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Neurology
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Association studies in genetics

Citations 111-120 of 147 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Genetic variation of the APOE promoter and outcome after head injury
C. L. Lendon, J. M. Harris, A. L. Pritchard, J. A.R. Nicoll, G. M. Teasdale, and G. Murray
Neurology 2003; 61: 683-685. [Abstract] [Full text] [PDF]  

ARTICLES
Myelin basic protein gene is associated with MS in DR4- and DR5-positive Italians and Russians
F. R. Guerini, P. Ferrante, L. Losciale, D. Caputo, M. L. Lombardi, G. Pirozzi, V. Luongo, M. A. Sudomoina, T. V. Andreewski, A. D. Alekseenkov, A. N. Boiko, E. I. Gusev, and O. O. Favorova
Neurology 2003; 61: 520-526. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy
R. de Silva, A. Hope, A. Pittman, M.E. Weale, H.R. Morris, N.W. Wood, and A.J. Lees
Neurology 2003; 61: 407-409. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A mutated CCR5 gene may have favorable prognostic implications in MS
Rami Kantor, Mary Bakhanashvili, and Anat Achiron
Neurology 2003; 61: 238-240. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Modulation of the onset age in primary dystonia by APOE genotype
S. Matsumoto, M. Nishimura, T. Sakamoto, K. Asanuma, Y. Izumi, H. Shibasaki, N. Kamatani, T. Nakamura, and R. Kaji
Neurology 2003; 60: 2003-2005. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Early visual function impairment in CADASIL
V. Parisi, F. Pierelli, F. Fattapposta, F. Bianco, L. Parisi, R. Restuccia, A. Malandrini, M. Ferrari, and P. Carrera
Neurology 2003; 60: 2008-2010. [Abstract] [Full text] [PDF]  

ARTICLES
L -Dopa-induced adverse effects in PD and dopamine transporter gene polymorphism
R. Kaiser, A. Hofer, A. Grapengiesser, T. Gasser, A. Kupsch, I. Roots, and J. Brockmöller
Neurology 2003; 60: 1750-1755. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson’s disease
J. M. van der Walt, E.R. Martin, W. K. Scott, F. Zhang, M.A. Nance, R. L. Watts, J. P. Hubble, J. L. Haines, W. C. Koller, K. Lyons, R. Pahwa, M. B. Stern, A. Colcher, B. C. Hiner, J. Jankovic, W. G. Ondo, F. H. Allen, Jr., C. G. Goetz, G. W. Small, F. Mastaglia, A. D. Roses, J. M. Stajich, M.W. Booze, K. Fujiwara, R. A. Gibson, L. T. Middleton, B. L. Scott, M. A. Pericak-Vance, and J. M. Vance
Neurology 2003; 60: 1189-1191. [Abstract] [Full text] [PDF]  

ARTICLES
Strong association between N-acetyltransferase 2 genotype and PD in Hong Kong Chinese
D.K.Y. Chan, M.K.P. Lam, R. Wong, W.T. Hung, and D.E.L. Wilcken
Neurology 2003; 60: 1002-1005. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Possible association of the tau H1/H1 genotype with primary progressive aphasia
M.-J. Sobrido, A. Abu–Khalil, S. Weintraub, N. Johnson, B. Quinn, J. L. Cummings, M.-M. Mesulam, and D. H. Geschwind
Neurology 2003; 60: 862-864. [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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