Browsing by Subject "CADASIL"

Now showing items 1-3 of 3

    • CADASIL presenting with a movement disorder: A clinical study of a Chilean kindred 
      Miranda, Marcelo; Dichgans, Martin; Slachevsky Chonchol, Andrea; Urbina, Francisco; Mena, Ismael; Venegas, Pablo; Galvez, Marcelo (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. ...
    • CADASIL: Hereditary vascular dementia. Description of an apparently sporadic clinical case 
      Sáez, David; Trujillo, Osvaldo; Nogales-Gaete, Jorge; Figueroa, Tatiana; Valenzuela, Daniel (2003)
      We describe a patient with CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy), the first of four patients diagnosed in our service since 1998, correlating clinical, imaging, ...
    • NOTCH3 gene mutation in a chilean cerebral autosomal dominant arteriopathy with subcortical infarcts and ... 
      Gallardo Vera, Andrés; Latapiat, Verónica; Rivera, Alejandra; Fonseca, Beatriz; Roldán, Andrés; Sandoval, Patricio; Sánchez, Carolina; Matamala Capponi, José (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 ...