Zobrazeno 1 - 10
of 72
pro vyhledávání: '"François, Hemery"'
Autor:
Nicolas Hoertel, Marina Sánchez-Rico, Pedro de la Muela, Miriam Abellán, Carlos Blanco, Marion Leboyer, Céline Cougoule, Erich Gulbins, Johannes Kornhuber, Alexander Carpinteiro, Katrin Anne Becker, Raphaël Vernet, Nathanaël Beeker, Antoine Neuraz, Jesús M. Alvarado, Juan José Herrera-Morueco, Guillaume Airagnes, Cédric Lemogne, Frédéric Limosin, Pierre-Yves Ancel, Alain Bauchet, Vincent Benoit, Mélodie Bernaux, Ali Bellamine, Romain Bey, Aurélie Bourmaud, Stéphane Breant, Anita Burgun, Fabrice Carrat, Charlotte Caucheteux, Julien Champ, Sylvie Cormont, Christel Daniel, Julien Dubiel, Catherine Ducloas, Loic Esteve, Marie Frank, Nicolas Garcelon, Alexandre Gramfort, Nicolas Griffon, Olivier Grisel, Martin Guilbaud, Claire Hassen-Khodja, François Hemery, Martin Hilka, Anne Sophie Jannot, Jerome Lambert, Richard Layese, Judith Leblanc, Léo Lebouter, Guillaume Lemaitre, Damien Leprovost, Ivan Lerner, Kankoe Levi Sallah, Aurélien Maire, Marie-France Mamzer, Patricia Martel, Arthur Mensch, Thomas Moreau, Nina Orlova, Nicolas Paris, Bastien Rance, Hélène Ravera, Antoine Rozes, Elisa Salamanca, Arnaud Sandrin, Patricia Serre, Xavier Tannier, Jean-Marc Treluyer, Damien Van Gysel, Gaël Varoquaux, Jill Jen Vie, Maxime Wack, Perceval Wajsburt, Demian Wassermann, Eric Zapletal
Publikováno v:
Biological Psychiatry Global Open Science, Vol 3, Iss 1, Pp 56-67 (2023)
Background: Prior research suggests that psychiatric disorders could be linked to increased mortality among patients with COVID-19. However, whether all or specific psychiatric disorders are intrinsic risk factors of death in COVID-19 or whether thes
Externí odkaz:
https://doaj.org/article/91c0cf29a97c4fe2ab8d6067311b61cd
Autor:
Quentin de Roux, Marie Renaudier, Wulfran Bougouin, Johanna Boccara, Vincent Fihman, Raphaël Lepeule, Chamsedine Cherait, Antonio Fiore, François Hemery, Jean-Winoc Decousser, Olivier Langeron, Nicolas Mongardon
Publikováno v:
Critical Care, Vol 25, Iss 1, Pp 1-11 (2021)
Abstract Background Bloodstream infections (BSIs) are frequent on veno-arterial extracorporeal membrane oxygenation (V-A ECMO). Performing routine blood cultures (BCs) may identify early paucisymptomatic BSIs. We investigated the contribution of syst
Externí odkaz:
https://doaj.org/article/7133c920d7f1457596971716d33e24d8
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-5 (2021)
Abstract Neurofibromatosis 1 (NF1) is an inherited, autosomal-dominant, tumor predisposition syndrome with a birth incidence as high as 1:2000. A patient with NF1 is four to five times more likely to develop a malignancy as compared to the general po
Externí odkaz:
https://doaj.org/article/af92d7c4cd8842b0a1f8c5f2a9d90b0a
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-4 (2020)
Abstract Neurofibromatosis 1 (NF1) is one of the most common autosomal dominant genetic disorders with a birth incidence as high as 1:2000. It is caused by mutations in the NF1 gene on chromosome 17 which encodes neurofibromin, a regulator of neurona
Externí odkaz:
https://doaj.org/article/0383e77cd42241fc86c9240c6873a748
Autor:
David Calvet, Titien Tuilier, Nicolas Mélé, Guillaume Turc, Anoosha Habibi, Nassim Ait Abdallah, Loubna Majhadi, François Hemery, Myriam Edjlali, Frédéric Galacteros, Pablo Bartolucci
