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International Journal of Clinical Practice|November 25, 2003
Pulmonary arteriovenous malformation: a rare, treatable cause of stroke in young adultsR R Retnakaran, M E Faughnan, R P Chan, et al.Orphanet Journal of Rare Diseases|November 7, 2022
Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasiaK P Thompson, J Sykes, P Chandakkar, et al.Laryngoscope Investigative Otolaryngology|March 2, 2026
Characterizing Self-Reported Daily Diary Epistaxis Measures in Hereditary Hemorrhagic TelangiectasiaC M Tarulli, X Ma, A M Bayoumi, et al.Journal of Medical Genetics|July 5, 2003
Visceral manifestations in hereditary haemorrhagic telangiectasia type 2S A Abdalla, U W Geisthoff, D Bonneau, et al.Orphanet Journal of Rare Diseases|September 20, 2021
Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasiaK P Thompson, J Nelson, H Kim, et al.Chest|January 13, 2000
Diffuse pulmonary arteriovenous malformations: characteristics and prognosisM E Faughnan, Y W Lui, J A Wirth, et al.American Journal of Medical Genetics|April 6, 2000
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)C L Shovlin, A E Guttmacher, E Buscarini, et al.Orphanet Journal of Rare Diseases|April 23, 2016
Life expextancy of parents with Hereditary Haemorrhagic TelangiectasiaE M de Gussem, C P Edwards, A E Hosman, et al.Chest|February 15, 2001
Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancyA S Gershon, M E Faughnan, K S Chon, et al.American Heart Journal|February 15, 2001
Contrast echocardiography for detection of pulmonary arteriovenous malformationsK Nanthakumar, A T Graham, T I Robinson, et al.Pageof 3