Zobrazeno 1 - 10
of 195
pro vyhledávání: '"R. J. Uitti"'
Autor:
R. A. Gross, D. S. Knopman, A. A. Amato, G. D. Cascino, O. Ciccarelli, J. R. Corboy, M. S. V. Elkind, J. W. Mink, R. M. Ransohoff, R. J. Uitti, B. B. Worrall
Publikováno v:
Neurology. 83:4-12
Autor:
R. A. Gross, D. S. Knopman, G. D. Cascino, J. R. Corboy, M. S. V. Elkind, A. G. Engel, J. W. Mink, R. M. Ransohoff, R. J. Uitti, B. B. Worrall
Publikováno v:
Neurology. 79:5-12
Autor:
J. H. Noseworthy, R. A. Gross, A. G. Engel, K. C. Johnston, D. S. Knopman, J. W. Mink, R. M. Ransohoff, R. J. Uitti
Publikováno v:
Neurology. 75:2-9
Autor:
R. A. Gross, D. S. Knopman, G. D. Cascino, M. S. V. Elkind, A. G. Engel, J. W. Mink, R. M. Ransohoff, R. J. Uitti, B. B. Worrall
Publikováno v:
Neurology. 72:2-7
Autor:
J. H. Noseworthy, R. A. Gross, A. G. Engel, K. C. Johnston, D. S. Knopman, R. M. Ransohoff, R. J. Uitti
Publikováno v:
Neurology. 70:92-96
Publikováno v:
Neurology. 75:1943-1945
{#article-title-2} To The Editor: The recent exchange between Drs. Ahlskog and Uitti1 and Drs. Olanow and Rascol2 regarding the ADAGIO study demonstrates a curious paradox in our professional debates. Research trials intended to affect patient care m
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 77:1235-1237
Autor:
J C, Dachsel, C, Wider, C, Vilariño-Güell, J O, Aasly, A, Rajput, A H, Rajput, T, Lynch, D, Craig, A, Krygowska-Wajs, B, Jasinska-Myga, G, Opala, M, Barcikowska, K, Czyzewski, R-M, Wu, M G, Heckman, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 18(8)
Mutations of the LRRK2 gene are now recognized as major risk factors for Parkinson's disease. The Lrrk2 protein is a member of the ROCO family, which also includes Lrrk1 and Dapk1. Functional genetic variants of the DAPK1 gene (rs4877365 and rs487810
Autor:
C, Wider, C, Vilariño-Güell, M G, Heckman, B, Jasinska-Myga, A I, Ortolaza-Soto, N N, Diehl, J E, Crook, S A, Cobb, J A, Bacon, J O, Aasly, J M, Gibson, T, Lynch, R J, Uitti, Z K, Wszolek, M J, Farrer, O A, Ross
Publikováno v:
European journal of neurology. 18(6)
Recent evidence suggests that variation in the SNCA, MAPT, and GSK3B genes interacts in affecting risk for Parkinson disease (PD). In the current study, we attempt to validate previously published findings, evaluating gene-gene interactions between S
Publikováno v:
Neurology. 54:2028-2030