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Association studies in genetics
Citations 61-70 of 147 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS
- R. Fernández-Santiago, M. Sharma, J. C. Mueller, H. Gohlke, T. Illig, J. Anneser, C. Münch, A. Ludolph, C. Kamm, and T. Gasser
Neurology 2006; 66: 1929-1931.
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- BRIEF COMMUNICATIONS
Strong association of MuSK antibody–positive myasthenia gravis and HLA-DR14-DQ5
- E. H. Niks, J.B.M. Kuks, B. O. Roep, G. W. Haasnoot, W. Verduijn, B. E.P.B. Ballieux, M. H. De Baets, A. Vincent, and J. J.G.M. Verschuuren
Neurology 2006; 66: 1772-1774.
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- BRIEF COMMUNICATIONS
The ICAM-1 E469K gene polymorphism is a risk factor for spontaneous cervical artery dissection
- M. Longoni, C. Grond-Ginsbach, A. J. Grau, J. Genius, S. Debette, M. Schwaninger, C. Ferrarese, and C. Lichy
Neurology 2006; 66: 1273-1275.
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- BRIEF COMMUNICATIONS
Two patients with COMT inhibitor–induced hepatic dysfunction and UGT1A9 genetic polymorphism
- E. Martignoni, M. Cosentino, M. Ferrari, G. Porta, E. Mattarucchi, F. Marino, S. Lecchini, and G. Nappi
Neurology 2005; 65: 1820-1822.
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- BRIEF COMMUNICATIONS
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
- S. Karamohamed, J. C. Latourelle, B. A. Racette, J. S. Perlmutter, G. F. Wooten, M. Lew, C. Klein, H. Shill, L. I. Golbe, M. H. Mark, M. Guttman, G. Nicholson, J. B. Wilk, M. Saint-Hilaire, A. L. DeStefano, R. Prakash, S. Tobin, J. Williamson, O. Suchowersky, N. Labell, B.N.J. Growdon, C. Singer, R. Watts, S. Goldwurm, G. Pezzoli, K. B. Baker, M. L. Giroux, P. P. Pramstaller, D. J. Burn, P. Chinnery, S. Sherman, P. Vieregge, I. Litvan, J. F. Gusella, R. H. Myers, and A. Parsian
Neurology 2005; 65: 1823-1825.
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- ARTICLES
Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population
- M.J.E. van Rijn, A. J.C. Slooter, A. F.C. Schut, A. Isaacs, Y. S. Aulchenko, P. J.L.M. Snijders, L. J. Kappelle, J. C. van Swieten, B. A. Oostra, and C. M. van Duijn
Neurology 2005; 65: 1203-1209.
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- BRIEF COMMUNICATIONS
Analysis of LRRK2 functional domains in nondominant Parkinson disease
- L. Skipper, H. Shen, E. Chua, C. Bonnard, P. Kolatkar, L.C.S. Tan, R. D. Jamora, K. Puvan, K. Y. Puong, Y. Zhao, R. Pavanni, M. C. Wong, Y. Yuen, M. Farrer, J. J. Liu, and E. K. Tan
Neurology 2005; 65: 1319-1321.
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- ARTICLES
IL-1RN and IL-1B gene polymorphisms and cerebral hemorrhagic events after traumatic brain injury
- G. M. Hadjigeorgiou, K. Paterakis, E. Dardiotis, M. Dardioti, K. Aggelakis, A. Tasiou, G. Xiromerisiou, A. Komnos, E. Zintzaras, N. Scarmeas, A. Papadimitriou, and A. Karantanas
Neurology 2005; 65: 1077-1082.
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- CLINICAL/SCIENTIFIC NOTES
Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease
- H. Deng, W. D. Le, Y. Guo, M. S. Huang, W. J. Xie, and J. Jankovic
Neurology 2005; 65: 651-652.
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- BRIEF COMMUNICATIONS
Cystatin C as a risk factor for Alzheimer disease
- H. M. Cathcart, R. Huang, I. S. Lanham, E. H. Corder, and S. E. Poduslo
Neurology 2005; 64: 755-757.
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