LGI1: a gene involved in epileptogenesis and glioma progression? W. GuE. BrodtkorbO. K. Steinlein Review Article 13 April 2005 Pages: 59 - 66
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine R. A. LeaD. R. NyholtL. R. Griffiths Original Article 14 April 2005 Pages: 67 - 72
Diagnosis of Pelizaeus–Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCR Stefano RegisSerena GrossiMirella Filocamo Original Article 13 April 2005 Pages: 73 - 78
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia Johanna A. ReedPhillip A. WilkinsonThomas T. Warner Short Communication 12 February 2005 Pages: 79 - 84
Novel mutations and repeated findings of mutations in familial Alzheimer disease Ulrich FinckhChristian KuschelAndreas Gal Short Communication 18 March 2005 Pages: 85 - 89
Novel G335V mutation in the tau gene associated with early onset familial frontotemporal dementia Manuela NeumannSilvia DiekmannHans A. Kretzschmar Letter to the Editors 12 March 2005 Pages: 91 - 95
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene Bjarne KrebsRosa-Maria LedererHans A. Kretzschmar Letter to the Editors 18 March 2005 Pages: 97 - 100
Screening of the regulatory and coding regions of vascular endothelial growth factor in amyotrophic lateral sclerosis Alice BrockingtonJanine KirbyPamela J. Shaw Letter to the Editors 18 March 2005 Pages: 101 - 104
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer’s disease Silvia BagnoliAndrea TeddeSandro Sorbi Erratum 19 March 2005 Pages: 105 - 105