Rare diseases bullet 4: Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms
- 1 August 1999
- Vol. 54 (8), 714-729
- https://doi.org/10.1136/thx.54.8.714
Abstract
No abstract availableKeywords
This publication has 94 references indexed in Scilit:
- Cloning and Characterization of the Murine Activin Receptor-like Kinase-1 (ALK-1) HomologBiochemical and Biophysical Research Communications, 1995
- Liver transplantation for hepatic arteriovenous malformation in hereditary haemorrhagic telangiectasiaJournal of Hepatology, 1995
- Modulation of vascular cell behavior by transforming growth factors ?Molecular Reproduction and Development, 1992
- Antibiotic prophylaxis for patients with hereditary hemorrhagic telangiectasiaJournal of the American Academy of Dermatology, 1992
- Two-dimensional contrast echocardiography in the detection and follow-up of congenital pulmonary arteriovenous malformationsThe American Journal of Cardiology, 1991
- Embolic abscesses in hereditary hemorrhagic telangiectasiaJournal of the American Academy of Dermatology, 1991
- Rendu-Osler-Weber disease with portosystemic encephalopathy.Japanese Journal of Medicine, 1987
- Multiple microscopic pulmonary arteriovenous connections in the lungs presenting as cyanosis.Thorax, 1985
- Pitfall in the CT Diagnosis of Pulmonary Arteriovenous MalformationJournal of Computer Assisted Tomography, 1983
- Pulmonary Arteriovenous MalformationsNew England Journal of Medicine, 1983