A 1994; 91: 6206–10PubMedCrossRef
60.
Zurück zum Zitat Novotny Jr EJ, Singh G, Wallace DC, et al. Leber’s disease and dystonia: a mitochondrial disease. Neurology 1986; 36: 1053–60PubMedCrossRef Novotny Jr EJ, Singh G, Wallace DC, et al. Leber’s disease and dystonia: a mitochondrial disease. Neurology 1986; 36: 1053–60PubMedCrossRef
61.
Zurück zum Zitat Risch N, de Leon D, Ozelius L, et al. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population [see comments]. Natl Genet 1995; 9: 152–9CrossRef Risch N, de Leon D, Ozelius L, et al. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population [see comments]. Natl Genet 1995; 9: 152–9CrossRef
62.
Zurück zum Zitat Kramer PL, de Leon D, Ozelius L, et al. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34 [see comments]. Ann Neurol 1990; 27: 114–20PubMedCrossRef Kramer PL, de Leon D, Ozelius L, et al. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34 [see comments]. Ann Neurol 1990; 27: 114–20PubMedCrossRef
63.
Zurück zum Zitat Shashidharan P, Kramer BC, Walker RH, et al. Immunohisto-chemical localization and distribution of torsinA in normal human and rat brain. Brain Res 2000; 853: 197–206PubMedCrossRef Shashidharan P, Kramer BC, Walker RH, et al. Immunohisto-chemical localization and distribution of torsinA in normal human and rat brain. Brain Res 2000; 853: 197–206PubMedCrossRef
64.
Zurück zum Zitat Shashidharan P, Good PF, Hsu A, et al. Torsin A accumulation in Lewy bodies in sporadic Parkinson’s disease. Brain Res 2000; 877(2): 379–81PubMedCrossRef Shashidharan P, Good PF, Hsu A, et al. Torsin A accumulation in Lewy bodies in sporadic Parkinson’s disease. Brain Res 2000; 877(2): 379–81PubMedCrossRef
65.
Zurück zum Zitat Augood SJ, Martin DM, Ozelius LJ, et al. Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain. Ann Neurol 1999; 46: 761–9PubMedCrossRef Augood SJ, Martin DM, Ozelius LJ, et al. Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain. Ann Neurol 1999; 46: 761–9PubMedCrossRef
66.
Zurück zum Zitat Kustedjo K, Bracey MH, Cravatt BF. Torsin A and its torsion dystonia-associated mutant form are lumenal glycoproteins that exhibit distinct subcellular localizations. J Biol Chem 2000; 275(36): 27933–9PubMed Kustedjo K, Bracey MH, Cravatt BF. Torsin A and its torsion dystonia-associated mutant form are lumenal glycoproteins that exhibit distinct subcellular localizations. J Biol Chem 2000; 275(36): 27933–9PubMed
67.
Zurück zum Zitat Hewett J, Gonzalez-Agosti C, Slater D, et al. Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells. Hum Mol Genet 2000; 9: 1403–13PubMedCrossRef Hewett J, Gonzalez-Agosti C, Slater D, et al. Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells. Hum Mol Genet 2000; 9: 1403–13PubMedCrossRef
68.
Zurück zum Zitat Oppenheim H. Uber eine eigenartige Krampfkrankheit des kindlichen und jungendichen Alters (dysbasia lordotica progressiva, dystonia musculorum deformans). Neuro Centrabl 1911; 30: 1090–107 Oppenheim H. Uber eine eigenartige Krampfkrankheit des kindlichen und jungendichen Alters (dysbasia lordotica progressiva, dystonia musculorum deformans). Neuro Centrabl 1911; 30: 1090–107
69.
Zurück zum Zitat Herz EM, Dystonia I. Historical review; analysis of dystonic symptoms and physiologic mechanisms involved. Arch Neurol Psychiatry 1944; 51: 305–55CrossRef Herz EM, Dystonia I. Historical review; analysis of dystonic symptoms and physiologic mechanisms involved. Arch Neurol Psychiatry 1944; 51: 305–55CrossRef
70.
Zurück zum Zitat Herz E. Dystonia III. Pathology and conclusions. Arch Neurol Psychiatry 1944; 52: 20–6CrossRef Herz E. Dystonia III. Pathology and conclusions. Arch Neurol Psychiatry 1944; 52: 20–6CrossRef
71.
Zurück zum Zitat Herz E. Dystonia II. Clinical classification. Arch Neurol Psychiatry 1944; 51: 319–55 Herz E. Dystonia II. Clinical classification. Arch Neurol Psychiatry 1944; 51: 319–55
72.
Zurück zum Zitat Cohen LG, Hallett M. Hand cramps: clinical features and electromyographic patterns in a focal dystonia. Neurology 1988; 38: 1005–12PubMedCrossRef Cohen LG, Hallett M. Hand cramps: clinical features and electromyographic patterns in a focal dystonia. Neurology 1988; 38: 1005–12PubMedCrossRef
73.
Zurück zum Zitat Buchman AS, Cornelia CL, Leurgans S, et al. The effect of changes in head posture on the patterns of muscle activity in cervical dystonia (CD). Mov Disord 1998; 13: 490–6PubMedCrossRef Buchman AS, Cornelia CL, Leurgans S, et al. The effect of changes in head posture on the patterns of muscle activity in cervical dystonia (CD). Mov Disord 1998; 13: 490–6PubMedCrossRef
74.
Zurück zum Zitat Hallett M. Physiology of dystonia. Adv Neurol 1998; 78: 11–8PubMed Hallett M. Physiology of dystonia. Adv Neurol 1998; 78: 11–8PubMed
75.
Zurück zum Zitat Kaji R, Rothwell JC, Katayama M, et al. Tonic vibration reflex and muscle afferent block in writer’s cramp. Ann Neurol 1995; 38: 155–62PubMedCrossRef Kaji R, Rothwell JC, Katayama M, et al. Tonic vibration reflex and muscle afferent block in writer’s cramp. Ann Neurol 1995; 38: 155–62PubMedCrossRef
76.
Zurück zum Zitat Naumann M, Pirker W, Reiners K, et al. Imaging the pre- and postsynaptic side of striatal dopaminergic synapses in idiopathic cervical dystonia: a SPECT study using [123I] epidepride and [123I] beta-CIT. Mov Disord 1998; 13: 319–23PubMedCrossRef Naumann M, Pirker W, Reiners K, et al. Imaging the pre- and postsynaptic side of striatal dopaminergic synapses in idiopathic cervical dystonia: a SPECT study using [123I] epidepride and [123I] beta-CIT. Mov Disord 1998; 13: 319–23PubMedCrossRef
77.
Zurück zum Zitat Perlmutter JS, Stambuk MK, Markham J, et al. Decreased [18F]spiperone binding in putamen in dystonia. Adv Neurol 1998; 78: 161–8PubMed Perlmutter JS, Stambuk MK, Markham J, et al. Decreased [18F]spiperone binding in putamen in dystonia. Adv Neurol 1998; 78: 161–8PubMed
78.
Zurück zum Zitat Sealfon SC, Olanow CW. Dopamine receptors: from structure to behavior. Trends Neurosci 2000; 23: S34–S40PubMedCrossRef Sealfon SC, Olanow CW. Dopamine receptors: from structure to behavior. Trends Neurosci 2000; 23: S34–S40PubMedCrossRef
79.
Zurück zum Zitat Kanovsky P, Streitova H, Dufek J, et al. Lateralization of the P22/N30 component of somatosensory evoked potentials of the median nerve in patients with cervical dystonia. Mov Disord 1997; 12(4): 553–60PubMedCrossRef Kanovsky P, Streitova H, Dufek J, et al. Lateralization of the P22/N30 component of somatosensory evoked potentials of the median nerve in patients with cervical dystonia. Mov Disord 1997; 12(4): 553–60PubMedCrossRef
80.
Zurück zum Zitat McEwen JE, Reilly PR. State legislative efforts to regulate use and potential misuse of genetic information [published erratum appears in Am J Hum Genet 1992 Dec; 51 (6): 1457]. Am J Hum Genet 1992; 51: 637–47PubMed McEwen JE, Reilly PR. State legislative efforts to regulate use and potential misuse of genetic information [published erratum appears in Am J Hum Genet 1992 Dec; 51 (6): 1457]. Am J Hum Genet 1992; 51: 637–47PubMed
81.
Zurück zum Zitat Mazzini L, Zaccala M, Balzarini C. Abnormalities of somatosensory evoked potentials in spasmodic torticollis. Mov Disord 1994; 9: 426–30PubMedCrossRef Mazzini L, Zaccala M, Balzarini C. Abnormalities of somatosensory evoked potentials in spasmodic torticollis. Mov Disord 1994; 9: 426–30PubMedCrossRef
82.
Zurück zum Zitat Naumann M, MagyarLehmann S, Reiners K, et al. Sensory tricks in cervical dystonia: perceptual dysbalance of parietal cortex modulates frontal motor programming. Ann Neurol 2000; 47(3): 322–8PubMedCrossRef Naumann M, MagyarLehmann S, Reiners K, et al. Sensory tricks in cervical dystonia: perceptual dysbalance of parietal cortex modulates frontal motor programming. Ann Neurol 2000; 47(3): 322–8PubMedCrossRef
83.
Zurück zum Zitat Leis AA, Dimitrijevic MR, Delapasse JS, et al. Modification of cervical dystonia by selective sensory stimulation. J Neurol Sci 1992; 110: 79–89PubMedCrossRef Leis AA, Dimitrijevic MR, Delapasse JS, et al. Modification of cervical dystonia by selective sensory stimulation. J Neurol Sci 1992; 110: 79–89PubMedCrossRef
84.
