neurogenetics 4/2004

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Inhaltsverzeichnis ( 9 Artikel )

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Original Article | Ausgabe 4/2004

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

Wiep Scheper, Rob Zwart, Frank Baas

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Original Article | Ausgabe 4/2004

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

01.12.2004 | Letter to the Editors | Ausgabe 4/2004

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

01.12.2004 | Letter to the Editors | Ausgabe 4/2004

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

neurogenetics

Ausgabe 4/2004

Inhaltsverzeichnis ( 9 Artikel )

Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease

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

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

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

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

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

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

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

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

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Springer Medizin

Inhaltsverzeichnis ( 9 Artikel )

Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease

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

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

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

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

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

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

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

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

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