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Neurogenetics
Citations 71-80 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: Implication of Additional Loci
- Joseph H. Lee; Rong Cheng; Neill Graff-Radford; Tatiana Foroud; Richard Mayeux; for the National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group
Arch Neurol 2008; 65: 1518-1526.
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- Neurological Reviews
Friedreich Ataxia
- Massimo Pandolfo
Arch Neurol 2008; 65: 1296-1303.
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- Original Contributions
Development of a High-Throughput Microarray-Based Resequencing System for Neurological Disorders and Its Application to Molecular Genetics of Amyotrophic Lateral Sclerosis
- Yuji Takahashi; Naomi Seki; Hiroyuki Ishiura; Jun Mitsui; Takashi Matsukawa; Atsushi Kishino; Osamu Onodera; Masashi Aoki; Nobuyuki Shimozawa; Shigeo Murayama; Yasuto Itoyama; Yasuyuki Suzuki; Gen Sobue; Masatoyo Nishizawa; Jun Goto; Shoji Tsuji
Arch Neurol 2008; 65: 1326-1332.
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- Original Contributions
Mutations of the ANG Gene in French Patients With Sporadic Amyotrophic Lateral Sclerosis
- Agathe Paubel; Jeremy Violette; Maïté Amy; Julien Praline; Vincent Meininger; William Camu; Philippe Corcia; Christian R. Andres; Patrick Vourc’h; for the French Amyotrophic Lateral Sclerosis (ALS) Study Group
Arch Neurol 2008; 65: 1333-1336.
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- Original Contributions
The Spectrum of Parkinsonian Manifestations Associated With Glucocerebrosidase Mutations
- Ozlem Goker-Alpan; Grisel Lopez; Joseph Vithayathil; Joie Davis; Mark Hallett; Ellen Sidransky
Arch Neurol 2008; 65: 1353-1357.
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- Original Contributions
Association of GSK3B With Alzheimer Disease and Frontotemporal Dementia
- Barbara A. J. Schaffer; Lars Bertram; Bruce L. Miller; Kristina Mullin; Sandra Weintraub; Nancy Johnson; Eileen H. Bigio; Marsel Mesulam; Martina Wiedau-Pazos; George R. Jackson; Jeffrey L. Cummings; Rita M. Cantor; Allan I. Levey; Rudolph E. Tanzi; Daniel H. Geschwind
Arch Neurol 2008; 65: 1368-1374.
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- Observations
Myoclonus-Dystonia Due to Maternal Uniparental Disomy
- Émilie Guettard; Marie-France Portnoi; Katja Lohmann-Hedrich; Boris Keren; Sylvie Rossignol; Susen Winkler; Imen El Kamel; Smaranda Leu; Emmanuelle Apartis; Marie Vidailhet; Christine Klein; Emmanuel Roze
Arch Neurol 2008; 65: 1380-1385.
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- Original Contributions
Two German Kindreds With Familial Amyotrophic Lateral Sclerosis Due to TARDBP Mutations
- Peter Kühnlein; Anne-Dorte Sperfeld; Ben Vanmassenhove; Vivianna Van Deerlin; Virginia M.-Y. Lee; John Q. Trojanowski; Hans A. Kretzschmar; Albert C. Ludolph; Manuela Neumann
Arch Neurol 2008; 65: 1185-1189.
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- Observations
Variable Expression of HPRT Deficiency in 5 Members of a Family With the Same Mutation
- Uros Hladnik; William L. Nyhan; Matteo Bertelli
Arch Neurol 2008; 65: 1240-1243.
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- Original Contributions
Embryonic Myosin Heavy-Chain Mutations Cause Distal Arthrogryposis and Developmental Myosin Myopathy That Persists Postnatally
- Homa Tajsharghi; Eva Kimber; Anna-Karin Kroksmark; Ragnar Jerre; Mar Tulinius; Anders Oldfors
Arch Neurol 2008; 65: 1083-1090.
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