Zurück zum Zitat Odergren T, Rimpilainen I, Borg J. Sternocleidomastoid muscle responses to transcranial magnetic stimulation in patients with cervical dystonia. Electromyogr Motor Control 1997; 105(1): 44–52 Odergren T, Rimpilainen I, Borg J. Sternocleidomastoid muscle responses to transcranial magnetic stimulation in patients with cervical dystonia. Electromyogr Motor Control 1997; 105(1): 44–52
85.
Zurück zum Zitat Amadio S, Panizza M, Pisano F, et al. Transcranial magnetic stimulation and silent period in spasmodic torticollis. Am J Phys Med Rehabil 2000; 79: 361–8PubMedCrossRef Amadio S, Panizza M, Pisano F, et al. Transcranial magnetic stimulation and silent period in spasmodic torticollis. Am J Phys Med Rehabil 2000; 79: 361–8PubMedCrossRef
86.
Zurück zum Zitat Samii A, Pal PK, Schulzer M, et al. Post-traumatic cervical dystonia: a distinct entity? Can J Neurol Sci 2000; 27(1): 55–9PubMed Samii A, Pal PK, Schulzer M, et al. Post-traumatic cervical dystonia: a distinct entity? Can J Neurol Sci 2000; 27(1): 55–9PubMed
87.
Zurück zum Zitat Truong DD, Dubinsky R, Hermanowicz N, et al. Posttraumatic torticollis. Arch Neurol 1991; 48: 221–3PubMedCrossRef Truong DD, Dubinsky R, Hermanowicz N, et al. Posttraumatic torticollis. Arch Neurol 1991; 48: 221–3PubMedCrossRef
88.
Zurück zum Zitat Tarsy D. Comparison of acute- and delayed-onset posttraumatic cervical dystonia. Mov Disord 1998: 13; 481–5PubMedCrossRef Tarsy D. Comparison of acute- and delayed-onset posttraumatic cervical dystonia. Mov Disord 1998: 13; 481–5PubMedCrossRef
89.
Zurück zum Zitat Schott GD. The relationship of peripheral trauma and pain to dystonia. J Neurol Neurosurg Psychiatry 1985; 48: 698–701PubMedCrossRef Schott GD. The relationship of peripheral trauma and pain to dystonia. J Neurol Neurosurg Psychiatry 1985; 48: 698–701PubMedCrossRef
90.
Zurück zum Zitat Duane DD, Clark M, Gottlob L. Elevated autoimmune antibody titers in cervical dystonia versus control. Neurology 1995; 45: A456CrossRef Duane DD, Clark M, Gottlob L. Elevated autoimmune antibody titers in cervical dystonia versus control. Neurology 1995; 45: A456CrossRef
91.
Zurück zum Zitat Kumar R, Maraganore DM, Ahlskog JE, et al. Treatment of putative immune-mediated and idiopathic cervical dystonia with intravenous methylprednisolone. Neurology 1997; 48: 732–5PubMedCrossRef Kumar R, Maraganore DM, Ahlskog JE, et al. Treatment of putative immune-mediated and idiopathic cervical dystonia with intravenous methylprednisolone. Neurology 1997; 48: 732–5PubMedCrossRef
92.
Zurück zum Zitat Becker G, Berg D, Rausch WD, et al. Increased tissue copper and manganese content in the lentiform nucleus in primary adult-onset dystonia. Ann Neurol 1999; 46(2): 260–3PubMedCrossRef Becker G, Berg D, Rausch WD, et al. Increased tissue copper and manganese content in the lentiform nucleus in primary adult-onset dystonia. Ann Neurol 1999; 46(2): 260–3PubMedCrossRef
93.
Zurück zum Zitat Berg D, Weishaupt A, Francis MJ, et al. Changes of copper-transporting proteins and ceruloplasmin in the lentiform nuclei in primary adult-onset dystonia. Ann Neurol 2000; 47(6): 827–30PubMedCrossRef Berg D, Weishaupt A, Francis MJ, et al. Changes of copper-transporting proteins and ceruloplasmin in the lentiform nuclei in primary adult-onset dystonia. Ann Neurol 2000; 47(6): 827–30PubMedCrossRef
94.
Zurück zum Zitat Mezaki T, Matsumoto S, Hamada C, et al. Decreased serum ceruloplasmin and copper levels in cervical dystonia. Ann Neurol 2001; 49(1): 138–9PubMedCrossRef Mezaki T, Matsumoto S, Hamada C, et al. Decreased serum ceruloplasmin and copper levels in cervical dystonia. Ann Neurol 2001; 49(1): 138–9PubMedCrossRef
95.
Zurück zum Zitat Weiner WJ, Lang AE. Idiopathic torsion dystonia. In: Weiner WJ, Lang AE, editors. Movement disorders: a comprehensive survey. New York: Futura, 1989: 347–418 Weiner WJ, Lang AE. Idiopathic torsion dystonia. In: Weiner WJ, Lang AE, editors. Movement disorders: a comprehensive survey. New York: Futura, 1989: 347–418
96.
Zurück zum Zitat Jankovic J, Fahn S. Dystonic syndromes. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore-Munich: Urban & Schwarzenberg, 1988: 283–314 Jankovic J, Fahn S. Dystonic syndromes. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore-Munich: Urban & Schwarzenberg, 1988: 283–314
97.
Zurück zum Zitat Dauer WT, Burke RE, Greene P, et al. Current concepts on the clinical features, etiology and management of idiopathic cervical dystonia. Brain 1998; 121: 547–60PubMedCrossRef Dauer WT, Burke RE, Greene P, et al. Current concepts on the clinical features, etiology and management of idiopathic cervical dystonia. Brain 1998; 121: 547–60PubMedCrossRef
98.
Zurück zum Zitat Scott BL. Evaluation and treatment of dystonia. South Med J 2000; 93: 746–51PubMed Scott BL. Evaluation and treatment of dystonia. South Med J 2000; 93: 746–51PubMed
99.
Zurück zum Zitat Pal PK, Samii A, Schulzer M, et al. Head tremor in cervical dystonia. Can J Neurol Sci 2000; 27: 137–42PubMed Pal PK, Samii A, Schulzer M, et al. Head tremor in cervical dystonia. Can J Neurol Sci 2000; 27: 137–42PubMed
100.
Zurück zum Zitat de Leon D, Moskowitz CB, Stewart C. Proposed guidelines for videotaping individuals with movement disorders. J Neurosci Nurs 1991; 23: 191–3PubMedCrossRef de Leon D, Moskowitz CB, Stewart C. Proposed guidelines for videotaping individuals with movement disorders. J Neurosci Nurs 1991; 23: 191–3PubMedCrossRef
101.
Zurück zum Zitat Klawans HL. Taking a Risk. Trials of an expert witness: tales of clinical neurology and the law. Boston: Little Brown, 1991: 93–4 Klawans HL. Taking a Risk. Trials of an expert witness: tales of clinical neurology and the law. Boston: Little Brown, 1991: 93–4
102.
Zurück zum Zitat Kraft IA. A psychiatric study of two patients with dystonia musculorum deformans. South Med J 1966; 59: 284–8PubMedCrossRef Kraft IA. A psychiatric study of two patients with dystonia musculorum deformans. South Med J 1966; 59: 284–8PubMedCrossRef
103.
Zurück zum Zitat Tolosa ES. Clinical features of Meige’s disease (idiopathic or-ofacial dystonia). iA report of 17 cases. Arch Neurol 1981; 38: 147–51PubMedCrossRef Tolosa ES. Clinical features of Meige’s disease (idiopathic or-ofacial dystonia). iA report of 17 cases. Arch Neurol 1981; 38: 147–51PubMedCrossRef
104.
Zurück zum Zitat Jahanshahi M, Marsden CD. Depression in torticollis: a controlled study. Psychol Med 1988; 18: 925–33PubMedCrossRef Jahanshahi M, Marsden CD. Depression in torticollis: a controlled study. Psychol Med 1988; 18: 925–33PubMedCrossRef
105.
Zurück zum Zitat Jahanshahi M, Marsden CD. A longitudinal follow-up study of depression, disability, and body concept in torticollis. Behav Neurol 1990; 3: 233–46 Jahanshahi M, Marsden CD. A longitudinal follow-up study of depression, disability, and body concept in torticollis. Behav Neurol 1990; 3: 233–46
106.
Zurück zum Zitat Murry T, Cannito MP, Woodson GE. Spasmodic Dysphonia -emotional status and Botulinum toxin treatment. Arch Otolaryngol Head Neck Surg 1994; 120: 310–6PubMedCrossRef Murry T, Cannito MP, Woodson GE. Spasmodic Dysphonia -emotional status and Botulinum toxin treatment. Arch Otolaryngol Head Neck Surg 1994; 120: 310–6PubMedCrossRef
107.
Zurück zum Zitat Lauterbach EC, Price ST, Spears TE, et al. Serotonin responsive and nonresponsive diurnal depressive mood disorders and pathological affect in Thalamic Infarct associated with Myoclonus and Blepharospasm. Biol Psychiatry 1994; 35: 488–90PubMedCrossRef Lauterbach EC, Price ST, Spears TE, et al. Serotonin responsive and nonresponsive diurnal depressive mood disorders and pathological affect in Thalamic Infarct associated with Myoclonus and Blepharospasm. Biol Psychiatry 1994; 35: 488–90PubMedCrossRef
108.
Zurück zum Zitat Jahanshahi M. Psychosocial factors and depression in torticollis. J Psychosom Res 1991; 35: 493–507PubMedCrossRef Jahanshahi M. Psychosocial factors and depression in torticollis. J Psychosom Res 1991; 35: 493–507PubMedCrossRef
109.
Zurück zum Zitat Wenzel T, Schnider P, Wimmer A, et al. Psychiatric comorbidity in patients with spasmodic torticollis. J Psychosom Res 1998; 44: 687–90PubMedCrossRef Wenzel T, Schnider P, Wimmer A, et al. Psychiatric comorbidity in patients with spasmodic torticollis. J Psychosom Res 1998; 44: 687–90PubMedCrossRef
110.
