Ausgabe 2/2005
Inhalt (9 Artikel)
LGI1: a gene involved in epileptogenesis and glioma progression?
W. Gu, E. Brodtkorb, T. Piepoli, G. Finocchiaro, O. K. Steinlein
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine
R. A. Lea, D. R. Nyholt, R. P. Curtain, M. Ovcaric, R. Sciascia, C. Bellis, J. MacMillan, S. Quinlan, R. A. Gibson, L. C. McCarthy, J. H. Riley, Y. J. Smithies, S. Kinrade, L. R. Griffiths
Diagnosis of Pelizaeus–Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR
Stefano Regis, Serena Grossi, Susanna Lualdi, Roberta Biancheri, Mirella Filocamo
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia
Johanna A. Reed, Phillip A. Wilkinson, Heema Patel, Michael A. Simpson, Arnaud Chatonnet, Dimitri Robay, Michael A. Patton, Andrew H. Crosby, Thomas T. Warner
Novel mutations and repeated findings of mutations in familial Alzheimer disease
Ulrich Finckh, Christian Kuschel, Maria Anagnostouli, Efstratios Patsouris, George V. Pantes, Stylianos Gatzonis, Elisabeth Kapaki, Panagiota Davaki, Katrin Lamszus, Dimitrios Stavrou, Andreas Gal
Novel G335V mutation in the tau gene associated with early onset familial frontotemporal dementia
Manuela Neumann, Silvia Diekmann, Uwe Bertsch, Ben Vanmassenhove, Bernhard Bogerts, Hans A. Kretzschmar
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene
Bjarne Krebs, Rosa-Maria Lederer, Otto Windl, Eva-Maria Grasbon-Frodl, Inga Zerr, Hans A. Kretzschmar
Screening of the regulatory and coding regions of vascular endothelial growth factor in amyotrophic lateral sclerosis
Alice Brockington, Janine Kirby, Dean Eggitt, Emma Schofield, Chris Morris, Claire E. Lewis, Paul G. Ince, Pamela J. Shaw
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease
Silvia Bagnoli, Andrea Tedde, Elena Cellini, Mario Rotondi, Benedetta Nacmias, Sandro Sorbi