Results 31 to 40 of about 3,300 (212)

Quality of life in patients with hereditary haemorrhagic telangiectasia (HHT) [PDF]

, 2017
Background: There are very few studies about general quality of life parameters, standards for the description of health status and comparison with general population data on patients with Hereditary hemorrhagic telangiectasia (HHT), a rare disease in ...
AD Kjeldsen, Ana Fontalba, AO Geirdal, AØ Geirdal, Blanca Señaris, CA Merlo, CL Shovlin, Concepción Fariñas-Álvarez, D Slotosch, EM Gussem De, EuroQol group, FS Govani, G Pasculli, GA Latino, GD Azevedo, I Gaminde, I Ingrand, JB Hoag, José Antonio Parra, L Bruschini, Luisa María Botella, M Pfister, M Rué, M Serra, ME Faughnan, Miguel Santibáñez, OS Aassar, Roberto Zarrabeitia, S Caruso, S Dheyauldeen, UW Geisthoff, V Albiñana, X Badía   +32 more
core   +3 more sources

Pulmonary arteriovenous malformation

Journal of the Belgian Society of Radiology, 2011
A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
E Janssens, P Leyman, T De Beule, L Ardies, P D’haenens   +4 more
doaj   +1 more source

Endovascular treatment of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia. [PDF]

, 2015
PRINCIPLES: To assess the efficiency and complication rates of vaso-occlusion of pulmonary arteriovenous malformations (PAVMs) in Rendu-Osler-Weber disease (hereditary haemorrhagic telangectasia; HHT).
Aebischer, N., Babaker, M., Beigelman, C., Breault, S., Lazor, R., Qanadli, S.D.   +5 more
core   +1 more source

[Rendu-Osler-Weber disease]. [PDF]

Nederlands tijdschrift voor tandheelkunde, 2005
Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT) is a multisystem autosomal dominant hereditary disorder. The disorder is manifested by multiple dysplasia of blood vessels of the skin and mucous membranes. This results in recurrent and sometimes severe bleeding, of which epistaxis is the most common.
Sys, L.M., Hoogen, F.J.A. van den
openaire   +2 more sources

Massive Hemothorax by Ruptured Arteriovenous Malformation [PDF]

Modern Medicine
Introduction and objectives: Osler Weber Rendu disease is a rare genetic disorder characterized by multiple telangiectasias and arteriovenous malformations involving parenchymatous organs, leading to hemorrhagic, sometimes life threatening vascular ...
Genoveva CADAR, Otilia RADU
doaj   +1 more source

Dietary supplement use and nosebleeds in hereditary haemorrhagic telangiectasia - an observational study. [PDF]

, 2016
Understanding potential provocations of haemorrhage is important in a range of clinical settings, and particularly for people with abnormal vasculature.
Chamali, B, Finnamore, H, Hickson, M, Laffan, MA, Manning, R, Shovlin, CL, Whelan, K   +6 more
core   +2 more sources

Ischaemic strokes in patients with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia: associations with iron deficiency and platelets. [PDF]

, 2014
BackgroundPulmonary first pass filtration of particles marginally exceeding ∼7 µm (the size of a red blood cell) is used routinely in diagnostics, and allows cellular aggregates forming or entering the circulation in the preceding cardiac cycle to lodge ...
AD Kjeldsen, AD Kjeldsen, AE Guttmacher, AJ Easey, B Barzilai, B Nieswandt, Basel Chamali, BD Butler, BJ Folz, BM Silva, C Coupland, C Shovlin, CJ Gallione, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, Claire L. Shovlin, DW Johnson, E Buscarini, ER Chilvers, ER Weibel, F Roked, Gillian Angus, H Finnamore, Hannah C. Tighe, HL Devlin, IS Anand, J Feinstein, J Parra, J Remy, JA Dutton, JA Feinstein, JA Livesey, James E. Jackson, JE Van de Pette, JJ Mager, JL Hart, John A. Livesey, John Meek, K Clark, K Hara, K Nanthakumar, K Ono, K Zukotynski, KL Furie, Klaus Brusgaard, LC Weng, LS Valberg, M Bajc, M Billinger, M Blomley, M Moussouttas, M Nakayama, M Yeung, ME Faughnan, Michael A. Laffan, MK Whyte, MW van Gent, MW van Gent, OS AAssar, P Gazzaniga, P Gupta, P Shovlin CL, Wilmshurst, PC Hébert, RD Thompson, RF Gillum, Richard Manning, S Jackson, S Uchiyama, S Velthuis, SM Bang, T Krings, T Ueki, V Cottin, Vatshalan Santhirapala, WB Porter, Y Benjamini, Y Shinohara, Z Hao   +83 more
core   +4 more sources

Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case

European Journal of Case Reports in Internal Medicine, 2020
Rendu-Osler-Weber syndrome is a rare inherited syndrome with autosomal dominant transmission characterized by systemic arteriovenous malformations (AVMs) with multi-organ involvement.
Maria Inês Silva, Clara Matos, Fabio Correia, Sofia Carola, Maria João Gomes, Teresa Branco   +5 more
doaj   +1 more source

Hereditary Hemorrhagic Telangiectasia

Pediatric Neurology Briefs, 1998
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu disease, was the subject of an NIH workshop, organized by the National Heart, Lung, and Blood Institute, on July 10-11, 1997.
J Gordon Millichap
doaj   +1 more source

Mice Lacking Endoglin in Macrophages Show an Impaired Immune Response [PDF]

, 2016
Endoglin is an auxiliary receptor for members of the TGF-β superfamily and plays an important role in the homeostasis of the vessel wall. Mutations in endoglin gene (ENG) or in the closely related TGF-β receptor type I ACVRL1/ALK1 are responsible for a ...
Aristorena, M., Arthur, H.M., Bernabeu, C., Blanco, F.J., Botella, L.M., Corbí, Á., De las Casas-Engel, M., Gallardo-Vara, E., Lastres, P., Ojeda-Fernández, L., Recio-Poveda, L., Sanz-Rodríguez, F.   +11 more
core   +2 more sources