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Association studies in genetics
Citations 81-90 of 148 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Correlating phenotype and genotype in the periodic paralyses
- T. M. Miller, M. R. Dias da Silva, H. A. Miller, H. Kwiecinski, J. R. Mendell, R. Tawil, P. McManis, R. C. Griggs, C. Angelini, S. Servidei, J. Petajan, M. C. Dalakas, L. P.W. Ranum, Y. H. Fu, and L. J. Ptácek
Neurology 2004; 63: 1647-1655.
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- BRIEF COMMUNICATIONS
Alcohol dehydrogenase 2 variant is associated with cerebral infarction and lacunae
- Y. Suzuki, M. Fujisawa, F. Ando, N. Niino, I. Ohsawa, H. Shimokata, and S. Ohta
Neurology 2004; 63: 1711-1713.
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- BRIEF COMMUNICATIONS
The –1021C T DBH gene variant is not associated with epilepsy or antiepileptic drug response
- C. Depondt, H. R. Cock, D. G. Healy, M. W. Burley, D. Weinshenker, N. W. Wood, D. B. Goldstein, and S. M. Sisodiya
Neurology 2004; 63: 1497-1499.
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- EXPEDITED BRIEF COMMUNICATION
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache
- I. Rainero, S. Gallone, W. Valfrè, M. Ferrero, G. Angilella, C. Rivoiro, E. Rubino, P. De Martino, L. Savi, M. Ferrone, and L. Pinessi
Neurology 2004; 63: 1286-1288.
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- EDITORIALS
Association of genetic loci: Replication or not, that is the question
- Jurg Ott
Neurology 2004; 63: 955-958.
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- BRIEF COMMUNICATIONS
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy
- F. Zimprich, R. Sunder-Plassmann, E. Stogmann, A. Gleiss, A. Dal-Bianco, A. Zimprich, S. Plumer, C. Baumgartner, and C. Mannhalter
Neurology 2004; 63: 1087-1089.
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- BRIEF COMMUNICATIONS
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy
- N. C.K. Tan, S. E. Heron, I. E. Scheffer, J. T. Pelekanos, J. M. McMahon, D. F. Vears, J. C. Mulley, and S. F. Berkovic
Neurology 2004; 63: 1090-1092.
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- CLINICAL/SCIENTIFIC NOTES
Gene–gene interaction between interleukin-6 and interleukin-10 reduces AD risk
- J. Infante, C. Sanz, J. L. Fernández-Luna, J. Llorca, J. Berciano, and O. Combarros
Neurology 2004; 63: 1135-1136.
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- BRIEF COMMUNICATIONS
Cortical malformations are associated with a rare polymorphism of cellular prion protein
- R. Walz, R. M.R.P.S. Castro, M. C. Landemberger, T. R. Velasco, V. C. Terra-Bustamante, A. C. Bastos, M. Bianchin, L. Wichert-Ana, D. Araújo, V. Alexandre, Jr., A. C. Santos, H. R. Machado, C. G. Carlotti, Jr., R. R. Brentani, V. R. Martins, and A. C. Sakamoto
Neurology 2004; 63: 557-560.
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- ARTICLES
Insulin-degrading enzyme and Alzheimer disease: A genetic association study in the Han Chinese
- L. Bian, J. D. Yang, T. W. Guo, Y. Sun, S. W. Duan, W. Y. Chen, Y. X. Pan, G. Y. Feng, and L. He
Neurology 2004; 63: 241-245.
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