Results 111 to 120 of about 1,710,432 (174)

Rendu-Osler-Weber Syndrome With Big Pulmonary Artero-Venous Malformation (Pavm) And Associated Foramen Ovale Patency (Fop)

, 2019
A 55 years old woman with a personal history of brain abscesses, recurrent epistaxis and transient ischemic attacks, underwent Mininvasive Surgery with atrial septal device positioning.
Francesco Inzirillo, Marialuisa Di Matteo, Claudio Della Pona   +2 more
core   +1 more source

Optimizing the Interventional Approach for Embolization of Pulmonary Arteriovenous Malformations in Patients With Osler-Weber-Rendu Syndrome. [PDF]

Cureus, 2020
McFarland JR, Harmon TS, Hunsaker T, Gill G, Bagherpour AN.   +4 more
europepmc   +1 more source

Maladie de Rendu-Osler. Manifestations cliniques et prise en charge multidisciplinaire [Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): clinical manifestations and multidisciplinary management]

, 2016
Hereditary hemorrhagic telangiectasia (HHT), or Osler- Weber-Rendu syndrome, is a rare genetic disorder with autosomal dominant inheritance, characterized by recurrent epistaxis, mucocutaneous telangiectasia and visceral arteriovenous malformations (AVMs)
Frigerio, C., Fellmanne, F., Qanadli, S.D., Mazzolai, L., Lazor, R., Baud, D., Ikonomidis, C., Aebischer, N., Bonafe, L., Michel, P., Nichita, C.   +10 more
core   +1 more source

Rendu-Osler-weber disease. Case report [PDF]

, 2016
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
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Osler-Weber-Rendu Syndrome: a case report [PDF]

, 2016
El síndrome de Rendu-Osler-Weber (SROW), conocido también como Telangiectasia Hemorrágica Hereditaria (THH), es un desorden vascular infrecuente. Se trata de una alteración vascular displásica multisistémica de carácter autosómico dominante, con diversas
Bustamante, Freyli, Tenreiro Picón, Oscar, Tenreiro, Andrea, Bustamante, Ekaterina   +3 more
core  

Reporte de un caso clínico Sindrome de Rendu – Osler – Weber y Sîndrome Antifosfolipido: (Report of a clinical case Rendu – Osler – Weber Syndrome and Antiphospholipid Syndrome)

Rendu-Osler-Weber syndrome (HHT) is a vascular disorder characterized by the presence of telangiectasias and arteriovenous malformations. It is an autosomal dominant multisystem dysplastic vascular disorder.
Pinto Pineda, Verónica Alejandra, Pinto Pineda, Francisco Rafael, Lalama Gómez, Karolin Paulina   +2 more
core   +1 more source

Rendu-Osler-weber disease. Case report

, 2020
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
core  

Scattered arteriovenous malformations in Osler-Weber-Rendu syndrome [PDF]

Journal of Vascular Surgery, 2012
Nassiri, Naiem, Rachakonda, Aditya, Carroccio, Alfio, Rosen, Robert   +3 more
openaire   +2 more sources

Pulmonary arteriovenous malformation in Osler–Weber–Rendu syndrome [PDF]

European Journal of Cardio-Thoracic Surgery, 2009
Sung-Yuan, Hu, Cheng-Han, Tsai, Yu-Tse, Tsan   +2 more
openaire   +2 more sources

Presentation of a rendu-osler-weber patient to emergency department

, 2008
Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia) is an autosomal dominant familial angiogenesis disorder which presents with the clinical consequences of vascular malformations in mucocutaneous tissues, visceral organs and central ...
Serinken, M, Turkcuer, I, Erdur, B
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