Hereditary neuralgic amyotrophy Jan MeulemanVincent TimmermanPeter De Jonghe Review Article 16 March 2001 Pages: 115 - 118
Leber hereditary optic neuropathy: clinical and molecular genetic findings Kirsi Huoponen Review Article 16 May 2001 Pages: 119 - 125
Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity Kyproula ChristodoulouFeza DeymeerLefkos T. Middleton Original Article 21 April 2001 Pages: 127 - 132
Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism Joanne LeungChristine KleinXandra O. Breakefield Original Article 19 May 2001 Pages: 133 - 143
Genetic susceptibility to MS: a second stage analysis in Canadian MS families David A. DymentCristen J. WillerGeorge C. Ebers Original Article 16 May 2001 Pages: 145 - 151
EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy Cornelius F. BoerkoelHiroshi TakashimaJames R. Lupski Original Article 15 March 2001 Pages: 153 - 157
Analysis of p53 mutation and expression in pleomorphic xanthoastrocytoma Caterina GianniniDeanne HebrinkCharles D. James Original Article 07 June 2001 Pages: 159 - 162
Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents S. KöselE. Grasbon-FrodlM. Graeber Original Paper 08 May 2001 Pages: 163 - 170
An association between a subset of Finnish late-onsetAlzheimer’s disease and alpha2-macroglobulin M. PirskanenI. AlafuzoffH. Soininen Letter to the Editors 17 March 2001 Pages: 171 - 172