Publikováno v:
Blood Advances, Vol 1, Iss 26, Pp 2503-2509 (2017)
Abstract: Silent white matter changes (WMCs) on brain imaging are common in individuals with sickle cell disease (SCD) and are associated with cognitive deficits in children. We investigated the factors predictive of WMCs in adults with homozygous SC
Externí odkaz:
https://doaj.org/article/8562bf264c2445e3b3ab47cbaf5c3cef
Autor:
Baptiste Pignon, Cynthia Borel, Mohamed Lajnef, Jean-Romain Richard, Andrei Szöke, François Hemery, Marion Leboyer, Gilles Foret, Franck Schürhoff
Publikováno v:
Environmental Science and Pollution Research. 29:88577-88586
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::310e97ee286d33a39e7d93940ea54b6b
https://doi.org/10.1007/s11356-022-21964-7
https://doi.org/10.1007/s11356-022-21964-7
Autor:
Emmanuelle Diaz, Christina Bergqvist, Bastien Peiffer, Laura Fertitta, Arnaud Jannic, Salah Ferkal, Ouidad Zehou, François Hemery, Emilie Sbidian, Pierre Wolkenstein
Publikováno v:
Journal of Investigative Dermatology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::536bddb0636d53c8a9ef73ab4f3789b4
https://doi.org/10.1016/j.jid.2023.04.034
https://doi.org/10.1016/j.jid.2023.04.034
Autor:
Nathalie Ganne, François Hemery, Laurent Quero, Frédéric Prat, Thomas Aparicio, Nicola de Angelis, Gilles Galula, Richard Layese, Marc-Antoine Benderra, Atanas Pachev, Christophe Tournigand, Elena Paillaud, Florence Canouï-Poitrine
Publikováno v:
Digestive and Liver Disease
Digestive and Liver Disease, WB Saunders, 2021, ⟨10.1016/j.dld.2021.09.017⟩
Digestive and Liver Disease, Elsevier, 2021, ⟨10.1016/j.dld.2021.09.017⟩
Digestive and Liver Disease, WB Saunders, 2021, ⟨10.1016/j.dld.2021.09.017⟩
Digestive and Liver Disease, Elsevier, 2021, ⟨10.1016/j.dld.2021.09.017⟩
International audience; Background: The coronavirus disease 2019 (COVID-19) pandemic has had a dramatic impact on cancer diagnosis and treatment. Most patients newly diagnosed with digestive system cancer are aged 65 and over. Methods: We performed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95090c68d4e47428b24066347f2ecd7f
https://doi.org/10.1016/j.dld.2021.09.017
https://doi.org/10.1016/j.dld.2021.09.017
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-5 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Neurofibromatosis 1 (NF1) is an inherited, autosomal-dominant, tumor predisposition syndrome with a birth incidence as high as 1:2000. A patient with NF1 is four to five times more likely to develop a malignancy as compared to the general population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a7fedf62d3dce674a48ac2ace2c5b2
https://doaj.org/article/af92d7c4cd8842b0a1f8c5f2a9d90b0a
https://doaj.org/article/af92d7c4cd8842b0a1f8c5f2a9d90b0a
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-4 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Neurofibromatosis 1 (NF1) is one of the most common autosomal dominant genetic disorders with a birth incidence as high as 1:2000. It is caused by mutations in the NF1 gene on chromosome 17 which encodes neurofibromin, a regulator of neuronal differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bf918dca1bf1cfa9dcebb62d7597094
http://link.springer.com/article/10.1186/s13023-020-01463-z
http://link.springer.com/article/10.1186/s13023-020-01463-z