Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 521-530 of 623 total displayed.

Past content

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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