Intravenous immunoglobulins for the treatment of prolonged COVID-19 in immunocompromised patients: a brief report

Autor: Bénédicte Billi, Paul Cholley, Vincent Grobost, Mélissa Clément, Virginie Rieu, Guillaume Le Guenno, Hervé Lobbes

Publikováno v: Frontiers in Immunology, Vol 15 (2024)

Primary humoral deficiency and secondary B-cell depletion may lead to prolonged Sars-Cov-2 infection due to a decreased viral clearance. Prolonged infection is mainly driven by the lack of anti-Sars-Cov-2 immunoglobulin (IVIg) especially in patients

Externí odkaz: https://doaj.org/article/51fa62975ab04a07ac518dd8e6e82f9b

Successful treatment of de novo acute myeloid leukaemia associated aortitis by induction chemotherapy alone

Autor: Urbain Tauveron--Jalenques, Vincent Grobost, Benoît Magnin, Cécile Moluçon-Chabrot, Jacques-Olivier Bay, Olivier Tournilhac, Romain Guièze

Publikováno v: Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)

Externí odkaz: https://doaj.org/article/fc028c7b4d844b05ba1a8fd8e4e5ea28

Intracranial pressure monitoring with and without brain tissue oxygen pressure monitoring for severe traumatic brain injury in France (OXY-TC): an open-label, randomised controlled superiority trial

Autor: Fevre, Marie-Cecile, SCHILTE, Clotilde, Vincent, Olivier, Hérault, Marie-Christine, Mistral, Thomas, Trouve-Buisson, Thibaut, Picard, Julien, Falcon, Dominique, Bersinger, Samuel, Mourey, Clément, Adolle, Anaïs, Salah, Samia, Manhes, Pauline, Pollet, Angélina, GRECO, Frédéric, CHALARD, kevin, Andréa, Bailleul, Velly, Lionel, Bruder, Nicolas, Inal, Imane, Magand, Clément, Burnol, Laetitia, Morel, Jérôme, PREGNY, Anaèle, FERRE, Jean-Christophe, Bannier, Elise, Lebouvier, Thomas, Caradec, Sophie, Drevet, Claire-Marie, Nadji, Abdelouaid, Lewandowski, Romain, DAILLER, Frédéric, CARRILLON, Romain, GOBERT, Florent, RITZENTHALER, Thomas, LECLERCQ, Mathilde, Dumont, Nathalie, Charpentier, Claire, Alb, Ionel, De Sa, Natalie, Declerck, Nicolas, Boussemart, Pierre, Bellet, Julie, MEAUDRE-DESGOUTTES, Eric, D'ARANDA, Erwan, ESNAULT, Pierre, CHARRUAU, Camille, BELLIER, Rémy, BENARD, Thierry, Carise, Elsa, SEGUIN, Sabrina, Lefrant, Jean Yves, Daurat, Aurélien, Ambert, Audrey, Lebouc, Marie, Hautefeuille, Serge, Escudier, Etienne, Bing, Fabrice, Cosserant, Bernard, Grobost, Romain, Boissy, Camille, Begard, Marc, Guyot, Adrien, Lagarde, Kevin, Caumon, Elodie, Geeraerts, Thomas, POMMIER, Maxime, NABOULSI, Edouard, BEILVERT, Maxime, PARRY, Elodie, Leone, Marc, Zieleskiewicz, Laurent, Duclos, Gary, Arbelot, Charlotte, Carole, Ichai, Hervé, Quintard, Aminata, Diop, Puybasset, Louis, Torkomian, Gregory, Szczot, Magdalena, Kremer, Stephane, Becker, Guillaume, Hecketsweiler, Stephane, ILIC, Dejan, VETTORETTI, Lucie, Grisotto, Coline, Asmolov, Romain, Ehinger, Vincent, Laquay, Nathalie, Chevallier, Virginie, Mahlal, Zahra, LASOCKI, Sigismond, SCHOLASTIQUE, Anne-Sylvie, GAILLARD, Thomas, GERGAUD, Soizic, BARBIER, Emmanuel, TAHON, Florence, KRAINIK, Alexandre, DOJAT, Michel, TROPRES, Irène, VIGUE, Bernard, LEO, Laura, Piriou, Vincent, Coquerel, Antoine, Cracowski, Jean-Luc, Proust, Francois, Mallaret, Michel, Payen, Jean-François ^*, Launey, Yoann, Chabanne, Russell, Gay, Samuel, Francony, Gilles, Gergele, Laurent, Vega, Emmanuel, Montcriol, Ambroise, Couret, David, Cottenceau, Vincent, Pili-Floury, Sebastien, Gakuba, Clement, Hammad, Emmanuelle, Audibert, Gerard, Pottecher, Julien, Dahyot-Fizelier, Claire, Abdennour, Lamine, Gauss, Tobias, Richard, Marion, Vilotitch, Antoine, Bosson, Jean-Luc, Bouzat, Pierre

Publikováno v: In The Lancet Neurology November 2023 22(11):1005-1014

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Development and validation of a quality of life measurement scale specific to hereditary hemorrhagic telangiectasia: the QoL-HHT

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