Ausgabe 4/2004
Inhalt (9 Artikel)
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease
Kristin K. Nicodemus, Judith E. Stenger, Donald E. Schmechel, Kathleen A. Welsh-Bohmer, Ann M. Saunders, Allen D. Roses, John R. Gilbert, Jeffery M. Vance, Jonathan L. Haines, Margaret A. Pericak-Vance, Eden R. Martin
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis
Yi-Ju Li, Margaret A. Pericak-Vance, Jonathan L. Haines, Nailah Siddique, Diane McKenna-Yasek, Wu-Yen Hung, Peter Sapp, Coy I. Allen, Wenjie Chen, Betsy Hosler, Ann M. Saunders, Lisa M. Dellefave, Robert H. Brown Jr, Teepu Siddique
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families
Ryuki Hirano, Hiroshi Takashima, Ryuichi Okubo, Keiko Tajima, Yuji Okamoto, Shimon Ishida, Kazuhito Tsuruta, Takayo Arisato, Hitoshi Arata, Masanori Nakagawa, Mitsuhiro Osame, Kimiyoshi Arimura
Alternative splicing in the N-terminus of Alzheimer’s presenilin 1
Wiep Scheper, Rob Zwart, Frank Baas
Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse
Ashraf U. Mannan, Elena Roussa, Cornelia Kraus, Micheal Rickmann, Joerg Maenner, Karim Nayernia, Kerstin Krieglstein, André Reis, Wolfgang Engel
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A
Annette Abel, Nuria Fonknechten, Anne Hofer, Alexandra Dürr, Corinne Cruaud, Thomas Voit, Jean Weissenbach, Alexis Brice, Sven Klimpe, Georg Auburger, Jamilé Hazan
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism
P. Saccucci, M. Verdecchia, A. Piciullo, N. Bottini, R. Rizzo, F. Gloria-Bottini, P. Lucarelli, P. Curatolo
A novel three extra-repeat insertion in the prion protein gene (PRNP) in a patient with Creutzfeldt-Jakob disease
E. Grasbon-Frodl, R. Schmalzbauer, P. Weber, B. Krebs, O. Windl, I. Zerr, H. A. Kretzschmar
Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene
J. Busby, K. K. O’Brien, A. M. Gibson, I. G. McKeith, R. H. Perry, J. A. Hardy, A. B. Singleton, C. M. Morris