The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care

Hereditary haemorrhagic telangiectasia and pregnancy: a review of the literature

(2020) Olivier Dupuis et al.   Orphanet Journal of Rare Diseases

Autopsy Findings and Venous Thromboembolism in Patients With COVID-19

(2020) Dominic Wichmann et al.   ANNALS OF INTERNAL MEDICINE

Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline

(2020) Jessica M Clarke et al.   JOURNAL OF MEDICAL GENETICS

Hereditary hemorrhagic telangiectasia and liver involvement

(2020) Christine Silvain et al.   Clinics and Research in Hepatology and Gastroenterology

Mutational and phenotypic characterisation of hereditary hemorrhagic telangiectasia

(2020) Claire Shovlin et al.   BLOOD

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

(2020) Omer F. Eker et al.   Orphanet Journal of Rare Diseases

Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia

(2020) Marie E. Faughnan et al.   ANNALS OF INTERNAL MEDICINE

Increase in COVID-19 inpatient survival following detection of Thromboembolic and Cytokine storm risk from the point of admission to hospital by a near real time Traffic-light System (TraCe-Tic)

(2020) Marcela P. Vizcaychipi et al.   Brazilian Journal of Infectious Diseases

Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia

(2019) Elisabetta Buscarini et al.   Orphanet Journal of Rare Diseases

Prevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination

(2019) Claire Shovlin et al.   HAEMATOLOGICA

Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia

(2019) C. L. Shovlin et al.   Orphanet Journal of Rare Diseases

Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1

(2019) Daniel A. Snellings et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Tissue-specific mosaicism in hereditary hemorrhagic telangiectasia: Implications for genetic testing in families

(2018) Jamie McDonald et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT)

(2018) Claire L. Shovlin et al.   Orphanet Journal of Rare Diseases

Pulmonary Hypertension in a Large Cohort with Hereditary Hemorrhagic Telangiectasia

(2017) Veronique Vorselaars et al.   RESPIRATION

The Lung in Hereditary Hemorrhagic Telangiectasia

(2017) Sophie Dupuis-Girod et al.   RESPIRATION

British Thoracic Society Clinical Statement on Pulmonary Arteriovenous Malformations

(2017) Claire L Shovlin et al.   THORAX

ENG mutational mosaicism in a family with hereditary hemorrhagic telangiectasia

(2017) Pernille M. Tørring et al.   Molecular Genetics & Genomic Medicine

Pulmonary hypertension subtypes associated with hereditary haemorrhagic telangiectasia: Haemodynamic profiles and survival probability

(2017) Sabine Revuz et al.   PLoS One

Intravenous amoxicillin/clavulanate for the prevention of bacteraemia following dental procedures: a randomized clinical trial

(2016) J. Limeres Posse et al.   JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY

EASL Clinical Practice Guidelines: Vascular diseases of the liver

(2016)   JOURNAL OF HEPATOLOGY

2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

(2015) Nazzareno Galiè et al.   EUROPEAN HEART JOURNAL

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): a multicentre, non-blinded, randomised trial

(2013) J P Mohr et al.   LANCET

Antiplatelet and Anticoagulant Agents in Hereditary Hemorrhagic Telangiectasia

(2013) Hannah L. Devlin et al.   NEW ENGLAND JOURNAL OF MEDICINE

Hemorrhage-Adjusted Iron Requirements, Hematinics and Hepcidin Define Hereditary Hemorrhagic Telangiectasia as a Model of Hemorrhagic Iron Deficiency

(2013) Helen Finnamore et al.   PLoS One

Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment

(2010) Claire L. Shovlin   BLOOD REVIEWS

International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia

(2009) M. E. Faughnan et al.   JOURNAL OF MEDICAL GENETICS

Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services

(2008) CL Shovlin et al.   BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY