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Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.International Journal of Stroke : Official Journal of the International Stroke Society|February 25, 2009
A double-blind, placebo-controlled, randomized, multicenter study to investigate CHInese Medicine Neuroaid Efficacy on Stroke recovery (CHIMES Study)N Venketasubramanian, C L H Chen, R N Gan, et al.Cephalalgia : an International Journal of Headache|August 14, 2009
Proposals for new standardized general diagnostic criteria for the secondary headachesJ Olesen, T Steiner, M-G Bousser, et al.Cephalalgia : an International Journal of Headache|May 12, 2006
New appendix criteria open for a broader concept of chronic migraine, J Olesen, M-G Bousser, et al.Lancet (London, England)|February 26, 2008
Comparison of idraparinux with vitamin K antagonists for prevention of thromboembolism in patients with atrial fibrillation: a randomised, open-label, non-inferiority trial, M G Bousser, J Bouthier, et al.American Journal of Human Genetics|January 23, 1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxiaA Ducros, C Denier, A Joutel, et al.Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.Nature|October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiaA Joutel, C Corpechot, A Ducros, et al.Pageof 25