Results 161 to 170 of about 8,915 (192)

Multiomic profiling reveals pericyte and smooth muscle cell contributions to CADASIL pathology in cell-specific Notch3 mutant mice

open access: yes
Huang Y   +9 more
europepmc   +1 more source

CADASIL

Lancet Neurology, The, 2009
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is the most common heritable cause of stroke and vascular dementia in adults. Clinical and neuroimaging features resemble those of sporadic small-artery disease, although patients with CADASIL have an earlier age at onset of stroke events, an increased ...
Hugues Chabriat   +2 more
exaly   +7 more sources

CADASIL

Journal of Geriatric Psychiatry and Neurology, 2010
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a dominantly inherited small artery disease that leads to dementia and disability in mid-life. The clinical presentation of CADASIL is variable between and within affected families and is characterized by symptoms including migraine with aura ...
D, Hervé, H, Chabriat
openaire   +3 more sources

CADASIL

2018
Cerebral small-vessel disease is a prevalent condition that is strongly associated with ischemic stroke and dementia. The most prevalent inherited cause of cerebral small-vessel disease is CADASIL, cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, a disorder linked to mutations in NOTCH3.
openaire   +2 more sources

CADASIL

Revue Neurologique, 2004
S, Stefanizzi   +3 more
  +5 more sources

CYSTEINE-SPARING NOTCH3 MUTATIONS: CADASIL OR CADASIL VARIANTS?

Neurology, 2008
Copyright (2008) LIPPINCOTT WILLIAMS ...
Scheid, R.   +7 more
openaire   +4 more sources

Pregnancy in CADASIL

Acta Neurologica Scandinavica, 2017
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebral small vessel disease caused by NOTCH3 gene mutations. CADASIL women are frequently considered at high risk of systemic vascular events during pregnancy and often prescribed with antithrombotic drugs.
Donnini, I.   +10 more
openaire   +4 more sources

CADASIL

Advances in Anatomic Pathology, 1998
M. Dichgans, T. Gasser
  +5 more sources

Lessons from CADASIL

Annals of the New York Academy of Sciences, 2002
Abstract: Vascular dementia (VaD) includes several different vascular mechanisms and changes in the brain. Among VaD, CADASIL is an inherited angiopathy caused by mutations in the Notch3 gene. The pathological hallmark of CADASIL is a granular osmiophilic material deposit (GOM) that is not only found in the brain, but also in the peripheral vascular ...
Ruchoux, Marie-Magdeleine   +5 more
openaire   +3 more sources

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