Zurück zum Zitat Greene P, Shale H, Fahn S. Analysis of open-label trials in torsion dystonia using high dosages of anticholinergics and other drugs. Mov Disord 1988; 3: 46–60PubMedCrossRef Greene P, Shale H, Fahn S. Analysis of open-label trials in torsion dystonia using high dosages of anticholinergics and other drugs. Mov Disord 1988; 3: 46–60PubMedCrossRef
111.
Zurück zum Zitat Brans JW, Lindeboom R, Snoek JW, et al. Botulinum toxin versus trihexyphenidyl in cervical dystonia: a prospective, randomized, double-blind controlled trial. Neurology 1996; 46: 1066–72PubMedCrossRef Brans JW, Lindeboom R, Snoek JW, et al. Botulinum toxin versus trihexyphenidyl in cervical dystonia: a prospective, randomized, double-blind controlled trial. Neurology 1996; 46: 1066–72PubMedCrossRef
112.
Zurück zum Zitat Reches A, Burke RE, Kuhn CM, et al. Tetrabenazine, an amine-depleting drug, also blocks dopamine receptors in rat brain. J Pharmacol Exp Ther 1983; 225: 515–21PubMed Reches A, Burke RE, Kuhn CM, et al. Tetrabenazine, an amine-depleting drug, also blocks dopamine receptors in rat brain. J Pharmacol Exp Ther 1983; 225: 515–21PubMed
113.
Zurück zum Zitat Jankovic J. Treatment of hyperkinetic movement disorders with tetrabenazine: a double-blind crossover study. Ann Neurol 1982; 11: 41–7PubMedCrossRef Jankovic J. Treatment of hyperkinetic movement disorders with tetrabenazine: a double-blind crossover study. Ann Neurol 1982; 11: 41–7PubMedCrossRef
114.
Zurück zum Zitat Jankovic J, Orman J. Tetrabenazine therapy of dystonia, chorea, tics, and other dyskinesias. Neurology 1988; 38: 391–4PubMedCrossRef Jankovic J, Orman J. Tetrabenazine therapy of dystonia, chorea, tics, and other dyskinesias. Neurology 1988; 38: 391–4PubMedCrossRef
115.
Zurück zum Zitat Jankovic J, Beach J. Long-term effects of tetrabenazine in hyperkinetic movement disorders. Neurology 1997; 48: 358–62PubMedCrossRef Jankovic J, Beach J. Long-term effects of tetrabenazine in hyperkinetic movement disorders. Neurology 1997; 48: 358–62PubMedCrossRef
116.
Zurück zum Zitat Burke RE, Reches A, Traub MM, et al. Tetrabenazine induces acute dystonic reactions. Ann Neurol 1985; 17: 200–2PubMedCrossRef Burke RE, Reches A, Traub MM, et al. Tetrabenazine induces acute dystonic reactions. Ann Neurol 1985; 17: 200–2PubMedCrossRef
117.
Zurück zum Zitat Burke RE, Fahn S, Mayeux R, et al. Neuroleptic malignant syndrome caused by dopamine-depleting drugs in a patient with Huntington disease. Neurology 1981; 31: 1022–5PubMedCrossRef Burke RE, Fahn S, Mayeux R, et al. Neuroleptic malignant syndrome caused by dopamine-depleting drugs in a patient with Huntington disease. Neurology 1981; 31: 1022–5PubMedCrossRef
118.
Zurück zum Zitat Ossemann M, Sindic CJ, Laterre C. Tetrabenazine as a cause of neuroleptic malignant syndrome [letter]. Mov Disord 1996; 11: 95PubMedCrossRef Ossemann M, Sindic CJ, Laterre C. Tetrabenazine as a cause of neuroleptic malignant syndrome [letter]. Mov Disord 1996; 11: 95PubMedCrossRef
119.
Zurück zum Zitat Mateo D, Munoz-Blanco JL, Gimenez-Roldan S. Neuroleptic malignant syndrome related to tetrabenazine introduction and haloperidol discontinuation in Huntington’s disease. Clin Neuropharm 1992; 15: 63–8CrossRef Mateo D, Munoz-Blanco JL, Gimenez-Roldan S. Neuroleptic malignant syndrome related to tetrabenazine introduction and haloperidol discontinuation in Huntington’s disease. Clin Neuropharm 1992; 15: 63–8CrossRef
120.
Zurück zum Zitat Burbaud P, Guehl D, Lagueny A, et al. A pilot trial of clozapine in the treatment of cervical dystonia [letter]. J Neurol 1998; 245: 329–31PubMedCrossRef Burbaud P, Guehl D, Lagueny A, et al. A pilot trial of clozapine in the treatment of cervical dystonia [letter]. J Neurol 1998; 245: 329–31PubMedCrossRef
121.
Zurück zum Zitat Thiel A, Dressier D, Kistel C, et al. Clozapine treatment of spasmodic torticollis. Neurology 1994; 44: 957–8PubMedCrossRef Thiel A, Dressier D, Kistel C, et al. Clozapine treatment of spasmodic torticollis. Neurology 1994; 44: 957–8PubMedCrossRef
122.
Zurück zum Zitat Karpati S, Desaknai S, Desaknai M, et al. Human herpesvirus type 8-positive facial angiosarcoma developing at the site of botulinum toxin injection for blepharospasm. Br J Dermatol 2000; 143: 660–1PubMedCrossRef Karpati S, Desaknai S, Desaknai M, et al. Human herpesvirus type 8-positive facial angiosarcoma developing at the site of botulinum toxin injection for blepharospasm. Br J Dermatol 2000; 143: 660–1PubMedCrossRef
123.
Zurück zum Zitat Scott AB, Rosenbaum A, Collins CC. Pharmacologic weakening of extraocular muscles. Invest Ophthalmol Vis Sci 1973; 12: 924–7 Scott AB, Rosenbaum A, Collins CC. Pharmacologic weakening of extraocular muscles. Invest Ophthalmol Vis Sci 1973; 12: 924–7
124.
Zurück zum Zitat Scott AB. Botulinum toxin injection into extraocular muscles as an alternative to strabismus surgery. J Pediatr Ophthalmol Strabismus 1980; 17: 21–5PubMed Scott AB. Botulinum toxin injection into extraocular muscles as an alternative to strabismus surgery. J Pediatr Ophthalmol Strabismus 1980; 17: 21–5PubMed
125.
Zurück zum Zitat Brin MF, Fahn S, Moskowitz C, et al. Localized injections of botulinum toxin for the treatment of focal dystonia and hemi-facial spasm. Adv Neurol 1988; 50: 599–608PubMed Brin MF, Fahn S, Moskowitz C, et al. Localized injections of botulinum toxin for the treatment of focal dystonia and hemi-facial spasm. Adv Neurol 1988; 50: 599–608PubMed
126.
Zurück zum Zitat Jankovic J, Schwartz K. Botulinum toxin injections for cervical dystonia. Neurology 1990; 40: 277–80PubMedCrossRef Jankovic J, Schwartz K. Botulinum toxin injections for cervical dystonia. Neurology 1990; 40: 277–80PubMedCrossRef
127.
Zurück zum Zitat Cornelia CL, Buchman AS, Tanner CM, et al. Botulinum toxin injection for spasmodic torticollis: increased magnitude of benefit with electromyographic assistance. Neurology 1992; 42: 878–82CrossRef Cornelia CL, Buchman AS, Tanner CM, et al. Botulinum toxin injection for spasmodic torticollis: increased magnitude of benefit with electromyographic assistance. Neurology 1992; 42: 878–82CrossRef
128.
Zurück zum Zitat Greene P, Kang U, Fahn S, et al. Double-blind, placebo-controlled trial of botulinum toxin injections for the treatment of spasmodic torticollis. Neurology 1990; 40: 1213–8PubMedCrossRef Greene P, Kang U, Fahn S, et al. Double-blind, placebo-controlled trial of botulinum toxin injections for the treatment of spasmodic torticollis. Neurology 1990; 40: 1213–8PubMedCrossRef
129.
130.
Zurück zum Zitat Brin MF. Interventional neurology: treatment of neurological conditions with local injection of botulinum toxin. Arch Neurobiol 1991; 54: 173–89 Brin MF. Interventional neurology: treatment of neurological conditions with local injection of botulinum toxin. Arch Neurobiol 1991; 54: 173–89
131.
Zurück zum Zitat Jahanshahi M, Marsden CD. Psychological functioning before and after treatment of torticollis with botulinum toxin. J Neurol Neurosurg Psychiatry 1992; 55: 229–31PubMedCrossRef Jahanshahi M, Marsden CD. Psychological functioning before and after treatment of torticollis with botulinum toxin. J Neurol Neurosurg Psychiatry 1992; 55: 229–31PubMedCrossRef
132.
Zurück zum Zitat Poewe W, Deuschl G, Nebe A, et al. What is the optimal dose of botulinum toxin A in the treatment of cervical dystonia? Results of a double blind, placebo controlled, dose ranging study using Dysport®. J Neurol Neurosurg Psychiatry 1998; 64(1): 13–7PubMedCrossRef Poewe W, Deuschl G, Nebe A, et al. What is the optimal dose of botulinum toxin A in the treatment of cervical dystonia? Results of a double blind, placebo controlled, dose ranging study using Dysport®. J Neurol Neurosurg Psychiatry 1998; 64(1): 13–7PubMedCrossRef
133.
