Ausgabe 4/2008
Inhalt (30 Artikel)
Subgroups of the BENEFIT study: Risk of developing MS and treatment effect of interferon beta-1b
C. Polman, L. Kappos, M. S. Freedman, G. Edan, H.-P. Hartung, D. H. Miller, X. Montalbán, F. Barkhof, K. Selmaj, B. M. J. Uitdehaag, S. Dahms, L. Bauer, C. Pohl*, R. Sandbrink*
Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration
Albert Lladó, Raquel Sánchez-Valle, Maria Jesús Rey, Mario Ezquerra, Eduardo Tolosa, Isidro Ferrer, José Luis Molinuevo
“Pseudodominant inheritance” of ataxia with ocular apraxia type 2 (AOA2)
L. Schöls, L. Arning, R. Schüle, J. T. Epplen, D. Timmann
Severity of explicit memory impairment due to Alzheimer’s disease improves effectiveness of implicit learning
A. Klimkowicz-Mrowiec, A. Slowik, L. Krzywoszanski, R. Herzog-Krzywoszanska, A. Szczudlik
Thrombomodulin gene polymorphisms in brain infarction and mortality after stroke
J.-M. Olivot, J. Labreuche, T. De Broucker, O. Poirier, F. Cambien, M. Aiach, P. Amarenco
Cerebral blood flow abnormality in patients with idiopathic generalized epilepsy
E. Y. Joo, W. S. Tae, S. B. Hong
Cidofovir in combination with HAART and survival in AIDS-associated progressive multifocal leukoencephalopathy
C. Kraemer, S. Evers, T. Nolting, G. Arendt, I. W. Husstedt
Signs of impaired selective attention in patients with amyotrophic lateral sclerosis
E. H. Pinkhardt, R. Jürgens, W. Becker, M. Mölle, J. Born, A. C. Ludolph, H. Schreiber
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration
D. Galimberti, E. Venturelli, C. Fenoglio, I. Guidi, C. Villa, L. Bergamaschini, F. Cortini, D. Scalabrini, P. Baron, C. Vergani, N. Bresolin, E. Scarpini
Botulinum toxin type-B improves sialorrhea and quality of life in bulbaronset amyotrophic lateral sclerosis
J. Costa, M. L. Rocha, J. Ferreira, T. Evangelista, M. Coelho, M. de Carvalho
Radiosurgery of brain arteriovenous malformations in children
D. R. Buis, C. M. F. Dirven, F. J. Lagerwaard, E. S. Mandl, G. J. Lycklama á Nijeholt, D. S. Eshghi, R. van den Berg, J. C. Baayen, O. W. M. Meijer, B. J. Slotman, W. P. Vandertop
Cortical thickness abnormality in juvenile myoclonic epilepsy
W. S. Tae, S. H. Kim, E. Y. Joo, S. J. Han, I. Y. Kim, S. I. Kim, J.-M. Lee, S. B. Hong
Volumetric MRI and cognitive measures in Alzheimer disease
B. H. Ridha, V. M. Anderson, J. Barnes, R. G. Boyes, S. L. Price, M. N. Rossor, J. L. Whitwell, L. Jenkins, R. S. Black, M. Grundman, N. C. Fox
18F-FDG PET in neurodegenerative Langerhans cell histiocytosis
M.-J. Ribeiro, A. Idbaih, C. Thomas, P. Remy, N. Martin-Duverneuil, Y. Samson, J. Donadieu, K. Hoang-Xuan
Extensive cortical inflammation is associated with epilepsy in multiple sclerosis
M. Calabrese, N. De Stefano, M. Atzori, V. Bernardi, I. Mattisi, L. Barachino, L. Rinaldi, A. Morra, M. M. J. McAuliffe, P. Perini, L. Battistin, P. Gallo
Thalidomide causes sinus bradycardia in ALS
T. Meyer, A. Maier, N. Borisow, J. S. Dullinger, G. Splettstößer, S. Ohlraun, C. Münch, P. Linke
Increased MS relapse rate during assisted reproduction technique
K. Hellwig, C. Beste, N. Brune, A. Haghikia, T. Müller, S. Schimrigk, R. Gold
Paraneoplastic Opsoclonus-Myoclonus-Ataxia (OMA) syndrome in an adult patient with esthesioneuroblastoma
D. Van Diest, H. De Raeve, J. Claes, P. M. Parizel, D. De Ridder, P. Cras
Intracerebral hemorrhage caused by cerebral amyloid angiopathy in a 53-year-old man
D. M. Campbell, S. Bruins, H. Vogel, L. M. Shuer, C. A. C. Wijman
Cerebral ultrasound perfusion imaging in a migraine attack with prolonged aura
W. Marouf, A. Hetzel, M. Reinhard, W.-D. Niesen
Transverse venous sinus stenosis and intracranial hypertension: evidence for which comes first
R. Simister, J. V. Bowler, P. L. Wilson, B. Unwin, D. Kidd
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism
L. Bernardi, C. Tomaino, M. Anfossi, M. Gallo, S. Geracitano, G. Puccio, R. Colao, F. Frangipane, M. Mirabelli, N. Smirne, R. Giovanni Maletta, A. C. Bruni
Subarachnoid haemorrhage as the first clinical manifestation of Churg-Strauss syndrome
U.-M. Sheerin, J. Barreto, M. M. Brown, S. Brew, N. A. Losseff
Unique PABPN1 gene mutation in a large Bulgarian family with OPMD
V. Mihaylova, T. Müller, I. Petrova, I. Tournev, S. Cherninkova, M. C. Walter, M. Deschauer
Spinocerebellar ataxia type 4 and 16q22.1-linked Japanese ataxia are not allelic
Y. Hellenbroich, V. Bernard, C. Zühlke
Parkinson's disease: PET studies, neural stem cells and an adenosine receptor antagonist
Michael Strupp