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Neurology
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Association studies in genetics

Citations 141-148 of 148 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Apolipoprotein E and age at onset of Alzheimer’s disease in African American patients
F.C. Goldstein, A.V. Ashley, M. Gearing, J. Hanfelt, L. Penix, L.J. Freedman, and A.I. Levey
Neurology 2001; 57: 1923-1925. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Atrial natriuretic peptide gene G664A polymorphism and the risk of ischemic cerebrovascular disease
A. Hassan, N. Ali, Y. Dong, N. D. Carter, and H. S. Markus
Neurology 2001; 57: 1726-1728. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysis
A. Desautels, G. Turecki, J. Montplaisir, N. Ftouhi–Paquin, M. Michaud, V.A. Chouinard, and G.A. Rouleau
Neurology 2001; 57: 1304-1306. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Association of a tumor necrosis factor {alpha} polymorphism with MS susceptibility
Brian G. Weinshenker, David D. Hebrink, Elizabeth Atkinson, and Orhun H. Kantarci
Neurology 2001; 57: 1341-1342. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomas
F. Martinez di Montemuros, D. Tavazzi, E. Salsano, T. Piepoli, B. Pollo, G. Fiorelli, and G. Finocchiaro
Neurology 2001; 57: 1342. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD
G. Savettieri, E. V. De Marco, D. Civitelli, G. Salemi, G. Nicoletti, G. Annesi, I. C. Cirò Candiano, and A. Quattrone
Neurology 2001; 57: 560-561. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities
P. Verpillat, A. Alpérovitch, F. Cambien, V. Besançon, H. Desal, and C. Tzourio
Neurology 2001; 56: 673-675. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A prepro-orexin gene polymorphism is associated with narcolepsy
M. Gencik, N. Dahmen, S. Wieczorek, M. Kasten, J. Bierbrauer, I. Anghelescu, A. Szegedi, A. M. Menezes Saecker, and J. T. Epplen
Neurology 2001; 56: 115-117. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* 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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