COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
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Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiencyGene-environment interactions in severe intraventricular hemorrhage of preterm neonatesGenetic Risk Factors for Ischemic and Hemorrhagic StrokePhenotypic spectrum of COL4A1 mutations: porencephaly to schizencephalyCommon variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel diseaseCerebral small vessel disease: insights and opportunities from mouse models of collagen IV-related small vessel disease and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.Personalized management of atrial fibrillation: Proceedings from the fourth Atrial Fibrillation competence NETwork/European Heart Rhythm Association consensus conference.The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literature.Imaging of Cerebral Microbleeds.Peroxidasin is essential for eye development in the mouseStroke genetics: a review and update.Crucial role for the VWF A1 domain in binding to type IV collagen.Molecular and Genetic Analyses of Collagen Type IV Mutant Mouse Models of Spontaneous Intracerebral Hemorrhage Identify Mechanisms for Stroke PreventionER stress and basement membrane defects combine to cause glomerular and tubular renal disease resulting from Col4a1 mutations in mice.COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets.How benign is hematuria? Using genetics to predict prognosis.Genetic risk factors for spontaneous intracerebral haemorrhage.Genotype-phenotype correlations in pathology caused by collagen type IV alpha 1 and 2 mutations.Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population.COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls.Cilostazol ameliorates collagenase-induced cerebral hemorrhage by protecting the blood-brain barrier.Genetic Suppression of Basement Membrane Defects in Caenorhabditis elegans by Gain of Function in Extracellular Matrix and Cell-Matrix Attachment Genes.Genetics of Spontaneous Intracerebral Hemorrhage.Neuroimaging in Dementia.The triple helix of collagens - an ancient protein structure that enabled animal multicellularity and tissue evolution.Brain vascular heterogeneity: implications for disease pathogenesis and design of in vitro blood-brain barrier models.
P2860
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P2860
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@ast
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@en
type
label
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@ast
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@en
prefLabel
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@ast
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@en
P2093
P2860
P356
P1433
P1476
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.
@en
P2093
Akshata Sonni
Alessandro Biffi
Cassandre Labelle-Dumais
Douglas B Gould
Marion Jeanne
Michelle de Leau
Steven M Greenberg
W Berkeley Kauffman
Yi-Chinn Weng
P2860
P304
P356
10.1002/ANA.22682
P577
2012-04-01T00:00:00Z