1. Hereditary neuralgic amyotrophy

   • Jan Meuleman
   • Vincent Timmerman
   • Peter De Jonghe

   Review Article 16 March 2001 Pages: 115 - 118

2. Leber hereditary optic neuropathy: clinical and molecular genetic findings

   • Kirsi Huoponen

   Review Article 16 May 2001 Pages: 119 - 125

3. Mapping of the second Friedreich's ataxia (FRDAff2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity

   • Kyproula Christodoulou
   • Feza Deymeer
   • Lefkos T. Middleton

   Original Article 21 April 2001 Pages: 127 - 132

4. Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism

   • Joanne Leung
   • Christine Klein
   • Xandra O. Breakefield

   Original Article 19 May 2001 Pages: 133 - 143

5. Genetic susceptibility to MS: a second stage analysis in Canadian MS families

   • David A. Dyment
   • Cristen J. Willer
   • George C. Ebers

   Original Article 16 May 2001 Pages: 145 - 151

6. EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy

   • Cornelius F. Boerkoel
   • Hiroshi Takashima
   • James R. Lupski

   Original Article 15 March 2001 Pages: 153 - 157

7. Analysis of p53 mutation and expression in pleomorphic xanthoastrocytoma

   • Caterina Giannini
   • Deanne Hebrink
   • Charles D. James

   Original Article 07 June 2001 Pages: 159 - 162

8. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents

   • S. Kösel
   • E. Grasbon-Frodl
   • M. Graeber

   Original Paper 08 May 2001 Pages: 163 - 170

9. An association between a subset of Finnish late-onsetAlzheimer’s disease and alpha₂-macroglobulin

   • M. Pirskanen
   • I. Alafuzoff
   • H. Soininen

   Letter to the Editors 17 March 2001 Pages: 171 - 172