Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.
about
Cerebral small vessel disease and Alzheimer's diseaseMicrovascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brainGenetics of subcortical vascular dementiaGenetics of age-related white matter lesions from linkage to genome wide association studiesAge and the metabolic syndrome as risk factors for ischemic stroke: improving preclinical models of ischemic strokeWhite Matter Lesion Progression: Genome-Wide Search for Genetic InfluencesCommon variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel diseaseNOTCH3 variants and risk of ischemic stroke.Cerebral 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.Longitudinal change of small-vessel disease-related brain abnormalitiesCardiovascular risk factors and small vessel disease of the brain: Blood pressure, white matter lesions, and functional decline in older personsStroke genetics: a review and update.Genetics of cerebral small vessel diseaseCommon NOTCH3 Variants and Cerebral Small-Vessel Disease.R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.Association of Notch3 single-nucleotide polymorphisms and lacunar infarctions in patients.Stroke injury, cognitive impairment and vascular dementiaUp-regulation of serotonin receptor 2B mRNA and protein in the peri-infarcted area of aged rats and stroke patients.Immunolocalization of platelet-derived growth factor receptor-β (PDGFR-β) and pericytes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL.Neurovascular signaling in the brain and the pathological consequences of hypertension.Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging.Small vessel disease and memory loss: what the clinician needs to know to preserve patients' brain health.Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.Monogenic causes of stroke: now and the future.Genetics of ischaemic stroke.Prognostic value of Notch receptors in postsurgical patients with hepatitis B virus-related hepatocellular carcinoma.Combined effects of age and polymorphisms in Notch3 in the pathogenesis of cerebral infarction disease.A population neuroscience approach to the study of cerebral small vessel disease in mid- and late-life: an Invited Review.Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3.
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P2860
Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@ast
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@en
type
label
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@ast
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@en
prefLabel
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@ast
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@en
P2093
P2860
P50
P356
P1433
P1476
Genetic variants of the NOTCH3 ...... cerebral small vessel disease.
@en
P2093
CHARGE consortium Neurology working group
Christian Enzinger
Katja Petrovic
Marco Wiltgen
Margherita Cavalieri
Marion Zeginigg
Paul Freudenberger
Pierre Gider
Reinhold Schmidt
Stephanie Debette
P2860
P304
P356
10.1093/BRAIN/AWR252
P407
P577
2011-10-17T00:00:00Z