Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
about
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyExome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseA gene for familial hemiplegic migraine maps to chromosome 19Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12De novo mutation in theNotch3 gene causing CADASILStroke Risk Factors, Genetics, and Prevention.Impairments in Episodic-Autobiographical Memory and Emotional and Social Information Processing in CADASIL during Mid-AdulthoodCADASIL: a review with proposed diagnostic criteria.Neuropsychiatric manifestations in CADASIL.Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneityNew phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureMultiple acute infarcts in the posterior circulation.Functional analysis of a recurrent missense mutation in Notch3 in CADASILCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalPotential confounding by intermediate phenotypes in studies of the genetics of ischaemic stroke.Causes of ischaemic stroke in the young.The enigma of vascular cognitive disorder and vascular dementia.The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China.Clinical variability of the cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in two siblings of a large family showing the same mutationGenetics of ischaemic stroke; single gene disorders.Migraine and stroke: current perspectives.A Notch updated.Headache and cardiovascular disease: old symptoms, new proposals.Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Vascular dementia in Japan.Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease.Detection of the founder effect in Finnish CADASIL families.CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene.Detection of granular osmiophilic material of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy by light microscopy in frozen sections.CADASIL syndrome: a genetic form of vascular dementia.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Neuropathological and in vitro studies of abnormal elastogenesis.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: an imaging mimic of multiple sclerosis. A report of two cases.CADASIL imitating multiple sclerosis: the importance of MRI markers.Clinical, familial, and neuroimaging features of CADASIL-like patients.Pseudomigraine with prolonged aphasia in a child with cranial irradiation for medulloblastoma.Peripheral nerve and skeletal muscle involvement in CADASIL.Update on Vascular Cognitive Impairment Associated with Subcortical Small-Vessel Disease.Cadasil: presenting as a mood disorder.
P2860
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P2860
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh-hant
name
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@en
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@nl
type
label
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@en
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@nl
prefLabel
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@en
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@nl
P2093
P1433
P1476
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.
@en
P2093
E Tournier-Lasserve
M G Bousser
M T Iba-Zizen
P304
P356
10.1161/01.STR.22.10.1297
P407
P577
1991-10-01T00:00:00Z