Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Rendu osler disease"'
Autor:
Thi Thao Truc Le, Guillaume Martinent, Sophie Dupuis-Girod, Antoine Parrot, Anne Contis, Sophie Riviere, Thierry Chinet, Vincent Grobost, Olivier Espitia, Brigitte Dussardier-Gilbert, Laurent Alric, Guillaume Armengol, Hélène Maillard, Vanessa Leguy-Seguin, Sylvie Leroy, Murielle Rondeau-Lutz, Christian Lavigne, Shirine Mohamed, Laurent Chaussavoine, Pascal Magro, Julie Seguier, Mallorie Kerjouan, Sylvie Fourdrinoy
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) disease is a rare genetic disorder with symptoms and complications that can significantly affect patients’ daily lives. To date, no scale has been validated to assess the specific symp
Externí odkaz:
https://doaj.org/article/cecf83f4ed6f4dbb8475401e0e67d5cb
Akademický článek
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Publikováno v:
Reviews on recent clinical trials. 15(4)
Background: Hereditary hemorrhagic telangiectasia (HHT, or Rendu-Osler-Weber disease) is a rare inherited syndrome, characterized by artero-venous malformations (AVMs or telangiectasia) with autosomal dominant transmission. AVMs can occur in any orga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b2bae39bea43add122651df7a4eb835
https://pubmed.ncbi.nlm.nih.gov/32493201
https://pubmed.ncbi.nlm.nih.gov/32493201
Autor:
G. De Luna, A. Passeron, Jacques Pouchot, A. Michon, V. Bourdin, P. Lozac’h, Jean-Benoît Arlet, J. Lapoirie, Brigitte Ranque
Publikováno v:
La Revue de Médecine Interne. 39:134-137
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7109f17e3bff6249476fabee94b6f81e
https://doi.org/10.1016/j.revmed.2017.06.024
https://doi.org/10.1016/j.revmed.2017.06.024
Publikováno v:
JMV-Journal de Médecine Vasculaire. 44:76-78
Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Venous thromboembolic disease is a poor prognostic factor in this disease g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53c45c13a697b74fc72ceacfcd9ce010
https://doi.org/10.1016/j.jdmv.2018.11.003
https://doi.org/10.1016/j.jdmv.2018.11.003
Publikováno v:
Bulletin physiology and pathology of respiration. 1:91-97
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4defb1c99dff67fec7efe6f3eb5e9bc0
https://doi.org/10.12737/article_58e45dce7e75d0.73462907
https://doi.org/10.12737/article_58e45dce7e75d0.73462907
Publikováno v:
Diagnostic and Interventional Imaging. 97(4):451-459
Purpose To evaluate the agreement between the Buscarini criteria on ultrasound (US) and multiphase contrast-enhanced multidetector-row computed tomography (MDCT) in the diagnosis and staging of liver involvement in hereditary hemorrhagic telangiectas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949a72b22d118de0a49f993723b2954d
Autor:
S. Binsse, I. Bourgault-Villada, C. Fagnou, M. Bensalah, Thierry Chinet, P Y Marcy, G. Lesur, S. Blivet, A Lacout, J. Sellier, Pascal Lacombe, A. Ozanne, J. Roume, J.-H. Blondel, M. El Hajjam, S. Chagnon
Publikováno v:
Diagnostic and Interventional Imaging. 94(9):835-848
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease is an autosomic dominant disorder, which is characterized by the development of multiple arteriovenous malformations in either the skin, mucous membranes, and/or visceral organs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9595ed2fbb184c4bd02e7cafa6665dc
Publikováno v:
Respiration
Respiration, Karger, 2017, 94 (4), pp.315-330. ⟨10.1159/000479632⟩
Respiration, Karger, 2017, 94 (4), pp.315-330. ⟨10.1159/000479632⟩
International audience; Hereditary hemorrhagic telangiectasia (HHT) is a dominantly inherited genetic vascular disorder with an estimated prevalence of 1 in 6,000, characterized by recurrent epistaxis, cutaneous telangiectasia, and arteriovenous malf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ee822b1f7a4b84bafec71158a86fa21
https://hal.inrae.fr/hal-02620517
https://hal.inrae.fr/hal-02620517
Publikováno v:
Revue Neurologique. 167:29-34
Resume Introduction Les malformations arterioveineuses pulmonaire (MAVP), survenant le plus souvent lors d’une maladie de Rendu Osler (HHT), se compliquent dans 5 a 13 % des cas d’un abces cerebral. Observation Un homme âge de 51 ans, cadre supe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d593f433a53e4eb0ff1b48afd15e5543
https://doi.org/10.1016/j.neurol.2010.03.019
https://doi.org/10.1016/j.neurol.2010.03.019