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Biochemistry|May 16, 2009
Understanding how diverse beta-mannanases recognize heterogeneous substratesLouise E Tailford, Valerie M-A Ducros, James E Flint, 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.Neurology|June 17, 1999
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2C Denier, A Ducros, K Vahedi, et al.American Journal of Human Genetics|January 1, 1996
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalA Ducros, T Nagy, S Alamowitch, et al.European Review for Medical and Pharmacological Sciences|May 18, 2021
Reversible cerebral vasoconstriction syndrome: a comprehensive systematic reviewT-J Song, K H Lee, H Li, et al.Pageof 6