1. Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease

   • Kristin K. Nicodemus
   • Judith E. Stenger
   • Eden R. Martin

   Original Article 29 September 2004 Pages: 201 - 208

   

2. Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

   • Yi-Ju Li
   • Margaret A. Pericak-Vance
   • Teepu Siddique

   Original Article 02 October 2004 Pages: 209 - 213

   

3. Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families

   • Ryuki Hirano
   • Hiroshi Takashima
   • Kimiyoshi Arimura

   Original Article 29 September 2004 Pages: 215 - 221

   

4. Alternative splicing in the N-terminus of Alzheimer’s presenilin 1

   • Wiep Scheper
   • Rob Zwart
   • Frank Baas

   Original Article 05 October 2004 Pages: 223 - 227

   

5. Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse

   • Ashraf U. Mannan
   • Elena Roussa
   • Wolfgang Engel

   Original Article 22 October 2004 Pages: 229 - 238

   

6. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A

   • Annette Abel
   • Nuria Fonknechten
   • Jamilé Hazan

   Original Article 28 October 2004 Pages: 239 - 243

   

7. Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism

   • P. Saccucci
   • M. Verdecchia
   • P. Curatolo

   Original Article 14 October 2004 Pages: 245 - 248

   

8. A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob disease

   • E. Grasbon-Frodl
   • R. Schmalzbauer
   • H. A. Kretzschmar

   Letter to the Editors 05 October 2004 Pages: 249 - 250

   

9. Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene

   • J. Busby
   • K. K. O’Brien
   • C. M. Morris

   Letter to the Editors 14 October 2004 Pages: 251 - 252