Zurück zum Zitat Brans JW, Lindeboom R, Aramideh M, et al. Long-term effect of botulinum toxin on impairment and functional health in cervical dystonia. Neurology 1998; 50: 1461–3PubMedCrossRef Brans JW, Lindeboom R, Aramideh M, et al. Long-term effect of botulinum toxin on impairment and functional health in cervical dystonia. Neurology 1998; 50: 1461–3PubMedCrossRef
134.
Zurück zum Zitat Kessler KR, Skutta M, Benecke R. Long-term treatment of cervical dystonia with botulinum toxin A: efficacy, safety, and antibody frequency. German Dystonia Study Group J Neurol 1999; 246: 265–74 Kessler KR, Skutta M, Benecke R. Long-term treatment of cervical dystonia with botulinum toxin A: efficacy, safety, and antibody frequency. German Dystonia Study Group J Neurol 1999; 246: 265–74
135.
Zurück zum Zitat Odergren T, Hjaltason H, Kaakkola S, et al. A double blind, randomised, parallel group study to investigate the dose equivalence of Dysport(R) and Botox(R) in the treatment of cervical dystonia. J Neurol Neurosurg Psychiatry 1998; 64(1):6–12PubMedCrossRef Odergren T, Hjaltason H, Kaakkola S, et al. A double blind, randomised, parallel group study to investigate the dose equivalence of Dysport(R) and Botox(R) in the treatment of cervical dystonia. J Neurol Neurosurg Psychiatry 1998; 64(1):6–12PubMedCrossRef
136.
Zurück zum Zitat Dressler D, Rothwell JC. Electromyographic quantification of the paralysing effect of botulinum toxin in the sternocleido-mastoid muscle. Eur Neurol 2000; 43: 13–6PubMedCrossRef Dressler D, Rothwell JC. Electromyographic quantification of the paralysing effect of botulinum toxin in the sternocleido-mastoid muscle. Eur Neurol 2000; 43: 13–6PubMedCrossRef
137.
Zurück zum Zitat Brashear A, Bergan K, Wojcieszek J, et al. Patients’ perception of stopping or continuing treatment of cervical dystonia with botulinum toxin type A. Mov Disord 2000; 15(1): 150–3PubMedCrossRef Brashear A, Bergan K, Wojcieszek J, et al. Patients’ perception of stopping or continuing treatment of cervical dystonia with botulinum toxin type A. Mov Disord 2000; 15(1): 150–3PubMedCrossRef
138.
Zurück zum Zitat Astarloa R, Morales B, Sanchez V, et al. [Focal dystonias and facial hemispasm: treatment with botulinum A toxin]. Arch Neurobiol 1991; 54 Suppl. 3: 44–51 Astarloa R, Morales B, Sanchez V, et al. [Focal dystonias and facial hemispasm: treatment with botulinum A toxin]. Arch Neurobiol 1991; 54 Suppl. 3: 44–51
139.
Zurück zum Zitat Finsterer J, Fuchs I, Mamoli B. Automatic EMG-guided botulinum toxin treatment of spasticity. Clin Neuropharmacol 1997; 20(3): 195–203PubMedCrossRef Finsterer J, Fuchs I, Mamoli B. Automatic EMG-guided botulinum toxin treatment of spasticity. Clin Neuropharmacol 1997; 20(3): 195–203PubMedCrossRef
140.
Zurück zum Zitat Finsterer J, Fuchs I, Mamoli B. Quantitative electromyography-guided botulinum toxin treatment of cervical dystonia. Clin Neuropharmacol 1997; 20: 42–8PubMedCrossRef Finsterer J, Fuchs I, Mamoli B. Quantitative electromyography-guided botulinum toxin treatment of cervical dystonia. Clin Neuropharmacol 1997; 20: 42–8PubMedCrossRef
141.
Zurück zum Zitat Brans JW, de Boer IP, Aramideh M, et al. Botulinum toxin in cervical dystonia: low dosage with electromyographic guidance. J Neurol 1995; 242: 529–34PubMedCrossRef Brans JW, de Boer IP, Aramideh M, et al. Botulinum toxin in cervical dystonia: low dosage with electromyographic guidance. J Neurol 1995; 242: 529–34PubMedCrossRef
142.
Zurück zum Zitat Rollnik JD, Matzke M, Wohlfarth K, et al. Low-dose treatment of cervical dystonia, blepharospasm and facial hemispasm with albumin-diluted botulinum toxin type A under EMG guidance — an open label study. Eur Neurol 2000; 43(1): 9–12PubMedCrossRef Rollnik JD, Matzke M, Wohlfarth K, et al. Low-dose treatment of cervical dystonia, blepharospasm and facial hemispasm with albumin-diluted botulinum toxin type A under EMG guidance — an open label study. Eur Neurol 2000; 43(1): 9–12PubMedCrossRef
143.
Zurück zum Zitat Brin MF, Blitzer A. Botulinum toxin — dangerous terminology errors. J R Soc Med 1993; 86: 494 Brin MF, Blitzer A. Botulinum toxin — dangerous terminology errors. J R Soc Med 1993; 86: 494
144.
Zurück zum Zitat Sampaio C, Ferreira JJ, Simoes F, et al. DYSBOT: a single-blind, randomized parallel study to determine whether any differences can be detected in the efficacy and tolerability of two formulations of botulinum toxin type A — Dysport and Botox — assuming a ratio of 4: 1. Mov Disord 1997; 12(6): 1013–8PubMedCrossRef Sampaio C, Ferreira JJ, Simoes F, et al. DYSBOT: a single-blind, randomized parallel study to determine whether any differences can be detected in the efficacy and tolerability of two formulations of botulinum toxin type A — Dysport and Botox — assuming a ratio of 4: 1. Mov Disord 1997; 12(6): 1013–8PubMedCrossRef
145.
Zurück zum Zitat Brashear A, Lew M F, Dykstra DD, et al. Safety & efficacy of Neurobloc (botulinum toxin type B) in type A-responsive cervical dystonia. Neurology 1999; 53(7): 1439–46PubMedCrossRef Brashear A, Lew M F, Dykstra DD, et al. Safety & efficacy of Neurobloc (botulinum toxin type B) in type A-responsive cervical dystonia. Neurology 1999; 53(7): 1439–46PubMedCrossRef
146.
Zurück zum Zitat Brin MF, Lew MF, Adler CH, et al. Safety & efficacy of Neurobloc (botulinum toxin type B) in type-A resistant cervical dystonia. Neurology 1999; 53(7): 1431–8PubMedCrossRef Brin MF, Lew MF, Adler CH, et al. Safety & efficacy of Neurobloc (botulinum toxin type B) in type-A resistant cervical dystonia. Neurology 1999; 53(7): 1431–8PubMedCrossRef
147.
Zurück zum Zitat Jankovic J, Brin MF. Botulinum toxin: historical perspective and potential new indications. Muscle Nerve 1997; 20: S129–45CrossRef Jankovic J, Brin MF. Botulinum toxin: historical perspective and potential new indications. Muscle Nerve 1997; 20: S129–45CrossRef
148.
Zurück zum Zitat Brin MF. Treatment of dystonia. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. New York: Williams & Wilkins, 1998: 553–78 Brin MF. Treatment of dystonia. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. New York: Williams & Wilkins, 1998: 553–78
149.
Zurück zum Zitat Brin MF, Blitzer A, Stewart C, et al. Disorders with excessive muscle contraction: candidates for treatment with intramuscular botulinum toxin (‘botox’). In: DasGupta BR, editor. Botulinum and tetanus neurotoxins: neurotransmission and biomedical aspects. New York: Plenum, 1993: 559–76 Brin MF, Blitzer A, Stewart C, et al. Disorders with excessive muscle contraction: candidates for treatment with intramuscular botulinum toxin (‘botox’). In: DasGupta BR, editor. Botulinum and tetanus neurotoxins: neurotransmission and biomedical aspects. New York: Plenum, 1993: 559–76
150.
Zurück zum Zitat Blitzer A, Binder WJ, Brin MF. Management of facial wrinkles with botulinum toxin injections. In: Krespi YP, editor. Office-based surgery of the head and neck. New York: Lippincott-Raven, 1998: 251–4 Blitzer A, Binder WJ, Brin MF. Management of facial wrinkles with botulinum toxin injections. In: Krespi YP, editor. Office-based surgery of the head and neck. New York: Lippincott-Raven, 1998: 251–4
151.
Zurück zum Zitat Blitzer A, Binder WJ, Boyd JB, et al. Management of facial lines and wrinkles. Philadelphia: Lippincott Williams & Wilkins, 1999 Blitzer A, Binder WJ, Boyd JB, et al. Management of facial lines and wrinkles. Philadelphia: Lippincott Williams & Wilkins, 1999
152.
Zurück zum Zitat American Academy of Neurology. Assessment: the clinical usefulness of botulinum toxin-A in treating neurologic disorders. Report of the therapeutics and technology assessment subcommittee of the American Academy of Neurology. Neurology 1990; 40: 1332–6 American Academy of Neurology. Assessment: the clinical usefulness of botulinum toxin-A in treating neurologic disorders. Report of the therapeutics and technology assessment subcommittee of the American Academy of Neurology. Neurology 1990; 40: 1332–6
153.
Zurück zum Zitat National Institutes of Health Consensus Development Conference. Clinical use of botulinum toxin. National Institutes of Health Consensus Development Statement, Nov 12–14, 1990. Arch Neurol 1991; 48: 1294–8 National Institutes of Health Consensus Development Conference. Clinical use of botulinum toxin. National Institutes of Health Consensus Development Statement, Nov 12–14, 1990. Arch Neurol 1991; 48: 1294–8
154.
Zurück zum Zitat AAO-HNS. American Academy of Otolaryngology — Head and neck surgery policy statement: Botox for spasmodic dysphonia. AAO-HNS Bulletin 1990; 9: 8 AAO-HNS. American Academy of Otolaryngology — Head and neck surgery policy statement: Botox for spasmodic dysphonia. AAO-HNS Bulletin 1990; 9: 8
155.
