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CADASIL presenting with a movement disorder: A clinical study of a Chilean kindred
(2006)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary vascular disease that usually begins with migraine, followed by repeated strokes and progressive dementia. ...
NOTCH3 gene mutation in a chilean cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy family
(Elsevier, 2020)
Introduction: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary stroke disorder caused by mutations in the NOTCH3 gene. We report the first Chilean ...
CADASIL presenting study with a movement disorder: A clinical of a Chilean kindred
(WILEY-LISS, DIV JOHN WILEY & SONS INC, 2006-07)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary vascular disease that usually begins with migraine, followed by repeated strokes and progressive dementia. ...
Cognitive performance in asymptomatic carriers of mutations R1031C and R141C in CADASILDesempeño cognitivo en portadores asintomáticos de las mutaciones R1031C y R141C en CADASIL
(Editorial BonaventurianaPsicologíaMedellín, 2018)
Mendelian Genes and Risk of Intracerebral Hemorrhage and Small-Vessel Ischemic Stroke in Sporadic Cases
(2017-08)
Background and Purpose—Mendelian strokes are rare genetic disorders characterized by early-onset small-vessel stroke. Although extensively studied among families with syndromic features, whether these genes affect risk ...