Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL.
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Adult↗
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Results for “CADASIL”
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Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993.
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Cerebral Arterial Diseases↗
CADASIL: Notch signaling defect or protein accumulation problem?
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Brain↗
Retinal vascular abnormalities in CADASIL.
To assess retinal vascular alterations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, the authors examined 10 affected individuals with ophthalmologic evaluation including fluorescence angiography. Findings included bilateral peripapillary arteriolar sheathing (30%), arteriolar narrowing (80%), and arteriovenous nicking (90%). No retinal infarcts, vascular occlusions, exudation, or hypoperfusion of affected vessels were found.
Adult↗
Acetazolamide-responsive migraine in CADASIL.
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Acetazolamide↗
CADASIL in a North American family.
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Brain Diseases↗
Cerebrospinal fluid findings in CADASIL.
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Adult↗
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL.
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Alleles↗
Acetazolamide for the treatment of migraine with aura in CADASIL.
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Acetazolamide↗
Skin biopsy findings in CADASIL.
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Basement Membrane↗
Unusual presentation of CADASIL with reversible coma and confusion.
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Aged↗
Diagnostic strategies in CADASIL.
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Amino Acid Substitution↗
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) characteristics in Japan: variety of clinical features.
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Cerebral Infarction↗
[Identification of Notch 3 mutation in the first Japanese CADASIL family].
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Asian People↗
[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)].
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Cerebral Cortex↗
[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): a new genetic disease of the cerebral arteries associated with vascular leukoencephalopathies].
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Brain↗