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Neurology
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All Genetics

Citations 111-120 of 676 total displayed.

Past content (since Jan 2001):

ARTICLES
Neuropathy progression in Charcot-Marie-Tooth disease type 1A
M. E. Shy, L. Chen, E. R. Swan, R. Taube, K. M. Krajewski, D. Herrmann, R. A. Lewis, and M. P. McDermott
Neurology 2008; 70: 378-383. [Abstract] [Full text] [PDF]  

EDITORIALS
MS and cognition and APOE: The ongoing conundrum about biomarkers
A. Dessa Sadovnick and Daniel H. Jacobs
Neurology 2008; 70: 164-165. [Full text] [PDF]  

ARTICLES
APOE {varepsilon}4 allele is associated with cognitive impairment in patients with multiple sclerosis
J. Shi, C. B. Zhao, T. L. Vollmer, T. M. Tyry, and S. M. Kuniyoshi
Neurology 2008; 70: 185-190. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA
T. Obi, K. Nishioka, O. A. Ross, T. Terada, K. Yamazaki, A. Sugiura, M. Takanashi, K. Mizoguchi, H. Mori, Y. Mizuno, and N. Hattori
Neurology 2008; 70: 238-241. [Full text] [PDF]  

ARTICLES
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation
I. Sato, S. Wu, M. C. A. Ibarra, Y. K. Hayashi, H. Fujita, M. Tojo, S. J. Oh, I. Nonaka, S. Noguchi, and I. Nishino
Neurology 2008; 70: 114-122. [Abstract] [Full text] [PDF]  

VIEWS AND REVIEWS
Genetics of familial amyotrophic lateral sclerosis
Paul N. Valdmanis and Guy A. Rouleau
Neurology 2008; 70: 144-152. [Abstract] [Full text] [PDF]  

EDITORIALS
{alpha}-Synuclein gene duplications in sporadic Parkinson disease
Jessie Theuns and Christine Van Broeckhoven
Neurology 2008; 70: 7-9. [Full text] [PDF]  

ARTICLES
{alpha}-Synuclein gene duplication is present in sporadic Parkinson disease
T. -B. Ahn, S. Y. Kim, J. Y. Kim, S. -S. Park, D. S. Lee, H. J.. Min, Y. K. Kim, S. E. Kim, J. -M. Kim, H. -J. Kim, J. Cho, and B. S. Jeon
Neurology 2008; 70: 43-49. [Abstract] [Full text] [PDF]  

ARTICLES
A structural basis for reading fluency: White matter defects in a genetic brain malformation
B. S. Chang, T. Katzir, T. Liu, K. Corriveau, M. Barzillai, K. A. Apse, A. Bodell, D. Hackney, D. Alsop, S. Wong, and C. A. Walsh
Neurology 2007; 69: 2146-2154. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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