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Association studies in genetics
Citations 111-120 of 148 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy
- D. Audenaert, L. Claes, B. Ceulemans, A. Löfgren, C. Van Broeckhoven, and P. De Jonghe
Neurology 2003; 61: 854-856.
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- 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.
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- 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.
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- 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.
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- 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.
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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.
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- 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.
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- 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.
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- 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.
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- 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.
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