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Neurogenetics
Citations 481-490 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Trinucleotide Repeats in 202 Families With Ataxia: A Small Expanded (CAG)n Allele at the SCA17 Locus
- I. Silveira; C. Miranda; L. Guimarães; M.-C. Moreira; I. Alonso; P. Mendonça; A. Ferro; J. Pinto-Basto; J. Coelho; F. Ferreirinha; J. Poirier; E. Parreira; J. Vale; C. Januário; C. Barbot; A. Tuna; J. Barros; R. Koide; S. Tsuji; S. E. Holmes; R. L. Margolis; L. Jardim; M. Pandolfo; P. Coutinho; J. Sequeiros
Arch Neurol 2002; 59: 623-629.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- Editorials
Genomic Neurology: A New Beginning
- Roger N. Rosenberg
Arch Neurol 2001; 58: 1739-1741.
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