Results 171 to 180 of about 12,711 (284)
Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study [PDF]
Anand Viswanathan
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CADASIL: A NOTCH3-associated cerebral small vessel disease
L. Yuan+3 more
semanticscholar +1 more source
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
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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL [PDF]
Johanna Annunen‐Rasila+8 more
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CADASIL Notch3 Mutant Proteins Localize to the Cell Surface and Bind Ligand
Talin Haritunians+8 more
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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
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