Zurück zum Zitat Cornelia CL, Tanner CM, DeFoor-Hill L, et al. Dysphagia after botulinum toxin injections for spasmodic torticollis: clinical and radiologic findings. Neurology 1992; 42: 1307–10CrossRef Cornelia CL, Tanner CM, DeFoor-Hill L, et al. Dysphagia after botulinum toxin injections for spasmodic torticollis: clinical and radiologic findings. Neurology 1992; 42: 1307–10CrossRef
156.
Zurück zum Zitat Buchholz DW, Neumann S. The swallowing side effects of botulinum toxin type a injection in spasmodic dysphonia. Dysphagia 1997; 12: 59–60PubMedCrossRef Buchholz DW, Neumann S. The swallowing side effects of botulinum toxin type a injection in spasmodic dysphonia. Dysphagia 1997; 12: 59–60PubMedCrossRef
157.
Zurück zum Zitat Lew MF, Adornato BT, Duane DD, et al. Botulinum toxin type B (BotB): a double-blind, placebo-controlled, safety and efficacy study in cervical dystonia. Neurology 1997; 49: 701–7PubMedCrossRef Lew MF, Adornato BT, Duane DD, et al. Botulinum toxin type B (BotB): a double-blind, placebo-controlled, safety and efficacy study in cervical dystonia. Neurology 1997; 49: 701–7PubMedCrossRef
159.
Zurück zum Zitat Allergan Inc. BOTOX® package information. Irvine (CA), 2000 Allergan Inc. BOTOX® package information. Irvine (CA), 2000
160.
Zurück zum Zitat Paton JC, Lawrence AJ, Manson JI. Quantitation of Clostridium botulinum organisms and toxin in the feces of an infant with botulism. J Clin Microbiol 1982; 15: 1–4PubMed Paton JC, Lawrence AJ, Manson JI. Quantitation of Clostridium botulinum organisms and toxin in the feces of an infant with botulism. J Clin Microbiol 1982; 15: 1–4PubMed
161.
Zurück zum Zitat Jankovic J, Schwartz K. Response and immunoresistance to botulinum toxin injections. Neurology 1995; 45: 1743–6PubMedCrossRef Jankovic J, Schwartz K. Response and immunoresistance to botulinum toxin injections. Neurology 1995; 45: 1743–6PubMedCrossRef
162.
Zurück zum Zitat Sankhla C, Jankovic J, Duane D. Variability of the immunologic and clinical response in dystonic patients immunoresist-ant to botulinum toxin injections. Movement Disord 1998; 13(1): 150–4PubMedCrossRef Sankhla C, Jankovic J, Duane D. Variability of the immunologic and clinical response in dystonic patients immunoresist-ant to botulinum toxin injections. Movement Disord 1998; 13(1): 150–4PubMedCrossRef
163.
Zurück zum Zitat Greene P, Fahn S. Development of antibodies to botulinum toxin type A in patients with torticollis treated with injections of botulinum toxin type A. In: DasGupta BR, editor. Botulinum and tetanus neurotoxins: neurotransmission and biomedical aspects. New York: Plenum Press, 1993: 651–4 Greene P, Fahn S. Development of antibodies to botulinum toxin type A in patients with torticollis treated with injections of botulinum toxin type A. In: DasGupta BR, editor. Botulinum and tetanus neurotoxins: neurotransmission and biomedical aspects. New York: Plenum Press, 1993: 651–4
164.
Zurück zum Zitat Greene P, Fahn S, Diamond B. Development of resistance to botulinum toxin type A in patients with torticollis. Mov Disord 1994; 9: 213–7PubMedCrossRef Greene P, Fahn S, Diamond B. Development of resistance to botulinum toxin type A in patients with torticollis. Mov Disord 1994; 9: 213–7PubMedCrossRef
165.
Zurück zum Zitat Zuber M, Sebald M, Bathien N, et al. Botulinum antibodies in Dystonic patients treated with Type-A Botulinum Toxin —frequency and significance. Neurology 1993; 43: 1715–8PubMedCrossRef Zuber M, Sebald M, Bathien N, et al. Botulinum antibodies in Dystonic patients treated with Type-A Botulinum Toxin —frequency and significance. Neurology 1993; 43: 1715–8PubMedCrossRef
166.
Zurück zum Zitat Hatheway CH, Snyder JD, Seals JE, et al. Antitoxin levels in botulism patients treated with trivalent equine botulism antitoxin to toxin types A, B, and E. J Infect Dis 1984; 150: 407–12PubMedCrossRef Hatheway CH, Snyder JD, Seals JE, et al. Antitoxin levels in botulism patients treated with trivalent equine botulism antitoxin to toxin types A, B, and E. J Infect Dis 1984; 150: 407–12PubMedCrossRef
167.
Zurück zum Zitat Dressier D, Dimberger G, Bhatia KP, et al. Botulinum toxin antibody testing: comparison between the mouse protection assay and the mouse lethality assay. Mov Disord 2000; 15: 973–6CrossRef Dressier D, Dimberger G, Bhatia KP, et al. Botulinum toxin antibody testing: comparison between the mouse protection assay and the mouse lethality assay. Mov Disord 2000; 15: 973–6CrossRef
168.
Zurück zum Zitat Dezfulian M, Hatheway C, Yolken R, et al. Enzyme-linked immunosorbent assay for detection of Clostridium botulinum type A and type B toxins in stool samples of infants with botulism. J Clin Microbiol 1984; 20: 379–83PubMed Dezfulian M, Hatheway C, Yolken R, et al. Enzyme-linked immunosorbent assay for detection of Clostridium botulinum type A and type B toxins in stool samples of infants with botulism. J Clin Microbiol 1984; 20: 379–83PubMed
169.
Zurück zum Zitat Dezfulian M, Bitar R, Bartlett J. Kinetics study of immunological response to Clostridium botulinum toxin. J Clin Microbiol 1987; 25: 1336–7PubMed Dezfulian M, Bitar R, Bartlett J. Kinetics study of immunological response to Clostridium botulinum toxin. J Clin Microbiol 1987; 25: 1336–7PubMed
170.
Zurück zum Zitat Tsui JK, Wong NLM, Wong E, et al. Production of circulating antibodies to botulinum-A toxin in patients receiving repeated injections for dystonia. Ann Neurol 1988; 24: 181 Tsui JK, Wong NLM, Wong E, et al. Production of circulating antibodies to botulinum-A toxin in patients receiving repeated injections for dystonia. Ann Neurol 1988; 24: 181
171.
Zurück zum Zitat Doellgast GJ, Triscott MX, Beard GA, et al. Sensitive enzyme-linked immunosorbent assay for detection of Clostridium botulinum neurotoxins A, B, and E using signal amplification via enzyme-linked coagulation assay. J Clin Microbiol 1993; 31: 2402–9PubMed Doellgast GJ, Triscott MX, Beard GA, et al. Sensitive enzyme-linked immunosorbent assay for detection of Clostridium botulinum neurotoxins A, B, and E using signal amplification via enzyme-linked coagulation assay. J Clin Microbiol 1993; 31: 2402–9PubMed
172.
Zurück zum Zitat Doellgast GJ, Beard GA, Bottoms JD, et al. Enzyme-linked immunosorbent assay and enzyme-linked coagulation assay for detection of Clostridium botulinum neurotoxin-A, neuro-toxin-B, and neurotoxin-E and solution-phase complexes with dual-label antibodies. J Clin Microbiol 1994; 32: 105–11PubMed Doellgast GJ, Beard GA, Bottoms JD, et al. Enzyme-linked immunosorbent assay and enzyme-linked coagulation assay for detection of Clostridium botulinum neurotoxin-A, neuro-toxin-B, and neurotoxin-E and solution-phase complexes with dual-label antibodies. J Clin Microbiol 1994; 32: 105–11PubMed
173.
Zurück zum Zitat Siatkowski RM, Tyutyunikov A, Biglan AW, et al. Serum antibody production to botulinum-A toxin. Ophthalmology 1993; 100: 1861–6PubMed Siatkowski RM, Tyutyunikov A, Biglan AW, et al. Serum antibody production to botulinum-A toxin. Ophthalmology 1993; 100: 1861–6PubMed
174.
Zurück zum Zitat Hanna PA, Jankovic J. Mouse bioassay versus Western blot assay for botulinum toxin antibodies: correlation with clinical response. Neurology 1998; 50: 1624–9PubMedCrossRef Hanna PA, Jankovic J. Mouse bioassay versus Western blot assay for botulinum toxin antibodies: correlation with clinical response. Neurology 1998; 50: 1624–9PubMedCrossRef
175.
Zurück zum Zitat Greene PE, Fahn S. Use of botulinum toxin type-F injections to treat torticollis in patients with immunity to botulinum toxin type-A. Mov Disord 1993; 8: 479–83PubMedCrossRef Greene PE, Fahn S. Use of botulinum toxin type-F injections to treat torticollis in patients with immunity to botulinum toxin type-A. Mov Disord 1993; 8: 479–83PubMedCrossRef
176.
Zurück zum Zitat Greene PE, Fahn S. Response to botulinum toxin f in seronegative botulinum toxin a — resistant patients. Mov Disord 1996; 11: 181–4PubMedCrossRef Greene PE, Fahn S. Response to botulinum toxin f in seronegative botulinum toxin a — resistant patients. Mov Disord 1996; 11: 181–4PubMedCrossRef
177.
Zurück zum Zitat Ludlow CL, Hallett M, Rhew K, et al. Therapeutic use of type F botulinum toxin [letter]. N Engl J Med 1992; 326: 349–50PubMedCrossRef Ludlow CL, Hallett M, Rhew K, et al. Therapeutic use of type F botulinum toxin [letter]. N Engl J Med 1992; 326: 349–50PubMedCrossRef
178.
