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Neurology
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All Genetics

Citations 111-120 of 679 total displayed.

Past content (since Jan 2001):

ARTICLES
Neuropathology of primary adult-onset dystonia
J. L. Holton, S. A. Schneider, T. Ganesharajah, S. Gandhi, C. Strand, P. Shashidharan, J. Barreto, N. W. Wood, A. J. Lees, K. P. Bhatia, and T. Revesz
Neurology 2008; 70: 695-699. [Abstract] [Full text] [PDF]  

ARTICLES
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations
A. S. Chen-Plotkin, W. Yuan, C. Anderson, E. McCarty Wood, H. I. Hurtig, C. M. Clark, B. L. Miller, V. M.-Y. Lee, J. Q. Trojanowski, M. Grossman, and V. M. Van Deerlin
Neurology 2008; 70: 521-527. [Abstract] [Full text] [PDF]  

ARTICLES
Prevalence of SOD1 mutations in the Italian ALS population
A. Chiò, B. J. Traynor, F. Lombardo, M. Fimognari, A. Calvo, P. Ghiglione, R. Mutani, and G. Restagno
Neurology 2008; 70: 533-537. [Abstract] [Full text] [PDF]  

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]  

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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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