Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease Kristin K. NicodemusJudith E. StengerEden R. Martin Original Article 29 September 2004 Pages: 201 - 208
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis Yi-Ju LiMargaret A. Pericak-VanceTeepu Siddique Original Article 02 October 2004 Pages: 209 - 213
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families Ryuki HiranoHiroshi TakashimaKimiyoshi Arimura Original Article 29 September 2004 Pages: 215 - 221
Alternative splicing in the N-terminus of Alzheimer’s presenilin 1 Wiep ScheperRob ZwartFrank Baas Original Article 05 October 2004 Pages: 223 - 227
Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse Ashraf U. MannanElena RoussaWolfgang Engel Original Article 22 October 2004 Pages: 229 - 238
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A Annette AbelNuria FonknechtenJamilé Hazan Original Article 28 October 2004 Pages: 239 - 243
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism P. SaccucciM. VerdecchiaP. Curatolo Original Article 14 October 2004 Pages: 245 - 248
A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob disease E. Grasbon-FrodlR. SchmalzbauerH. A. Kretzschmar Letter to the Editors 05 October 2004 Pages: 249 - 250
Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene J. BusbyK. K. O’BrienC. M. Morris Letter to the Editors 14 October 2004 Pages: 251 - 252