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Progress in Pediatric Cardiology
Volume 22, Issue 2
, Pages 175-177
, September 2006
Hereditary hemorrhagic teleangectasia: Interventional treatment of pulmonary arteriovenous malformations in the pediatric population
References
- . Hereditary haemorrhagic teleangectasia (Osler-Weber-Rendu syndrome): a view from the 21st century. Postgrad Med J. 2003;79:18–24
- . Genetic abnormalities in hereditary hemorrhagic teleangectasia. Curr Opin Hematol. 1998;5:332–335
- . A hereditary haemorrhagic teleangectasia family with pulmonary involvement is unlinked to the known hereditary hemorrhagic teleangectasia genes, endogline and ALK-1. Thorax. 2000;55:685–690
- Hereditary hemorrhagic teleangectasia with extensive liver involvement is not caused by either HHT1 or HHT2. J Med Genet. 1996;33:441–443
- . Hereditary hemorrhagic teleangectasia: what the otolaryngologist should know. Am J Rhinol. 1997;11:55–62
- . Gastrointestinal lesions in hereditary hemorrhagic teleangectasia. Gastroenterology. 1986;91:1079–1082
- . Pulmonary arteriovenous malformations. Screening procedures and pulmonary angiography in patients with hereditary hemorrhagic teleangectasia. Chest. 1999;116:432–439
- Diagnostic criteria for hereditary hemorrhagic teleangectasia (Rendu-Osler-Weber syndrome). Is J Med Genet. 2000;91:66–67
- . Pulmonary arteriovenous malformations: diagnosis and transcatheter embolotherapy. J Vasc Interv Radiol. 1996;7:787–804
PII: S1058-9813(06)00050-6
doi: 10.1016/j.ppedcard.2006.07.006
© 2006 Elsevier Ireland Ltd. All rights reserved.
« Previous
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Progress in Pediatric Cardiology
Volume 22, Issue 2
, Pages 175-177
, September 2006
