Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 351-360 of 623 total displayed.

Past content

Original Contributions
Effect of MDR1 Haplotype on Risk of Parkinson Disease

Eng-King Tan; Daniel Kam-Yin Chan; Ping-Wing Ng; Jean Woo; Y. Y. Teo; Kun Tang; Li-Peng Wong; Samuel S. Chong; Chris Tan; Hui Shen; Yi Zhao; Caroline G. L. Lee
Arch Neurol 2005; 62: 460-464. [Abstract] [Full text] [PDF]  

Observations
Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF

Ali B. Naini; Jiesheng Lu; Petra Kaufmann; Richard A. Bernstein; Michelangelo Mancuso; Eduardo Bonilla; Michio Hirano; Salvatore DiMauro
Arch Neurol 2005; 62: 473-476. [Abstract] [Full text] [PDF]  

Neurological Reviews
Mouse Models of Human Neurodegenerative Disorders: Requirements for Medication Development

Floyd E. Bloom; John F. Reilly; Jeff M. Redwine; Chi-Cheng Wu; Warren G. Young; John H. Morrison
Arch Neurol 2005; 62: 185-187. [Abstract] [Full text] [PDF]  

Neurological Reviews
Defining Molecular Targets to Prevent Alzheimer Disease

Dennis J. Selkoe
Arch Neurol 2005; 62: 192-195. [Extract] [Full text] [PDF]  

Original Contributions
Blood Gene Expression Profiling of Neurologic Diseases: A Pilot Microarray Study

Yang Tang; Donald L. Gilbert; Tracy A. Glauser; Andrew D. Hershey; Frank R. Sharp
Arch Neurol 2005; 62: 210-215. [Abstract] [Full text] [PDF]  

Original Contributions
Genomic Discovery Reveals a Molecular System for Resistance to Oxidative and Endoplasmic Reticulum Stress in Cultured Glioma

Hassan M. Fathallah-Shaykh
Arch Neurol 2005; 62: 233-236. [Abstract] [Full text] [PDF]  

Observations
A Novel Intronic Mutation in the DDP1 Gene in a Family With X-linked Dystonia-Deafness Syndrome

Mario Ezquerra; Jaume Campdelacreu; Esteban Muñoz; Eduardo Tolosa; María J. Martí
Arch Neurol 2005; 62: 306-308. [Abstract] [Full text] [PDF]  

Observations
Adult Onset Metachromatic Leukodystrophy Without Electroclinical Peripheral Nervous System Involvement: A New Mutation in the ARSA Gene

Ana M. Marcão; Roland Wiest; Kaspar Schindler; Ulrich Wiesmann; Joachim Weis; Gerhard Schroth; Maria Clara S. Miranda; Matthias Sturzenegger; Volkmar Gieselmann
Arch Neurol 2005; 62: 309-313. [Abstract] [Full text] [PDF]  

Observations
Two Novel CACNA1A Gene Mutations Associated With Episodic Ataxia Type 2 and Interictal Dystonia

Sian D. Spacey; Luke A. Materek; Blajez I. Szczygielski; Thomas D. Bird
Arch Neurol 2005; 62: 314-316. [Abstract] [Full text] [PDF]  

Neurological Reviews
Muscle Carnitine Palmitoyltransferase II Deficiency: Clinical and Molecular Genetic Features and Diagnostic Aspects

Marcus Deschauer; Thomas Wieser; Stephan Zierz
Arch Neurol 2005; 62: 37-41. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page] Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63