Zurück zum Zitat Rhew K, Ludlow CL, Karp BI, et al. Clinical experience with botulinum toxin F. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994: 323–8 Rhew K, Ludlow CL, Karp BI, et al. Clinical experience with botulinum toxin F. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994: 323–8
179.
Zurück zum Zitat Sheean GL, Lees AJ. Botulinum toxin F in the treatment of torticollis clinically resistant to botulinum toxin A. J Neurol Neurosurg Psychiatry 1995; 59: 601–7PubMedCrossRef Sheean GL, Lees AJ. Botulinum toxin F in the treatment of torticollis clinically resistant to botulinum toxin A. J Neurol Neurosurg Psychiatry 1995; 59: 601–7PubMedCrossRef
180.
Zurück zum Zitat Houser MK, Sheean GL, Lees AJ. Further studies using higher doses of botulinum toxin type F for torticollis resistant to botulinum toxin type A. J Neurol Neurosurg Psychiatry 1998; 64: 577–80PubMedCrossRef Houser MK, Sheean GL, Lees AJ. Further studies using higher doses of botulinum toxin type F for torticollis resistant to botulinum toxin type A. J Neurol Neurosurg Psychiatry 1998; 64: 577–80PubMedCrossRef
181.
Zurück zum Zitat Truong DD, Cullis PA, Obrien CF, et al. BotB (botulinum toxin type B): evaluation of safety and tolerability in botulinum toxin type A-resistant cervical dystonia patients (preliminary study). Mov Disord 1997; 12(5): 772–5PubMedCrossRef Truong DD, Cullis PA, Obrien CF, et al. BotB (botulinum toxin type B): evaluation of safety and tolerability in botulinum toxin type A-resistant cervical dystonia patients (preliminary study). Mov Disord 1997; 12(5): 772–5PubMedCrossRef
182.
Zurück zum Zitat Tsui JKC, Hayward M, Mak EKM, et al. Botulinum toxin type B in the treatment of cervical dystonia: a pilot study. Neurology 1995; 45: 2109–10PubMedCrossRef Tsui JKC, Hayward M, Mak EKM, et al. Botulinum toxin type B in the treatment of cervical dystonia: a pilot study. Neurology 1995; 45: 2109–10PubMedCrossRef
183.
Zurück zum Zitat Brin MF, Lew MF, Adler CH, et al. Safety and efficacy of Neurobloc (botulinum toxin type-B) in type-A resistant cervical dystonia (CD) patients. Neurology 1999; 52 Suppl. 2: A293 Brin MF, Lew MF, Adler CH, et al. Safety and efficacy of Neurobloc (botulinum toxin type-B) in type-A resistant cervical dystonia (CD) patients. Neurology 1999; 52 Suppl. 2: A293
184.
Zurück zum Zitat Cullis PA, O’Brien CF, Truong DD, et al. Botulinum toxin type B: an open-label, dose-escalation, safety and preliminary efficacy study in cervical dystonia patients. Adv Neurol 1998; 78: 227–30PubMed Cullis PA, O’Brien CF, Truong DD, et al. Botulinum toxin type B: an open-label, dose-escalation, safety and preliminary efficacy study in cervical dystonia patients. Adv Neurol 1998; 78: 227–30PubMed
185.
Zurück zum Zitat Hatheway CL, Dang C. Immunogenicity of the neurotoxins of Clostridium botulinum. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994; 93–107 Hatheway CL, Dang C. Immunogenicity of the neurotoxins of Clostridium botulinum. In: Jankovic J, Hallett M, editors. Therapy with botulinum toxin. New York: Marcel Dekker, 1994; 93–107
186.
Zurück zum Zitat Dodel RC, Kirchner A, Koehne-Volland R, et al. Costs of treating dystonias and hemifacial spasm with botulinum toxin A. Pharmacoeconomics 1997; 12: 695–706PubMedCrossRef Dodel RC, Kirchner A, Koehne-Volland R, et al. Costs of treating dystonias and hemifacial spasm with botulinum toxin A. Pharmacoeconomics 1997; 12: 695–706PubMedCrossRef
187.
Zurück zum Zitat Goschel H, Wohlfarth K, Frevert J, et al. Botulinum A toxin therapy: neutralizing and nonneutralizing antibodies — therapeutic consequences. Exp Neurol 1997; 147(1): 96–102PubMedCrossRef Goschel H, Wohlfarth K, Frevert J, et al. Botulinum A toxin therapy: neutralizing and nonneutralizing antibodies — therapeutic consequences. Exp Neurol 1997; 147(1): 96–102PubMedCrossRef
188.
Zurück zum Zitat Aoki R, Merlino G, Spanoyannis AF, et al. BOTOX (botulinum toxin type A) purified neurotoxin complex prepared from the new bulk toxin retains the same preclinical efficacy as the original but with reduced immunogenicity. Neurology 1999; 52 Suppl. 2: A521–A2 Aoki R, Merlino G, Spanoyannis AF, et al. BOTOX (botulinum toxin type A) purified neurotoxin complex prepared from the new bulk toxin retains the same preclinical efficacy as the original but with reduced immunogenicity. Neurology 1999; 52 Suppl. 2: A521–A2
189.
Zurück zum Zitat Racette BA, McGee-Minnich L, Perlmutter JS. Efficacy and safety of a new bulk toxin of botulinum toxin in cervical dystonia: a blinded evaluation. Clin Neuropharm 1999; 22: 337–9 Racette BA, McGee-Minnich L, Perlmutter JS. Efficacy and safety of a new bulk toxin of botulinum toxin in cervical dystonia: a blinded evaluation. Clin Neuropharm 1999; 22: 337–9
190.
Zurück zum Zitat Naumann M, Toyka KV, Mansouri TB, et al. Depletion of neutralising antibodies resensitises a secondary non-responder to botulinum A neurotoxin. J Neurol Neurosurg Psychiatry 1998; 65: 924–7PubMedCrossRef Naumann M, Toyka KV, Mansouri TB, et al. Depletion of neutralising antibodies resensitises a secondary non-responder to botulinum A neurotoxin. J Neurol Neurosurg Psychiatry 1998; 65: 924–7PubMedCrossRef
191.
Zurück zum Zitat Duane DD, Monroe J, Morris RE. Mycophenolate in the prevention of recurrent neutralizing botulinum toxin A antibodies in cervical dystonia. Mov Disord 2000; 15(2): 365–6PubMedCrossRef Duane DD, Monroe J, Morris RE. Mycophenolate in the prevention of recurrent neutralizing botulinum toxin A antibodies in cervical dystonia. Mov Disord 2000; 15(2): 365–6PubMedCrossRef
192.
Zurück zum Zitat Ansved T, Odergren T, Borg K. Muscle fiber atrophy in leg muscles after botulinum toxin type A treatment of cervical dystonia. Neurology 1997; 48: 1440–2PubMedCrossRef Ansved T, Odergren T, Borg K. Muscle fiber atrophy in leg muscles after botulinum toxin type A treatment of cervical dystonia. Neurology 1997; 48: 1440–2PubMedCrossRef
193.
Zurück zum Zitat Sanders DB, Massey EW, Buckley EG. Botulinum toxin for blepharospasm: single-fiber EMG studies. Neurology 1986; 36: 545–7PubMedCrossRef Sanders DB, Massey EW, Buckley EG. Botulinum toxin for blepharospasm: single-fiber EMG studies. Neurology 1986; 36: 545–7PubMedCrossRef
194.
Zurück zum Zitat Lange DJ, Warner C, Brin MF, et al. Botulinum toxin therapy: distant effects on neuromuscular transmission [abstract]. Muscle Nerve 1985; 8: 624 Lange DJ, Warner C, Brin MF, et al. Botulinum toxin therapy: distant effects on neuromuscular transmission [abstract]. Muscle Nerve 1985; 8: 624
195.
Zurück zum Zitat Girlanda P, Vita G, Nicolosi C. Botulinum toxin therapy: distant effects on neuromuscular transmission and autonomic nervous system. J Neurol Neurosurg Psychiatry 1992; 55: 844–5PubMedCrossRef Girlanda P, Vita G, Nicolosi C. Botulinum toxin therapy: distant effects on neuromuscular transmission and autonomic nervous system. J Neurol Neurosurg Psychiatry 1992; 55: 844–5PubMedCrossRef
196.
Zurück zum Zitat Scott AB. Clostridial toxins as therapeutic agents. In: Simpson LL, editor. Botulinum neurotoxin and tetanus toxin. New York: Academic Press, 1989: 399–412CrossRef Scott AB. Clostridial toxins as therapeutic agents. In: Simpson LL, editor. Botulinum neurotoxin and tetanus toxin. New York: Academic Press, 1989: 399–412CrossRef
197.
Zurück zum Zitat Moser E, Ligon KM, Singer C, et al. Botulinum toxin A (Botox) therapy during pregnancy [abstract]. Neurology 1997; 48: A399CrossRef Moser E, Ligon KM, Singer C, et al. Botulinum toxin A (Botox) therapy during pregnancy [abstract]. Neurology 1997; 48: A399CrossRef
198.
Zurück zum Zitat Emerson J. Botulinum toxin for spasmodic torticollis in a patient with myasthenia gravis. Mov Disord 1994; 9: 367CrossRef Emerson J. Botulinum toxin for spasmodic torticollis in a patient with myasthenia gravis. Mov Disord 1994; 9: 367CrossRef
199.
Zurück zum Zitat Mezaki T, Kaji R, Kohara N, et al. Development of general weakness in a patient with amyotrophic lateral sclerosis after focal botulinum toxin injection. Neurology 1996; 46: 845–6PubMed Mezaki T, Kaji R, Kohara N, et al. Development of general weakness in a patient with amyotrophic lateral sclerosis after focal botulinum toxin injection. Neurology 1996; 46: 845–6PubMed
200.
