Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Pascal Lacombe"'
Autor:
Jacques Sellier, Carma Karam, Alain Beauchet, Axel Dallongeville, Stephen Binsse, Sandra Blivet, Isabelle Bourgault-Villada, Philippe Charron, Thierry Chinet, Mélanie Eyries, Carole Fagnou, Jérome Lesniak, Gilles Lesur, Jérome Lucas, Agnès Nicod-Tran, Augustin Ozanne, Aurélien Palmyre, Florent Soubrier, Mostafa El Hajjam, Pascal Lacombe
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0226681 (2020)
BACKGROUND:Splenic artery aneurysm (SAA) is a rare but potentially fatal condition. Rupture results in 25% mortality up to 75% in pregnant women with 95% fetal mortality. Brief reports suggest an increased risk of developing SAA in patients with HHT.
Externí odkaz:
https://doaj.org/article/5b17dd447d8143a092231c0c98dad292
Autor:
Cécile Rotenberg, Marcel Bonay, Mostafa El Hajjam, Sandra Blivet, Alain Beauchet, Pascal Lacombe, Thierry Chinet
Publikováno v:
BMC Pulmonary Medicine, Vol 17, Iss 1, Pp 1-4 (2017)
Abstract Background Pulmonary arteriovenous malformations (PAVMs) are present in approximately 15–50% individuals with hereditary hemorrhagic telangiectasia (HHT). They may be isolated but more often are multiple. The goal of this study was to eval
Externí odkaz:
https://doaj.org/article/4078645d5a2946b691029e451aa7f8b6
Autor:
Sabine Revuz, Evelyne Decullier, Isabelle Ginon, Nicolas Lamblin, Pierre-Yves Hatron, Pierre Kaminsky, Marie-France Carette, Pascal Lacombe, Anne-Claire Simon, Sophie Rivière, Jean-Robert Harlé, Alain Fraisse, Christian Lavigne, Vanessa Leguy-Seguin, Ari Chaouat, Chahera Khouatra, Sophie Dupuis-Girod, Eric Hachulla
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0184227 (2017)
Different pulmonary hypertension (PH) mechanisms are associated with hereditary haemorrhagic telangiectasia (HHT).We conducted a retrospective study of all suspected cases of PH (echocardiographically estimated systolic pulmonary artery pressure [sPA
Externí odkaz:
https://doaj.org/article/9fbe1814329f4108896a85e2d1ca701b
Publikováno v:
Diagnostic and Interventional Radiology, Vol 19, Iss 1, Pp 70-72 (2013)
A central venous catheter tip located too high into the superior vena cava (SVC) is known to be a strong risk factor for central venous thrombosis and subsequent SVC syndrome. We report herein the usefulness of catheterizing the implanted port cathet
Externí odkaz:
https://doaj.org/article/6c5e1bbaf08e40f49781a12e469e34f1
Autor:
Sandra Blivet, Daniel Cobarzan, Alain Beauchet, Mostafa El Hajjam, Pascal Lacombe, Thierry Chinet
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90937 (2014)
Fifteen to fifty percent of patients with hereditary haemorrhagic telangiectasia have pulmonary arteriovenous malformations. The objective of this study was to measure the effect of the presence of pulmonary arteriovenous malformations and of their e
Externí odkaz:
https://doaj.org/article/52cf1e8a0ee74c7d9980428cd663d9f1
Autor:
Mostafa El Hajjam, Florent Soubrier, Augustin Ozanne, Gilles Lesur, Alain Beauchet, Philippe Charron, Pascal Lacombe, Aurélien Palmyre, Isabelle Bourgault-Villada, Jerome Lucas, Jérome Lesniak, Axel Dallongeville, Carole Fagnou, J. Sellier, Carma Karam, S. Binsse, Thierry Chinet, Mélanie Eyries, Sandra Blivet, Agnès Nicod-Tran
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2020, 15 (1), pp.e0226681. ⟨10.1371/journal.pone.0226681⟩
PLoS ONE, Vol 15, Iss 1, p e0226681 (2020)
PLoS ONE, Public Library of Science, 2020, 15 (1), pp.e0226681. ⟨10.1371/journal.pone.0226681⟩
PLoS ONE, Vol 15, Iss 1, p e0226681 (2020)
International audience; Background: Splenic artery aneurysm (SAA) is a rare but potentially fatal condition. Rupture results in 25% mortality up to 75% in pregnant women with 95% fetal mortality. Brief reports suggest an increased risk of developing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5adef5cc0995e9e23cbbe4f6e33efdb
https://hal.sorbonne-universite.fr/hal-02945460/file/journal.pone.0226681.pdf
https://hal.sorbonne-universite.fr/hal-02945460/file/journal.pone.0226681.pdf
Autor:
Pascal Lacombe
Le tourisme chamanique est un phénomène relativement nouveau en Amazonie. L'intérêt s'est focalisé sur un cocktail de plantes nommé ayahuasca, si bien que l'on peut parler aujourd'hui d'un certain « ayahuasca business ». Si certaines informat
Autor:
Urban W. Geisthoff, Helen M. Arthur, Pascal Lacombe, Whitney Wooderchak-Donahue, Beth L. Roman, Scott O. Trerotola, Sebastiaan Velthuis, Christopher C.W. Hughes, Mary E. Meek, James R. Gossage, Paul Oh
Publikováno v:
Angiogenesis. 18:511-524
Hereditary hemorrhagic telangiectasia (HHT) is a hereditary condition that results in vascular malfor- mations throughout the body, which have a proclivity to rupture and bleed. HHT has a worldwide incidence of about 1:5000 and approximately 80 % of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64da1037f6d438c43b7b4a1817debe29
https://doi.org/10.1007/s10456-015-9482-5
https://doi.org/10.1007/s10456-015-9482-5
Autor:
Pierre Yves Marcy, Pascal Lacombe, Mostafa El Hajjam, Alexis Lacout, Mohamed Karji-Al Marzouqi
Publikováno v:
Polish Journal of Radiology
Summary Background Although being classically located inside the liver parenchyma, hemangiomas may occasionally develop outside the extra-hepatic capsule, thus appearing as a pedunculated mass. Case Report We report the case of a 66-year-old anal can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e62156f1e1f842aa7cd9864790eb81b
http://europepmc.org/articles/PMC4763809
http://europepmc.org/articles/PMC4763809
Autor:
Philippe Charron, Stéphanie Staraci, Mélanie Eyries, Pascal Lacombe, Philippe Dufour, Florent Soubrier, Marie-Victoire Senat, Augustin Ozanne, Thierry Chinet, Aurélien Palmyre
Publikováno v:
Prenatal diagnosis. 37(12)
RASA1-related disease is a rare autosomal dominant disease characterized by capillary malformations, arteriovenous malformations (AVMs), and/or arteriovenous fistulas (AFVs). Penetrance is nearly complete and vascular malformations may cause serious
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b892b25e711989ee856e2ceadeb89f2
https://pubmed.ncbi.nlm.nih.gov/29025196
https://pubmed.ncbi.nlm.nih.gov/29025196