Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
about
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patientsCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyA gene for familial hemiplegic migraine maps to chromosome 19Dilation of Virchow-Robin spaces in CADASILBiochemical characterization and cellular effects of CADASIL mutants of NOTCH3De novo mutation in theNotch3 gene causing CADASILImpairments in Episodic-Autobiographical Memory and Emotional and Social Information Processing in CADASIL during Mid-AdulthoodCADASIL: a review with proposed diagnostic criteria.CADASIL and CARASIL.Complications of migraine: migrainous infarction.Role of electron microscopy in the diagnosis of cadasil syndrome: a study of 32 patientsNeuropsychiatric manifestations in CADASIL.Early white matter changes in CADASIL: evidence of segmental intramyelinic oedema in a pre-clinical mouse modelNew phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway.Animal models of ischemic stroke. Part one: modeling risk factors.The pathobiology of vascular malformations: insights from human and model organism genetics.Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease.Lessons from CADASIL.The small leucine-rich proteoglycan BGN accumulates in CADASIL and binds to NOTCH3Multimodal retinal vessel analysis in CADASIL patients.Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome).CADASIL: what component of the vessel wall is really a target for Notch 3 gene mutations?Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalPhysiology and pathology of notch signalling system.CADASIL: a critical look at a Notch disease.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish.Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.Genetics of stroke: a review of recent advances.CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.CADASIL: two new cases with intracerebral hemorrhage.Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature.Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.Notch and disease: a growing field.Headache in stroke: a review.Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Glycohistochemical characterization of vascular muscle cell destruction in CADASIL subjects by lectins, neoglycoconjugates and galectin-specific antibodies.Worsening neurologic deficits in a pilot
P2860
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P2860
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@en
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@nl
type
label
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@en
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@nl
prefLabel
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@en
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@nl
P2093
P356
P1433
P1476
Autosomal dominant leukoenceph ...... . A clinicopathological study.
@en
P2093
E Tournier-Lasserve
M Baudrimont
M G Bousser
P304
P356
10.1161/01.STR.24.1.122
P407
P577
1993-01-01T00:00:00Z