Zurück zum Zitat Erbguth F, Claus D, Engelhardt A, et al. Systemic effect of local botulinum toxin injections unmasks subclinical Lambert-Eaton myasthenic syndrome. J Neurol Neurosurg Psychiatry 1993; 56: 1235–6PubMedCrossRef Erbguth F, Claus D, Engelhardt A, et al. Systemic effect of local botulinum toxin injections unmasks subclinical Lambert-Eaton myasthenic syndrome. J Neurol Neurosurg Psychiatry 1993; 56: 1235–6PubMedCrossRef
201.
Zurück zum Zitat Tuite PJ, Lang AE. Severe and prolonged dysphagia complicating botulinum toxin A injections for dystonia in Machado-Joseph disease. Neurology 1996; 46: 846PubMed Tuite PJ, Lang AE. Severe and prolonged dysphagia complicating botulinum toxin A injections for dystonia in Machado-Joseph disease. Neurology 1996; 46: 846PubMed
202.
Zurück zum Zitat Ruiz PJG, Bernardos VS. Intramuscular phenol injection for severe cervical dystonia. J Neurol 2000; 247(2): 146–7CrossRef Ruiz PJG, Bernardos VS. Intramuscular phenol injection for severe cervical dystonia. J Neurol 2000; 247(2): 146–7CrossRef
203.
Zurück zum Zitat Koman LA, Mooney JF III, Smith BP. Neuromuscular blockade in the management of cerebral palsy. J Child Neurol 1996; 11 Suppl. 1: S23–8PubMed Koman LA, Mooney JF III, Smith BP. Neuromuscular blockade in the management of cerebral palsy. J Child Neurol 1996; 11 Suppl. 1: S23–8PubMed
204.
Zurück zum Zitat Bodine-Fowler SC, Allsing S, Botte MJ. Time course of muscle atrophy and recovery following a phenol-induced nerve block. Muscle Nerve 1996; 19: 497–504PubMedCrossRef Bodine-Fowler SC, Allsing S, Botte MJ. Time course of muscle atrophy and recovery following a phenol-induced nerve block. Muscle Nerve 1996; 19: 497–504PubMedCrossRef
205.
Zurück zum Zitat Poemnyi FA, Barsukova MD, Gutorova I. [Treatment of spastic torticollis with phenol-glycerin and alcohol-novocaine blockade]. Zh Nevropatol Psikhiatr Im S S Korsakova 1976; 76: 1326–30PubMed Poemnyi FA, Barsukova MD, Gutorova I. [Treatment of spastic torticollis with phenol-glycerin and alcohol-novocaine blockade]. Zh Nevropatol Psikhiatr Im S S Korsakova 1976; 76: 1326–30PubMed
206.
Zurück zum Zitat Massey JM. Treatment of spasmodic torticollis with intramuscular phenol injection [letter]. J Neurol Neurosurg Psychiatry 1995; 58: 258–9PubMedCrossRef Massey JM. Treatment of spasmodic torticollis with intramuscular phenol injection [letter]. J Neurol Neurosurg Psychiatry 1995; 58: 258–9PubMedCrossRef
207.
Zurück zum Zitat Bertrand C, Molina Negro P, Bouvier G, et al. Observations and analysis of results in 131 cases of spasmodic torticollis after selective denervation. Appl Neurophysiol 1987; 50: 319–23PubMed Bertrand C, Molina Negro P, Bouvier G, et al. Observations and analysis of results in 131 cases of spasmodic torticollis after selective denervation. Appl Neurophysiol 1987; 50: 319–23PubMed
208.
Zurück zum Zitat Bertrand CM. Selective peripheral denervation for spasmodic torticollis: surgical technique, results, and observations in 260 cases. Surg Neurol 1993; 40: 96–103PubMedCrossRef Bertrand CM. Selective peripheral denervation for spasmodic torticollis: surgical technique, results, and observations in 260 cases. Surg Neurol 1993; 40: 96–103PubMedCrossRef
209.
Zurück zum Zitat Cooper IS. Effects of thalamic lesions on torticollis. N Engl J Med 1964; 270: 967–72CrossRef Cooper IS. Effects of thalamic lesions on torticollis. N Engl J Med 1964; 270: 967–72CrossRef
210.
Zurück zum Zitat Hassler R, Dieckmann G. Stereotactic treatment of different kinds of spasmodic torticollis. Confin Neurol 1970; 32: 135–43PubMedCrossRef Hassler R, Dieckmann G. Stereotactic treatment of different kinds of spasmodic torticollis. Confin Neurol 1970; 32: 135–43PubMedCrossRef
211.
Zurück zum Zitat Bertrand CM. The treatment of spasmodic torticollis with particular reference to thalamotomy. In: Mortley T, editor. Current controversies in neurosurgery. Philadelphia: WB Saunders, 1976: 455–9 Bertrand CM. The treatment of spasmodic torticollis with particular reference to thalamotomy. In: Mortley T, editor. Current controversies in neurosurgery. Philadelphia: WB Saunders, 1976: 455–9
212.
Zurück zum Zitat Bertrand CM, Molina-Negro P, Martinez SN. Stereotactic targets for dystonias and dyskinesias: relationship to corticobulbar fibers and other adjoining structures. Adv Neurol 1979; 24: 395–9 Bertrand CM, Molina-Negro P, Martinez SN. Stereotactic targets for dystonias and dyskinesias: relationship to corticobulbar fibers and other adjoining structures. Adv Neurol 1979; 24: 395–9
213.
Zurück zum Zitat Bertrand C, Molina-Negro P, Martinez SN. Combined stereo-tactic and peripheral surgical approach for spasmodic torticollis. Appl Neurophysiol 1978; 41: 122–33PubMed Bertrand C, Molina-Negro P, Martinez SN. Combined stereo-tactic and peripheral surgical approach for spasmodic torticollis. Appl Neurophysiol 1978; 41: 122–33PubMed
214.
Zurück zum Zitat Bertrand C, Molina NP, Martinez SN. Technical aspects of selective peripheral denervation for spasmodic torticollis. Appl Neurophysiol 1982; 45: 326–30PubMed Bertrand C, Molina NP, Martinez SN. Technical aspects of selective peripheral denervation for spasmodic torticollis. Appl Neurophysiol 1982; 45: 326–30PubMed
215.
Zurück zum Zitat Bertrand CM. Stereotactic and peripheral surgery for the control ov movement disorders. In: Barbeau A, editor. Disorders of movements: current status of modern therapy. Lancaster: MTP Press, 1981: 191–208 Bertrand CM. Stereotactic and peripheral surgery for the control ov movement disorders. In: Barbeau A, editor. Disorders of movements: current status of modern therapy. Lancaster: MTP Press, 1981: 191–208
216.
Zurück zum Zitat Bertrand CM, Molina Negro P. Selective peripheral denervation in 111 cases of spasmodic torticollis: rationale and results. Adv Neurol 1988; 50: 637–43PubMed Bertrand CM, Molina Negro P. Selective peripheral denervation in 111 cases of spasmodic torticollis: rationale and results. Adv Neurol 1988; 50: 637–43PubMed
217.
Zurück zum Zitat Arce C, Russo L. Selective peripheral denervation: a surgical alternative in the treatment of spasmodic torticollis. Review of fifty five patients. Mov Disord 1992; 7: 128 Arce C, Russo L. Selective peripheral denervation: a surgical alternative in the treatment of spasmodic torticollis. Review of fifty five patients. Mov Disord 1992; 7: 128
218.
Zurück zum Zitat Davis DH, Ahlskog JE, Litchy WJ, et al. Selective peripheral denervation for torticollis: preliminary results. Mayo Clin Proc 1991; 66: 365–71PubMedCrossRef Davis DH, Ahlskog JE, Litchy WJ, et al. Selective peripheral denervation for torticollis: preliminary results. Mayo Clin Proc 1991; 66: 365–71PubMedCrossRef
219.
Zurück zum Zitat Bertrand CM, Benabou R. Surgical treatment of spasmodic torticollis: selective peripheral denervation revisited. In: Germano I, editor. Neurosurgical treatment of movement disorders. Park Ridge: American Association of Neurological Surgeons, 1998: 239–54 Bertrand CM, Benabou R. Surgical treatment of spasmodic torticollis: selective peripheral denervation revisited. In: Germano I, editor. Neurosurgical treatment of movement disorders. Park Ridge: American Association of Neurological Surgeons, 1998: 239–54
220.
Zurück zum Zitat Bertrand CM, Lenz FA. Surgical treatment of dystonias. In: Tsui JKC, Calne DB, editors. Handbook of dystonia, vol. 39. New York; Marcel Dekker, 1995: 329–46 Bertrand CM, Lenz FA. Surgical treatment of dystonias. In: Tsui JKC, Calne DB, editors. Handbook of dystonia, vol. 39. New York; Marcel Dekker, 1995: 329–46
221.
Zurück zum Zitat Benabou R, Molina-Negro P, Bouvier G. Selection criteria for selective peripheral denervation for spasmodic torticollis. Can J Neurol Sci 1995; 22: S26 Benabou R, Molina-Negro P, Bouvier G. Selection criteria for selective peripheral denervation for spasmodic torticollis. Can J Neurol Sci 1995; 22: S26
222.
Zurück zum Zitat Krauss JK, Toups EG, Jankovic J, et al. Symptomatic and functional outcome of surgical treatment of cervical dystonia. J Neurol Neurosurg Psychiatry 1997; 63(5): 642–8PubMedCrossRef Krauss JK, Toups EG, Jankovic J, et al. Symptomatic and functional outcome of surgical treatment of cervical dystonia. J Neurol Neurosurg Psychiatry 1997; 63(5): 642–8PubMedCrossRef
223.
