Results 171 to 180 of about 12,711 (284)

CADASIL: A NOTCH3-associated cerebral small vessel disease

open access: yesJournal of Advanced Research
L. Yuan   +3 more
semanticscholar   +1 more source

First intravenous thrombolysis for pCys194Arg Notch 3 mutation in a Moroccan CADASIL patient with stroke

open access: yesRadiology Case Reports
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene. Clinical manifestations of CADASIL include lacunar infarcts, transient ischemic attacks, dementia, migraine ...
Mohamed Amine Mnaili, MD
doaj  

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL [PDF]

open access: bronze, 2006
Johanna Annunen‐Rasila   +8 more
openalex   +1 more source

CADASIL Notch3 Mutant Proteins Localize to the Cell Surface and Bind Ligand

open access: bronze, 2002
Talin Haritunians   +8 more
openalex   +1 more source

Stem cell factor and granulocyte colony-stimulating factor exhibit therapeutic effects in a mouse model of CADASIL

open access: yesNeurobiology of Disease, 2015
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a Notch3 dominant mutation-induced cerebral small vascular disease, is characterized by progressive degeneration of vascular smooth muscle cells (vSMCs)
Xiao-Yun Liu   +9 more
doaj  

Myocardial Infarction in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)

open access: bronze, 2003
Saskia A.J. Lesnik Oberstein   +7 more
openalex   +1 more source

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