Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 101-110 of 623 total displayed.

Past content

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

Medical News & Perspectives
Academic Medical Centers Embark on Public Outreach Through the Internet

Tracy Hampton
JAMA 2008; 300: 1015. [Extract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

Preliminary Communications
Within-Person Across-Neuropsychological Test Variability and Incident Dementia

Roee Holtzer; Joe Verghese; Cuiling Wang; Charles B. Hall; Richard B. Lipton
JAMA 2008; 300: 823-830. [Abstract] [Full text] [PDF]  

Original Articles
Apolipoprotein E 4 Allele Genotype and the Effect of Depressive Symptoms on the Risk of Dementia in Men: The Honolulu-Asia Aging Study

Fumiko Irie; Kamal H. Masaki; Helen Petrovitch; Robert D. Abbott; G. Webster Ross; Dennis R. Taaffe; Lenore J. Launer; Lon R. White
Arch Gen Psychiatry 2008; 65: 906-912. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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