Zurück zum Zitat Braun V, Richter HP. Selective peripheral denervation for the treatment of spasmodic torticollis. Neurosurgery 1994; 35: 58–62PubMedCrossRef Braun V, Richter HP. Selective peripheral denervation for the treatment of spasmodic torticollis. Neurosurgery 1994; 35: 58–62PubMedCrossRef
224.
Zurück zum Zitat Ford B, Louis ED, Greene P, et al. Outcome of selective ramisectomy for botulinum toxin resistant torticollis. J Neurol Neurosurg Psychiatry 1998; 65: 472–8PubMedCrossRef Ford B, Louis ED, Greene P, et al. Outcome of selective ramisectomy for botulinum toxin resistant torticollis. J Neurol Neurosurg Psychiatry 1998; 65: 472–8PubMedCrossRef
225.
Zurück zum Zitat McKenzie KG. Intrameningeal division of the spinal accessory roots of the upper cervical nerves for the treatment of spasmodic torticollis. Surg Gynecol Obstet 1924; 39: 5–10 McKenzie KG. Intrameningeal division of the spinal accessory roots of the upper cervical nerves for the treatment of spasmodic torticollis. Surg Gynecol Obstet 1924; 39: 5–10
226.
Zurück zum Zitat Dandy WE. An operation for the treatment of spasmodic torticollis. Arch Surg 1930; 20: 1021–32CrossRef Dandy WE. An operation for the treatment of spasmodic torticollis. Arch Surg 1930; 20: 1021–32CrossRef
227.
Zurück zum Zitat Adams CB. Spasmodic torticollis resulting from neurovascular compression. J Neurosurg 1987; 66: 635PubMed Adams CB. Spasmodic torticollis resulting from neurovascular compression. J Neurosurg 1987; 66: 635PubMed
228.
Zurück zum Zitat Freckmann N, Hagenah R, Herrmann HD, et al. Bilateral microsurgical lysis of the spinal accessory nerve roots for treatment of spasmodic torticollis. Follow up of 33 cases. Acta Neurochir 1986; 83: 47–53 Freckmann N, Hagenah R, Herrmann HD, et al. Bilateral microsurgical lysis of the spinal accessory nerve roots for treatment of spasmodic torticollis. Follow up of 33 cases. Acta Neurochir 1986; 83: 47–53
229.
Zurück zum Zitat Adams CB. Vascular catastrophe following the Dandy McKenzie operation for spasmodic torticollis. J Neurol Neurosurg Psychiatry 1984; 47: 990–4PubMedCrossRef Adams CB. Vascular catastrophe following the Dandy McKenzie operation for spasmodic torticollis. J Neurol Neurosurg Psychiatry 1984; 47: 990–4PubMedCrossRef
230.
Zurück zum Zitat Friedman AH, Nashold BS, Sharp R, et al. Treatment of spasmodic torticollis with intradural selective rhizotomies. J Neurosurg 1993; 78: 46–53PubMedCrossRef Friedman AH, Nashold BS, Sharp R, et al. Treatment of spasmodic torticollis with intradural selective rhizotomies. J Neurosurg 1993; 78: 46–53PubMedCrossRef
231.
Zurück zum Zitat Hamby WB, Schiffer S. Spasmodic torticollis; results after cervical rhizotomy in 50 cases. J Neurosurg 1969; 31: 323–6PubMedCrossRef Hamby WB, Schiffer S. Spasmodic torticollis; results after cervical rhizotomy in 50 cases. J Neurosurg 1969; 31: 323–6PubMedCrossRef
232.
Zurück zum Zitat Hamby WB, Schiffer S. Spasmodic torticollis; results after cervical rhizotomy in 80 cases. Clin Neurosurg 1970; 17: 28–37PubMed Hamby WB, Schiffer S. Spasmodic torticollis; results after cervical rhizotomy in 80 cases. Clin Neurosurg 1970; 17: 28–37PubMed
233.
Zurück zum Zitat Perot PL. Upper cervical ventral rhizotomy and selective section of spinal accessory rootlets for spasmodic torticollis. In: Wilson CB, editor. Neurosurgical procedures: personal approaches to classic operations. Baltimore: Williams & Wilkins, 1992: 163–8 Perot PL. Upper cervical ventral rhizotomy and selective section of spinal accessory rootlets for spasmodic torticollis. In: Wilson CB, editor. Neurosurgical procedures: personal approaches to classic operations. Baltimore: Williams & Wilkins, 1992: 163–8
234.
Zurück zum Zitat Shima F, Fukui M, Kitamura K, et al. Diagnosis and surgical treatment of spasmodic torticollis of 1 lth nerve origin. Neurosurgery 1988; 22: 358–63PubMedCrossRef Shima F, Fukui M, Kitamura K, et al. Diagnosis and surgical treatment of spasmodic torticollis of 1 lth nerve origin. Neurosurgery 1988; 22: 358–63PubMedCrossRef
235.
Zurück zum Zitat Jho HD, Jannetta PJ. Microvascular decompression for spasmodic torticollis. Acta Neurochir (Wien) 1995; 134: 21–6CrossRef Jho HD, Jannetta PJ. Microvascular decompression for spasmodic torticollis. Acta Neurochir (Wien) 1995; 134: 21–6CrossRef
236.
Zurück zum Zitat Tasker RR. Outcome after stereotactic thalamotomy for dystonia and hemiballismus — comment. Neurosurgery 1995; 36: 507–8 Tasker RR. Outcome after stereotactic thalamotomy for dystonia and hemiballismus — comment. Neurosurgery 1995; 36: 507–8
237.
Zurück zum Zitat Tasker RR, Doorly T, Yamashiro K. Thalamotomy in generalized dystonia. Adv Neurol 1988; 50: 615–32PubMed Tasker RR, Doorly T, Yamashiro K. Thalamotomy in generalized dystonia. Adv Neurol 1988; 50: 615–32PubMed
238.
Zurück zum Zitat Gros C, Frerebeau P, Perez-Dominguez E, et al. Long term results of stereotaxic surgery for infantile dystonia and dyskinesia. Neurochirurgia Stuttg 1976; 19: 171–8PubMed Gros C, Frerebeau P, Perez-Dominguez E, et al. Long term results of stereotaxic surgery for infantile dystonia and dyskinesia. Neurochirurgia Stuttg 1976; 19: 171–8PubMed
239.
Zurück zum Zitat Caracalos A. Results of 103 cryosurgical procedures in involuntary movement disorders. Confin Neurol 1972; 34: 74–83PubMedCrossRef Caracalos A. Results of 103 cryosurgical procedures in involuntary movement disorders. Confin Neurol 1972; 34: 74–83PubMedCrossRef
240.
Zurück zum Zitat Cooper IM, Bravo GM. Alleviation of dystonia musculorum deformans and other involuntary movement disorders of childhood by chemopallidectomy and chemopallido-thalamectomy. Clin Neurosurg 1958; 5: 127–49 Cooper IM, Bravo GM. Alleviation of dystonia musculorum deformans and other involuntary movement disorders of childhood by chemopallidectomy and chemopallido-thalamectomy. Clin Neurosurg 1958; 5: 127–49
241.
Zurück zum Zitat Vitek JL, Zhang J, Evatt M, et al. GPi pallidotomy for dystonia: clinical outcome and neuronal activity. Adv Neurol 1998; 78: 211–9PubMed Vitek JL, Zhang J, Evatt M, et al. GPi pallidotomy for dystonia: clinical outcome and neuronal activity. Adv Neurol 1998; 78: 211–9PubMed
242.
Zurück zum Zitat Iacono RP, Kuniyoshi SM, Lonser RR, et al. Simultaneous bilateral pallidoansotomy for idiopathic dystonia musculorum deformans. Pediatr Neurol 1996; 14: 145–8PubMedCrossRef Iacono RP, Kuniyoshi SM, Lonser RR, et al. Simultaneous bilateral pallidoansotomy for idiopathic dystonia musculorum deformans. Pediatr Neurol 1996; 14: 145–8PubMedCrossRef
243.
Zurück zum Zitat Shima F, Sakata S, Sun S-J, et al. The role of the descending pallido-reticular pathway in movement disorders. In: Segawa M, Nomura Y, editors. Age-related dopamine-dependent disorders, vol. 14. New York: Karger, 1995: 197–207 Shima F, Sakata S, Sun S-J, et al. The role of the descending pallido-reticular pathway in movement disorders. In: Segawa M, Nomura Y, editors. Age-related dopamine-dependent disorders, vol. 14. New York: Karger, 1995: 197–207
244.
Zurück zum Zitat Islekel S, Zileli M, Zileli B. Unilateral pallidal stimulation in cervical dystonia. Stereotact Funct Neurosurg 1999; 72: 248–52PubMedCrossRef Islekel S, Zileli M, Zileli B. Unilateral pallidal stimulation in cervical dystonia. Stereotact Funct Neurosurg 1999; 72: 248–52PubMedCrossRef
245.
Zurück zum Zitat Krauss JK, Pohle T, Weber S, et al. Bilateral stimulation of globus pallidus internus for treatment of cervical dystonia [letter]. Lancet 1999; 354: 837–8PubMed Krauss JK, Pohle T, Weber S, et al. Bilateral stimulation of globus pallidus internus for treatment of cervical dystonia [letter]. Lancet 1999; 354: 837–8PubMed
Metadaten
Titel
Cervical Dystonia
Pathophysiology and Treatment Options
verfasst von
Dr Miodrag Velickovic
Reina Benabou
Mitchell F. Brin
Publikationsdatum
01.11.2001
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 13/2001
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200161130-00004

Weitere Artikel der Ausgabe 13/2001

Drugs 13/2001 Zur Ausgabe

Adis Drug Evaluation

Cyclosporin