Hereditary Hemorrhagic Telangiectasia (HHT) is easily recognized in individuals displaying
the classical triad of epistaxis, telangiectasia, and a suitable family history, but the disease is …

… (b) Illustration of two separate pathologies resulting in severe pulmonary hypertension in
two women with HHT (reported in Shovlin et al 6 ). Note case 1 has markedly elevated intrinsic …

Hereditary haemorrhagic telangiectasia, inherited as an autosomal dominant trait, affects
approximately 1 in 5000 people. The abnormal vascular structures in HHT result from …

Hereditary haemorrhagic telangiectasia (HHT) affects one in 5−8000, and no longer can be
viewed as solely causing anaemia (due to nasal and gastrointestinal bleeding) and …

Hereditary haemorrhagic telangiectasia (HHT, Rendu-Osler-Weber syndrome) exemplifies
an important group of diseases which have catalysed advances in the understanding of …

Patients with hereditary haemorrhagic telangiectasia (HHT, or Osler-Weber-Rendu
syndrome) have variable presentation patterns and a high risk of preventable complications. …

… CL Shovlin1,4, … Dr CL Shovlin, NHLI Cardiovascular Sciences, Imperial College
London, Hammersmith Hospital, Du Cane Road, London W12 0NN, UK; c.shovlin{at}imperial.ac.uk …

INTRODUCTION Need for new recommendations for managing passengers with respiratory
disease planning air travel Since the first British Thoracic Society (BTS) recommendations …

… Roked F, Jackson JE, Fuld J, Basheer FT, Chilvers ER, Beattie S, Shovlin CL. Pulmonary
thromboemboli modifying the natural history of pulmonary arteriovenous malformations. Am J …

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder
that is characterized by frequent nosebleeds, mucocutaneous telangiectases and vascular …