Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy

scientific article published in April 2005

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1097/01.DAD.0000136691.96212.EC
P698PubMed publication ID15798438

P2093author name stringAtsushi Shimizu
Eiichiro Nagata
Kouichi Ohta
Masaru Tanaka
Akira Ishiko
P433issue2
P921main subjectcerebrovascular diseaseQ3010352
P304page(s)131-134
P577publication date2005-04-01
P1433published inAmerican Journal of DermatopathologyQ15754884
P1476titleCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy
P478volume27

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cites work (P2860)
Q43158412A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
Q37694369CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.
Q37789495Cognitive impairment of vascular origin: Neuropathology of cognitive impairment of vascular origin
Q48227491Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.
Q37808273Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.
Q36156335Subcortical ischemic vascular dementia

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