Hereditary haemorrhagic telangiectasia: a clinical analysis.
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Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasiaHereditary haemorrhagic telangiectasia: a clinical and scientific reviewHereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesisRecurrent Gastrointestinal Hemorrhage in Treatment with Dasatinib in a Patient Showing SMAD4 Mutation with Acute Lymphoblastic Leukemia Philadelphia Positive and Juvenile Polyposis Hereditary Hemorrhagic Telangiectasia Syndrome.Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.Update on Clinical Strategies in Hereditary Hemorrhagic Telangiectasia from an ENT Point of View.Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?Endoglin in liver fibrogenesis: Bridging basic science and clinical practiceClinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.Targeting under-diagnosis in hereditary hemorrhagic telangiectasia: a model approach for rare diseases?A woman with an unusual case of hemoptysisRare manifestations in a case of Osler-Weber-Rendu diseaseHereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era.Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.From developmental disorder to heritable cancer: it's all in the BMP/TGF-beta family.Complications and mortality in hereditary hemorrhagic telangiectasia: A population-based study.Hereditary hemorrhagic telangiectasia: an overview of diagnosis and management in the molecular era for clinicians.A rare case of pulmonary arterio-venous malformation with recurrent anemia: Hereditary hemorrhagic telangiectasia.Hereditary benign telangiectasia--first family in Northern IrelandEndoglin: a critical mediator of cardiovascular healthClinical features and mutations in the ENG, ACVRL1, and SMAD4 genes in Korean patients with hereditary hemorrhagic telangiectasia.Hereditary hemorrhagic telangiectasia.Woman presenting with chronic iron deficiency anemia associated with hereditary hemorrhagic telangiectasia: a case report.High-Output Heart Failure Contributing to Recurrent Epistaxis Kiesselbach Area Syndrome in a Patient With Hereditary Hemorrhagic Telangiectasia.Hereditary hemorrhagic telangiectasia patients can tolerate anticoagulation.A review of vascular anomalies: genetics and common syndromes.TGF-β & BMP receptors endoglin and ALK1: overview of their functional role and status as antiangiogenic targets.Screening for arteriovenous malformations in hereditary haemorrhagic telangiectasia.Epistaxis grading in Osler's disease: comparison of comprehensive scores with detailed bleeding diaries.Endoglin-based biological therapy in the treatment of angiogenesis-dependent pathologies.Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients.Combined juvenile polyposis and hereditary hemorrhagic telangiectasiaGastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient.Clinical and analytical sensitivities in hereditary hemorrhagic telangiectasia testing and a report of de novo mutationsThe UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study.Depression and post-traumatic stress disorder in individuals with hereditary hemorrhagic telangiectasia: A cross-sectional survey.Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasia.Living with hereditary haemorrhagic telangiectasia: coping and psychological distress - a cross-sectional study.
P2860
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P2860
Hereditary haemorrhagic telangiectasia: a clinical analysis.
description
1992 nî lūn-bûn
@nan
1992 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@ast
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@en
type
label
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@ast
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@en
prefLabel
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@ast
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@en
P2093
P2860
P356
P1476
Hereditary haemorrhagic telangiectasia: a clinical analysis.
@en
P2093
P2860
P304
P356
10.1136/JMG.29.8.527
P407
P577
1992-08-01T00:00:00Z