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Genetic Counseling/ Testing/ Therapy
Citations 71-80 of 122 total displayed.
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Past content
(since May 1998):
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- Original Contributions
A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter
- Zoran Brkanac; Laura Bylenok; Magali Fernandez; Mark Matsushita; Hillary Lipe; John Wolff; David Nochlin; Wendy H. Raskind; Thomas D. Bird
Arch Neurol 2002; 59: 1291-1295.
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- Original Contributions
Active Human Herpesvirus 6 Infection in Patients With Multiple Sclerosis
- Roberto Álvarez-Lafuente; Carlos Martín-Estefanía; Virginia de las Heras; Carmen Castrillo; Juan José Picazo; Eduardo Varela de Seijas; Rafael Arroyo González
Arch Neurol 2002; 59: 929-933.
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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
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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- Editorials
Prospects for Vascular Endothelial Growth Factor Neurotherapeutics
- David Pleasure; Peter Bannerman; Jahan Ara; Marina Scarlato; Takayuki Itoh
Arch Neurol 2002; 59: 692-694.
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- Editorials
Darts in the Dark Cure Animal, but Not Human, Brain Tumors
- Hassan M. Fathallah-Shaykh
Arch Neurol 2002; 59: 721-724.
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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
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
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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