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Neurogenetics
Citations 471-480 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Clinical Features and Disease Haplotypes of Individuals With the N279K tau Gene Mutation: A Comparison of the Pallidopontonigral Degeneration Kindred and a French Family
- Yoshio Tsuboi; Ryan J. Uitti; Marie-Bernadette Delisle; Joaquim J. Ferreira; Christine Brefel-Courbon; Olivier Rascol; Bernardino Ghetti; Jill R. Murrell; Michael Hutton; Matthew Baker; Zbigniew K. Wszolek
Arch Neurol 2002; 59: 943-950.
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- Original Contributions
Molecular Findings in Familial Parkinson Disease in Spain
- Janet Hoenicka; Lídice Vidal; Blas Morales; Israel Ampuero; F. Javier Jiménez-Jiménez; Jose Berciano; Teodoro del Ser; Adriano Jiménez; Pedro G. Ruíz; Justo G. de Yébenes
Arch Neurol 2002; 59: 966-970.
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- Observations
Complex Neurologic Syndrome Associated With the G1606A Mutation of Mitochondrial DNA
- Sabrina Sacconi; Leonardo Salviati; Clifton Gooch; Eduardo Bonilla; Sara Shanske; Salvatore DiMauro
Arch Neurol 2002; 59: 1013-1015.
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- Observations
Mutation Analysis of the CACNA1A Calcium Channel Subunit Gene in 27 Patients With Sporadic Hemiplegic Migraine
- Gisela Terwindt; Esther Kors; Joost Haan; Frans Vermeulen; Arn van den Maagdenberg; Rune Frants; Michel Ferrari; for the International Hemiplegic Migraine Research Group
Arch Neurol 2002; 59: 1016-1018.
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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
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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