Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
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Endoglin regulates mural cell adhesion in the circulatory systemA Dormant Microbial Component in the Development of PreeclampsiaFunctional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic TelangiectasiaThe use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia.Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans.Central nervous system manganese induced lesions and clinical consequences in patients with hereditary hemorrhagic telangiectasiaALK1 signaling inhibits angiogenesis by cooperating with the Notch pathway.Hereditary hemorrhagic telangiectasia and pregnancy: potential adverse events and pregnancy outcomesBrain arteriovenous malformation modeling, pathogenesis, and novel therapeutic targets.Molecular pathways: can activin-like kinase pathway inhibition enhance the limited efficacy of VEGF inhibitors?Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasiaEndoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia.Fine mapping of the hereditary haemorrhagic telangiectasia (HHT)3 locus on chromosome 5 excludes VE-Cadherin-2, Sprouty4 and other interval genes.Structural and functional insights into endoglin ligand recognition and binding.Bevacizumab in hereditary hemorrhagic telangiectasia-associated epistaxis: effectiveness of an injection protocol based on the vascular anatomy of the nose.Optimal management of hereditary hemorrhagic telangiectasia.Heterozygous deficiency of endoglin decreases insulin and hepatic triglyceride levels during high fat dietLifestyle and dietary influences on nosebleed severity in hereditary hemorrhagic telangiectasia.Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasiaVascular remodeling after ischemic stroke: mechanisms and therapeutic potentialsHemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency.Pulmonary arteriovenous malformations.Copy number variations in endoglin locus: mapping of large deletions in Spanish families with hereditary hemorrhagic telangiectasia type 1.Organ specific optical imaging of mitochondrial redox state in a rodent model of hereditary hemorrhagic telangiectasia-1Ischaemic strokes in patients with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia: associations with iron deficiency and plateletsArterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformationsGenetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14Endothelial depletion of Acvrl1 in mice leads to arteriovenous malformations associated with reduced endoglin expression.Research on potential biomarkers in hereditary hemorrhagic telangiectasia.Bleeding and clotting in hereditary hemorrhagic telangiectasiaCirculatory contributors to the phenotype in hereditary hemorrhagic telangiectasiaBMP9 Crosstalk with the Hippo Pathway Regulates Endothelial Cell Matricellular and Chemokine Responses.Effects of dilution and prolonged storage with preservative in a polyethylene container on Bevacizumab (Avastin™) for topical delivery as a nasal spray in anti-hereditary hemorrhagic telangiectasia and related therapies.5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia.Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within MinutesBrain abscess caused by Enterococcus faecalis following a dental procedure in a patient with hereditary hemorrhagic telangiectasia.Mice Lacking Endoglin in Macrophages Show an Impaired Immune Response.A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective studyMutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1.Vascular Integrity in the Pathogenesis of Brain Arteriovenous Malformation.
P2860
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P2860
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@ast
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@en
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@nl
type
label
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@ast
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@en
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@nl
prefLabel
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@ast
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@en
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@nl
P1433
P1476
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment.
@en
P304
P356
10.1016/J.BLRE.2010.07.001
P577
2010-09-25T00:00:00Z