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Genetic Disorders
Citations 291-300 of 396 total displayed.
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Past content
(since Jan 1998):
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- Neurological Reviews
Friedreich Ataxia: Effects of Genetic Understanding on Clinical Evaluation and Therapy
- David R. Lynch; Jennifer M. Farmer; Laura J. Balcer; Robert B. Wilson
Arch Neurol 2002; 59: 743-747.
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- Original Contributions
Plasma Homocysteine Levels, Cerebrovascular Risk Factors, and Cerebral White Matter Changes (Leukoaraiosis) in Patients With Alzheimer Disease
- Eva Hogervorst; Helen Mendes Ribeiro; Andrew Molyneux; Marc Budge; A. David Smith
Arch Neurol 2002; 59: 787-793.
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- Original Contributions
Contribution of the Interleukin 4 Gene to Susceptibility to Subacute Sclerosing Panencephalitis
- Takehiko Inoue; Ryutaro Kira; Futoshi Nakao; Kenji Ihara; Wafaa M. Bassuny; Koichi Kusuhara; Kenji Nihei; Kenzo Takeshita; Toshiro Hara
Arch Neurol 2002; 59: 822-827.
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- Original Contributions
Familial Aggregation of Parkinson Disease: A Comparative Study of Early-Onset and Late-Onset Disease
- Haydeh Payami; Sepideh Zareparsi; Dora James; John Nutt
Arch Neurol 2002; 59: 848-850.
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- Observations
Cytochrome c Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease
- Leonardo Salviati; Sabrina Sacconi; Minerva M. Rasalan; David F. Kronn; Alex Braun; Peter Canoll; Mercy Davidson; Sara Shanske; Eduardo Bonilla; Arthur P. Hays; Eric A. Schon; Salvatore DiMauro
Arch Neurol 2002; 59: 862-865.
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- Original Contributions
Association Between Apolipoprotein E Genotype and Alzheimer Disease in African American Subjects
- Neill R. Graff-Radford; Robert C. Green; Rodney C. P. Go; Michael L. Hutton; Timi Edeki; David Bachman; Jennifer L. Adamson; Patrick Griffith; Floyd B. Willis; Mary Williams; Yvonne Hipps; Jonathan L. Haines; L. Adrienne Cupples; Lindsay A. Farrer
Arch Neurol 2002; 59: 594-600.
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- Original Contributions
Differences in Tau and Apolipoprotein E Polymorphism Frequencies in Sporadic Frontotemporal Lobar Degeneration Syndromes
- Rodney A. Short; Neill R. Graff-Radford; Jennifer Adamson; Matt Baker; Mike Hutton
Arch Neurol 2002; 59: 611-615.
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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
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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