Results 91 to 100 of about 9,783 (206)

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

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects. [PDF]

, 2015
Pulmonary arterial hypertension (PAH) is an often fatal disorder resulting from several causes including heterogeneous genetic defects. While mutations in the bone morphogenetic protein receptor type II (BMPR2) gene are the single most common causal ...
Abdalla, Adzhubei, Aldred, Aldred, Archer, Austin, Austin, Austin, Badesch, Best, Best, Chaouat, Chen, Chida, Chida, Chidlow, Choi, Cogan, Cogan, Dahal, David, Deng, Donnelly, Drab, Drake, Elliott, Eyries, Eyries, Feng, Foletta, Frydman, Fujiwara, Germain, Girerd, Girerd, Girerd, Greenwald, Harrison, Harrison, Hinderhofer, Hong, Huang, Humbert, Ishiwata, Jones, Kabata, Koehler, Kumar, Lane, Larkin, Liu, Liu, Long, Ma, Machado, Machado, Machado, Machado, Mache, Mair, Maniatis, McLaughlin, Mercier, Minshall, Murata, Möller, Nasim, Nasim, Nishihara, Nohe, Pfarr, Pfarr, Ranchoux, Remillard, Rigueur, Rosenzweig, Rudarakanchana, Ryan, Shi, Shintani, Simonneau, Smoot, Sobolewski, Soubrier, Sztrymf, Tenorio, Thomson, Trembath, Tuder, Vonk-Noordegraaf, Wang, Wang, Wang, West, West, West, Xu, Young, Yuan, Zhao, Zhao   +100 more
core   +2 more sources

Incidental pulmonary arteriovenous malformation

Journal of Hospital Medicine, Volume 21, Issue 5, Page 599-600, May 2026.
Mallory A. Von Lotten, Eric Howell, J. Andrew Watson   +2 more
wiley   +1 more source

Cerebral Abscess in a Patient with Rendu-Osler-Weber [PDF]

, 2015
A telangiectasia hemorrágica hereditária é uma doença familiar rara, descrita pela primeira vez no final do século 19, caracterizada por telangiectasias mucocutâneas e viscerais, e por malformações arteriovenosas.
Malhado, JA, Neves, Z, Pacheco, MH, Segura, U, Valente, A   +4 more
core  

Método de detección de la Telangiectasia Hemorrágica Hereditaria [PDF]

, 2008
Método de detección de la Telangiectasia Hemorrágica Hereditaria. Método para la detección de la Telangiectasia Hemorrágica Hereditaria (HHT) que comprende el análisis in vitro de los productos de la expresión de los genes ENG o FLT1 Y ENG o ANGPT2 ...
Barrios, Laura, Bernabéu, Carmelo, Botella, Luisa María, Ojeda-Fernández, María Luisa   +3 more
core  

The TGFβ type I receptor TGFβRI functions as an inhibitor of BMP signaling in cartilage. [PDF]

, 2019
The type I TGFβ receptor TGFβRI (encoded by Tgfbr1) was ablated in cartilage. The resulting Tgfbr1 Col2 mice exhibited lethal chondrodysplasia. Similar defects were not seen in mice lacking the type II TGFβ receptor or SMADs 2 and 3, the intracellular ...
Baek, Jongseung, Chun, Hyelim, Lopez, Noah, Lyons, Karen M, Razavi, Peyman, Sadik, Joshua Elyahu, Shirazyan, Anna, Wang, Weiguang   +7 more
core  

Hereditary Hemorrhagic Telangiectasia - a literature review

Journal of Education, Health and Sport
Introduction and purpose: Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a rare and complex vascular disorder characterized by abnormal blood vessel formation.
Marcel Stodolak, Aleksandra Krużel, Kamil Kłos, Piotr Sajdak, Justyna Tomasik, Marika Dębik, Łukasz Szydłowski, Klaudia Żurowska, Seweryn Ziajor, Artur Bednarski, Mikołaj Turski   +10 more
doaj   +1 more source

Caractéristiques cliniques et parcours médical des patients atteints de la maladie de Rendu-Osler suivis au CHUV [PDF]

, 2014
Objectifs : Les objectifs de ce travail ont consisté à décrire les caractéristiques cliniques et la prise en charge des patients atteints de maladie de Rendu-Osler (MRO) évalués par le réseau multidisciplinaire du CHUV, le parcours médical de ces
FRIGERIO, C.
core  

Un nuevo tratamiento para las epístaxis de la enfermedad de Rendu-Osler-Weber ó telangiectasia hemorrágica hereditaria (HHT). [PDF]

, 2013
Hereditary Haemorrhagic Telangiectasia or Rendu-Osler-Weber syndrome is an autosomal dominant vascular rare disease whose clinical manifestations are mucocutaneous and gastrointestinal telangiectases and localized arteriovenous malformations in lung ...
Morais Pérez, Darío
core   +1 more source

Pericardial Involvement in Hereditary Hemorrhagic Telangiectasia

Acta Medica Iranica
Hereditary haemorrhagic telangiectasia is a rare disease characterized by cutaneo-mucous and visceral arteriovenous malformations. Cardiac involvement is uncommon and was presented primarily by hyper-output heart failure.
Abir Derbel, Mouna Snoussi, Raida Ben Salah, Faten Frikha, Leila Abid, Imed Frikha, Sameh Marzouk, Zouhir Bahloul   +7 more
doaj   +1 more source