Results 41 to 50 of about 4,853 (149)

Future treatments for hereditary hemorrhagic telangiectasia

Orphanet Journal of Rare Diseases, 2020
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Rendu-Osler syndrome, is a genetic vascular disorder affecting 1 in 5000–8000 individuals worldwide.
Florian Robert, Agnès Desroches-Castan, Sabine Bailly, Sophie Dupuis-Girod, Jean-Jacques Feige   +4 more
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Genetic testing for hereditary hemorrhagic telangiectasia

The EuroBiotech Journal, 2018
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia characterized by telangiectases and arteriovenous malformations. These lesions cause bleeding, particularly in the nose, gastrointestinal tract and brain.
Rakhmanov Yeltay, Maltese Paolo Enrico, Paolacci Stefano, Marinelli Carla, Mattassi Raul Ettore, Amato Bruno, Beccari Tommaso, Dundar Munis, Bertelli Matteo   +8 more
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Benefits of Treating Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Retrospective Analysis of 14 Patients

World Neurosurgery: X, 2019
Background: Arteriovenous malformations (AVMs) are a cardinal feature of hereditary hemorrhagic telangiectasia (HHT). However, whether to treat brain AVMs in patients with HHT remains questionable because of the possible risks.
M. Neil Woodall, Peter Nakaji, Robert F. Spetzler   +2 more
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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
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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
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Laryngeal Hereditary Hemorrhagic Telangiectasia [PDF]

Ear, Nose & Throat Journal, 2018
Jérôme R, Lechien, Camille, Finck
openaire   +2 more sources

Telangiectasia hemorrágica hereditária e malformações arteriovenosas pulmonares - Embolização com rolhão vascular Amplatzer Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations - Embolization with Amplatzer vascular plug

Revista Portuguesa de Pneumologia, 2009
As malformações arteriovenosas pulmonares (MAVP) estão associadas a telangiectasia hemorrágica hereditária em cerca de 70% dos casos, podendo cursar com complicações neurológicas graves decorrentes do embolismo paradoxal potencial.
Cláudia Sofia Santos, Ana Norte, Ilda Ferreira, Paulo Almeida, A Segorbe Luís, Mário Loureiro, M Fontes Baganha   +6 more
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A case report of acute myocardial infarction with hereditary hemorrhagic telangiectasia

Journal of Cardiothoracic Surgery
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by epistaxis, gastrointestinal bleeding, iron deficiency anemia, and arteriovenous malformations (AVMs) affecting the lungs, liver, and brain. Owing to its rarity
Wenping Xue, Wei Qin, Tingting Liu, Weichao Shan   +3 more
doaj   +1 more source

Brain abscess and hereditary hemorrhagic telangiectasia [PDF]

Arquivos de Neuro-Psiquiatria, 2022
Leonardo Furtado FREITAS, Márcio Luís DUARTE, Eduardo Carvalho MIRANDA   +2 more
doaj   +1 more source

Optimal management of hereditary hemorrhagic telangiectasia

Journal of Blood Medicine, 2014
Neetika Garg,1 Monica Khunger,2 Arjun Gupta,3 Nilay Kumar4 1Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA; 2Department of Medicine, All India Institute of Medical Sciences, New Delhi, India; 3Department of Medicine, UT ...
Garg N, Khunger M, Gupta A, Kumar N
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