Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 531-540 of 623 total displayed.

Past content

Original Contributions
Association of a Null Mutation in the CNTF Gene With Early Onset of Multiple Sclerosis

Ralf Giess; Mathias Mäurer; Ralf Linker; Ralf Gold; Monika Warmuth-Metz; Klaus V. Toyka; Michael Sendtner; Peter Rieckmann
Arch Neurol 2002; 59: 407-409. [Abstract] [Full text] [PDF]  

Original Contributions
Reduced Aquaporin 4 Expression in the Muscle Plasma Membrane of Patients With Duchenne Muscular Dystrophy

Yoshihiro Wakayama; Takahiro Jimi; Masahiko Inoue; Hiroko Kojima; Makoto Murahashi; Toshiyuki Kumagai; Sumimasa Yamashita; Hajime Hara; Seiji Shibuya
Arch Neurol 2002; 59: 431-437. [Abstract] [Full text] [PDF]  

Observations
Unequal Crossing-over in Unique PABP2 Mutations in Japanese Patients: A Possible Cause of Oculopharyngeal Muscular Dystrophy

Mika Nakamoto; Satoshi Nakano; Shingo Kawashima; Masafumi Ihara; Yo Nishimura; Akiyo Shinde; Akira Kakizuka
Arch Neurol 2002; 59: 474-477. [Abstract] [Full text] [PDF]  

Original Contributions
Biochemical-Clinical Correlation in Patients With Different Loads of the Mitochondrial DNA T8993G Mutation

Valerio Carelli; Alessandra Baracca; Silvia Barogi; Francesco Pallotti; Maria Lucia Valentino; Pasquale Montagna; Massimo Zeviani; Antonella Pini; Giorgio Lenaz; Agostino Baruzzi; Giancarlo Solaini
Arch Neurol 2002; 59: 264-270. [Abstract] [Full text] [PDF]  

Original Contributions
Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia

Inge A. Meijer; Collette K. Hand; P. Cossette; Denise A. Figlewicz; Guy A. Rouleau
Arch Neurol 2002; 59: 281-286. [Abstract] [Full text] [PDF]  

Observations
Corneal Endothelial Degeneration in Dentatorubral-Pallidoluysian Atrophy

Daisuke Ito; Masakazu Yamada; Masataka Kawai; Tomohiko Usui; Junnich Hamada; Yasuo Fukuuchi
Arch Neurol 2002; 59: 289-291. [Abstract] [Full text] [PDF]  

Observations
Intrafamilial Phenotypic Variability in Friedreich Ataxia Associated With a G130V Mutation in the FRDA Gene

Dominick J. H. McCabe; Nicholas W. Wood; Fergus Ryan; Michael G. Hanna; Sean Connolly; David P. Moore; Janice Redmond; David E. Barton; Raymond P. Murphy
Arch Neurol 2002; 59: 296-300. [Abstract] [Full text] [PDF]  

Neurological Reviews
Investigating Chemokines and Chemokine Receptors in Patients With Multiple Sclerosis: Opportunities and Challenges

Corinna Trebst; Richard M. Ransohoff
Arch Neurol 2001; 58: 1975-1980. [Abstract] [Full text] [PDF]  

Editorials
Genomic Neurology: A New Beginning

Roger N. Rosenberg
Arch Neurol 2001; 58: 1739-1741. [Extract] [Full text] [PDF]  

Editorials
The Human Genome Is Sequenced: What Does It Mean and Why Is It Important?

John Hardy
Arch Neurol 2001; 58: 1748-1749. [Extract] [Full text] [PDF]  

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