Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients.
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Embolisation for pulmonary arteriovenous malformationEmbolisation for pulmonary arteriovenous malformationEmbolisation therapy for pulmonary arteriovenous malformationsEmbolisation therapy for pulmonary arteriovenous malformationsHereditary haemorrhagic telangiectasia: a clinical and scientific reviewHereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of diseaseEpistaxis in hereditary hemorrhagic telangiectasia: an evidence based review of surgical management.Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic TelangiectasiaEnhanced responses to angiogenic cues underlie the pathogenesis of hereditary hemorrhagic telangiectasia 2The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia.Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.Mutations in the ALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families.Endoglin and activin receptor-like-kinase 1 are co-expressed in the distal vessels of the lung: implications for two familial vascular dysplasias, HHT and PAH.Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanismsFamilial cerebral abscesses caused by hereditary hemorrhagic telangiectasiaDiagnosis and Treatment of Hereditary Hemorrhagic Telangiectasia.Stroke in hereditary hemorrhagic telangiectasia patients. New evidence for repeated screening and early treatment of pulmonary vascular malformations: two case reportsClinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.Very low dose bevacizumab for the treatment of epistaxis in patients with hereditary hemorrhagic telangiectasia.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.Optimal management of hereditary hemorrhagic telangiectasia.Targeting under-diagnosis in hereditary hemorrhagic telangiectasia: a model approach for rare diseases?Lifestyle 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 telangiectasiaSeverity score for hereditary hemorrhagic telangiectasia.Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic teleangiectasia.Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.Circulating angiogenic cell dysfunction in patients with hereditary hemorrhagic telangiectasiaLong non-coding RNA expression profiles in hereditary haemorrhagic telangiectasia.A postal survey of hereditary hemorrhagic telangectasia in the northeast of EnglandConnective tissue disorders and cardiovascular complications: the indomitable role of transforming growth factor-beta signalingSuccessful treatment of bleeding gastro-intestinal angiodysplasia in hereditary haemorrhagic telangiectasia with thalidomide.Complications and mortality in hereditary hemorrhagic telangiectasia: A population-based study.Neurovascular manifestations in hereditary hemorrhagic telangiectasia: imaging features and genotype-phenotype correlations.Hereditary hemorrhagic telangiectasia: an overview of diagnosis and management in the molecular era for clinicians.Hepatic involvement in hereditary hemorrhagic telangiectasia: CT findings.Neuroradiological Manifestations of Hereditary Hemorrhagic Telangiectasia in 139 Japanese Patients.Sinonasal quality of life outcomes following laser treatment of epistaxis related to hereditary hemorrhagic telangiectasia.Hereditary Haemorrhagic Telangiectasia Cerebrospinal Localization in Adults and Children. Review of 39 cases.
P2860
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P2860
Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Hereditary haemorrhagic telang ...... mortality in Danish patients.
@en
type
label
Hereditary haemorrhagic telang ...... mortality in Danish patients.
@en
prefLabel
Hereditary haemorrhagic telang ...... mortality in Danish patients.
@en
P2093
P2860
P1476
Hereditary haemorrhagic telang ...... mortality in Danish patients.
@en
P2093
P2860
P356
10.1046/J.1365-2796.1999.00398.X
P407
P577
1999-01-01T00:00:00Z