Randomized, double-blind, placebo-controlled, crossover trial of oral doxycycline for epistaxis in hereditary hemorrhagic telangiectasia von Thompson, K. P, Sykes, J, Chandakkar, P, Marambaud, P, Vozoris, N. T, Marchuk, D. A, Faughnan, M. E

Volltext

The pulmonary vascular complications of hereditary haemorrhagic telangiectasia von Faughnan, M. E, Granton, J. T, Young, L. H

Volltext

Improved Survival After Liver Transplantation in Patients with Hepatopulmonary Syndrome von Gupta, S., Castel, H., Rao, R. V., Picard, M., Lilly, L., Faughnan, M. E., Pomier‐Layrargues, G.

Volltext

Neurovascular manifestations in hereditary hemorrhagic telangiectasia: imaging features and genotype-phenotype correlations von Krings, T, Kim, H, Power, S, Nelson, J, Faughnan, M E, Young, W L, terBrugge, K G

Volltext

Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia von Thompson, K P, Nelson, J, Kim, H, Weinsheimer, S M, Marchuk, D A, Lawton, M T, Krings, T, Faughnan, M E

Volltext

Idiopathic pulmonary arteriovenous malformations: clinical and imaging characteristics von WONG, H. H, CHAN, R. P, KLATT, R, FAUGHNAN, M. E

Volltext

Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia von Al-Saleh, S, Mei-Zahav, M, Faughnan, M. E, MacLusky, I. B, Carpenter, S, Letarte, M, Ratjen, F

Volltext

International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia von Faughnan, M E, Palda, V A, Garcia-Tsao, G, Geisthoff, U W, McDonald, J, Proctor, D D, Spears, J, Brown, D H, Buscarini, E, Chesnutt, M S, Cottin, V, Ganguly, A, Gossage, J R, Guttmacher, A E, Hyland, R H, Kennedy, S J, Korzenik, J, Mager, J J, Ozanne, A P, Piccirillo, J F, Picus, D, Plauchu, H, Porteous, M E M, Pyeritz, R E, Ross, D A, Sabba, C, Swanson, K, Terry, P, Wallace, M C, Westermann, C J J, White, R I, Young, L H, Zarrabeitia, R

Volltext

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2 von Abdalla, S A, Geisthoff, U W, Bonneau, D, Plauchu, H, McDonald, J, Kennedy, S, Faughnan, M E, Letarte, M

Volltext

Life expectancy of parents with Hereditary Haemorrhagic Telangiectasia von de Gussem, E. M, Edwards, C. P, Hosman, A. E, Westermann, C. J. J, Snijder, R. J, Faughnan, M. E, Mager, J. J

Volltext

SMAD4 gene mutation increases the risk of aortic dilation in patients with hereditary haemorrhagic telangiectasia von Vorselaars, V.M.M., Diederik, A., Prabhudesai, V., Velthuis, S., Vos, J.-A., Snijder, R.J., Westermann, C.J.J., Mulder, B.J., Ploos van Amstel, J.K., Mager, J.J., Faughnan, M.E., Post, M.C.

Volltext

Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia von Matsubara, Shunji, Manzia, Jennifer L, ter Brugge, Karel, Willinsky, Robert A, Montanera, Walter, Faughnan, Marie E

Volltext

Life expextancy of parents with Hereditary Haemorrhagic Telangiectasia von de Gussem, E M, Edwards, C P, Hosman, A E, Westermann, C J J, Snijder, R J, Faughnan, M E, Mager, J J

Volltext

Diffuse pulmonary arteriovenous malformations : Characteristics and prognosis von FAUGHNAN, M. E, LUI, Y. W, WIRTH, J. A, PUGASH, R. A, REDELMEIER, D. A, HYLAND, R. H, WHITE, R. I

Volltext

Contrast echocardiography for detection of pulmonary arteriovenous malformations von Nanthakumar, K., Graham, A.T., Robinson, T.I., Grande, P., Pugash, R.A., Clarke, J.A., Hutchison, S.J., Mandzia, J.L., Hyland, R.H., Faughnan, M.E.

Volltext

Prognostic relevance of dynamic hyperinflation during cardiopulmonary exercise testing in adult patients with cystic fibrosis von Stevens, D, Stephenson, A, Faughnan, M.E, Leek, E, Tullis, E

Volltext

Endoglin-deficient Mice, a Unique Model to Study Hereditary Hemorrhagic Telangiectasia von Bourdeau, Annie, Faughnan, Marie E, Letarte, Michelle

Volltext

PULMONARY ARTERIOVENOUS MALFORMATION: A RARE, TREATABLE CAUSE OF STROKE IN YOUNG ADULTS von Retnakaran, RR, Faughnan, ME, Chan, RP, Pugash, RA, O'Connor, PW, Chow, C‐M

Volltext

Spinal cord arteriovenous malformations in two patients with hereditary hemorrhagic telangiectasia von MANDZIA, J. L, TERBRUGGE, K. G, FAUGHNAN, M. E, HYLAND, R. H

Volltext

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) von Shovlin, Claire L., Guttmacher, Alan E., Buscarini, Elisabetta, Faughnan, Marie E., Hyland, Robert H., Westermann, Cornelius J.J., Kjeldsen, Anette D., Plauchu, Henri

Volltext