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Frontiers in Genetics|April 28, 2015
Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasiaClaire L ShovlinIntractable & Rare Diseases Research|October 25, 2014
Iron deficiency, ischaemic strokes, and right-to-left shunts: From pulmonary arteriovenous malformations to patent foramen ovale?Claire L ShovlinBlood Reviews|September 28, 2010
Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatmentClaire L ShovlinAmerican Journal of Respiratory and Critical Care Medicine|November 25, 2014
Pulmonary arteriovenous malformationsClaire L ShovlinEjhaem|August 21, 2023
Unsupervised machine learning algorithms identify expected haemorrhage relationships but define unexplained coagulation profiles mapping to thrombotic phenotypes in hereditary haemorrhagic telangiectasiaGhazel Mukhtar, Claire L ShovlinThe Laryngoscope|January 25, 2014
Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasiaAmy Elphick, Claire L ShovlinThorax|September 29, 2011
Flight-related complications are infrequent in patients with hereditary haemorrhagic telangiectasia/pulmonary arteriovenous malformations, despite low oxygen saturations and anaemiaChristopher G Mason, Claire L ShovlinEuropean Journal of Human Genetics : EJHG|April 2, 2009
Hereditary haemorrhagic telangiectasia: a clinical and scientific reviewFatima S Govani, Claire L ShovlinJournal of Angiogenesis Research|August 13, 2010
Fine mapping of the hereditary haemorrhagic telangiectasia (HHT)3 locus on chromosome 5 excludes VE-Cadherin-2, Sprouty4 and other interval genesFatima S Govani, Claire L ShovlinERJ Open Research|April 20, 2017
Pulmonary arteriovenous malformations: evidence of physician under-educationClaire L Shovlin, James R GossagePageof 7