Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
about
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domainCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome).CADASIL: a critical look at a Notch disease.The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China.Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantTargeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients.Genetics of stroke.Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASILNeoplastic lesions in CADASIL syndrome: report of an autopsied Japanese case.Small artery dementia in Japan: radiological differences between CADASIL, leukoaraiosis and Binswanger's disease.Headache among CADASIL patients with R544C mutation: prevalence, characteristics, and associations.First report of a Romanian CADASIL patient following immigration to Italy.Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.Cerebral arteriolar pathology in a 32-year-old patient with CADASIL.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.
P2860
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P2860
Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Genetic, clinical and patholog ...... neration for the pathogenesis.
@en
Genetic, clinical and patholog ...... neration for the pathogenesis.
@nl
type
label
Genetic, clinical and patholog ...... neration for the pathogenesis.
@en
Genetic, clinical and patholog ...... neration for the pathogenesis.
@nl
prefLabel
Genetic, clinical and patholog ...... neration for the pathogenesis.
@en
Genetic, clinical and patholog ...... neration for the pathogenesis.
@nl
P2093
P1476
Genetic, clinical and patholog ...... neration for the pathogenesis.
@en
P2093
De Hua Chui
Eiichiro Uyama
Keikichi Takahashi
Masakuni Arima
Satoshi Kotorii
Takeshi Tabira
P356
10.1016/S0022-510X(03)00109-6
P577
2003-08-01T00:00:00Z