Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Isabelle Halphen"'
Autor:
Isabelle Halphen, Caroline Elie, Valentine Brousse, Muriel Le Bourgeois, Slimane Allali, Damien Bonnet, Mariane de Montalembert
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e97462 (2014)
Hypoxia is a common feature in children with sickle cell disease (SCD) that is inconsistently associated with painful crises and acute chest syndrome. To assess the prevalence and risk factors of hypoxia, we recorded daytime, nocturnal, and postexerc
Externí odkaz:
https://doaj.org/article/5bbe02f8289a4d898f54ab106dfe3eb6
Autor:
Alice Hadchouel, Fabrice Decobert, Marie-Laure Franco-Montoya, Isabelle Halphen, Pierre-Henri Jarreau, Olivier Boucherat, Emmanuel Martin, Alexandra Benachi, Serge Amselem, Jacques Bourbon, Claude Danan, Christophe Delacourt
Publikováno v:
PLoS ONE, Vol 3, Iss 9, p e3188 (2008)
BACKGROUND: Alveolarization requires coordinated extracellular matrix remodeling, a process in which matrix metalloproteinases (MMPs) play an important role. We postulated that polymorphisms in MMP genes might affect MMP function in preterm lungs and
Externí odkaz:
https://doaj.org/article/70d898cdc658491c95185449996137bf
Autor:
Claire Demongeot, Manuelle Viguier, Jean-Jacques Boffa, Stéphanie Tellier, Margarita Hurtado-Nedelec, Vincent Pestre, Gérard Cheron, Guillaume Burda, Martin Flamant, Héloïse Flament, Jérôme Verine, Alexandre Seidowsky, E Bourrat, Stéphane Decramer, Mathilde de Menthon, Karine Brochard, Karim Bouchireb, Maud Bezier, Evangeline Pillebout, Fabrice Mihout, Martine Bagot, Olivier Fain, Maya Halabi-Tawil, Agnès Jamin, Philippe Remy, Sonia Azib, Vincent Audard, Monique Dehoux, Jacqueline Rivet, Quentin Raimbourg, Denis Viglietti, Alexis Mathian, Laure Champion, Guillaume Bussone, Bertrand Godeau, Eric Daugas, Anne Saussine-Hickman, Antoine Froissart, Eric Thervet, Elisa Funck-Brentano, Alain Robert, Laureline Berthelot, Nathalie Vittoz, Nicolas Limal, Denis Glotz, Georges Deschênes, Isabelle Halphen, Theresa Kwon, Laurence Vrigneaud, Pierre Housset, Sophie Georgin-Lavialle, Florence Cordoliani, Arsene Mekinian, Virginia Sauvaget, Philippe Grimbert, Jean Christophe Mercier, Philippe Vanhille, Véronique Baudouin, François Vrtovsnik, Agathe Raynaud-Simon, Renato C. Monteiro, Jean-David Bouaziz, Leila Tricot, Laurène Dehoux, Melissa Pierre, Alexandre Karras, Laure Dehen, Céline Lebas, Nathalie Bocquet, Marc Fila, Claire Dossier, Thomas Quemeneur, Maryam Piram, Coralie Bloch-Queyrat, Antoine Dossier, David Verhelst, Anne Maisin, Olivier Benveniste, Dominique Farge, Charlotte Fite, Loïc Guillevin, Rémi Salomon, Emmanuelle Vidal-Petiot, Zahir Amoura, Valérie Caudwell, Assia Smail, Philippe Bouvier, Michel Delahousse, Gentiane Monsel, Jonathan M. Chemouny, Hamza Ayari, Anne-Sophie Verhoeven
Publikováno v:
Nephrology Dialysis Transplantation
Nephrology Dialysis Transplantation, 2017, ⟨10.1093/ndt/gfx300⟩
Nephrology Dialysis Transplantation, Oxford University Press, 2017, ⟨10.1093/ndt/gfx300⟩
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2017, ⟨10.1093/ndt/gfx300⟩
Nephrology Dialysis Transplantation, 2017, ⟨10.1093/ndt/gfx300⟩
Nephrology Dialysis Transplantation, Oxford University Press, 2017, ⟨10.1093/ndt/gfx300⟩
Nephrology Dialysis Transplantation, Oxford University Press (OUP), 2017, ⟨10.1093/ndt/gfx300⟩
Background Henoch-Schonlein purpura, more recently renamed immunoglobulin A vasculitis (IgAV), is a systemic vasculitis characterized by IgA deposits. The current markers used to assess IgAV inaccurately evaluate the risk of nephritis occurrence and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::301434fb3be1c37f73aee774833f24e9
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02445650
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02445650
Autor:
Brigitte Bader-Meunier, Isabelle Halphen, Karen Lambot-Juhan, Nathalie Costedoat-Chalumeau, Martin Chalumeau, Dominique Monnet, Romain K. Gherardi, Christine Barnerias, Christine Bodemer, Jean-Antoine Ribeil
Publikováno v:
Pediatrics. 129:e821-e824
Juvenile dermatomyositis is a rare systemic vasculopathy that may sometimes present with acute complications. We report here the case of a 7-year-old boy with severe dermatomyositis associated with thrombocytopenia and blurry vision. The presence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69e1703b60e498a39af0e3b663d09758
https://doi.org/10.1542/peds.2011-0338
https://doi.org/10.1542/peds.2011-0338
Autor:
Damien Bonnet, Valentine Brousse, Muriel Le Bourgeois, Slimane Allali, Isabelle Halphen, Caroline Elie, Mariane de Montalembert
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 5, p e97462 (2014)
PLoS ONE, Vol 9, Iss 5, p e97462 (2014)
Hypoxia is a common feature in children with sickle cell disease (SCD) that is inconsistently associated with painful crises and acute chest syndrome. To assess the prevalence and risk factors of hypoxia, we recorded daytime, nocturnal, and postexerc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2082bc949296a8b437e0baeba25da836
http://europepmc.org/articles/PMC4039516
http://europepmc.org/articles/PMC4039516
Autor:
Isabelle Halphen, Marie-Laure Franco-Montoya, Pierre-Henri Jarreau, Claude Danan, Fabrice Decobert, Jacques R. Bourbon, Emmanuel Martin, Alice Hadchouel, Olivier Boucherat, Serge Amselem, Alexandra Benachi, Christophe Delacourt
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. 〈10.1371/journal.pone.0003188〉
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Vol 3, Iss 9, p e3188 (2008)
PLoS ONE, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. 〈10.1371/journal.pone.0003188〉
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Vol 3, Iss 9, p e3188 (2008)
PLoS ONE, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
International audience; BACKGOUND: Alveolarization requires coordinated extracellular matrix remodeling, a process in which matrix metalloproteinases (MMPs) play an important role. We postulated that polymorphisms in MMP genes might affect MMP functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566615578b49b7af41337c527c8e1a3c
http://www.hal.inserm.fr/inserm-00447737
http://www.hal.inserm.fr/inserm-00447737
Autor:
Damien Bonnet, Isabelle Halphen, Muriel Le Bourgeois, Mariane de Montalembert, Caroline Elie, Valentine Brousse
Publikováno v:
Blood. 120:4766-4766
Abstract 4766 Background: Respiratory complications are the first causes of death among adult patients with sickle cell anemia (SCA). Finding risk factors for children is important. We study clinical, biological, respiratory and heart parameters, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3259cf76c0156c9ccfba9b24eb18ae8e
https://doi.org/10.1182/blood.v120.21.4766.4766
https://doi.org/10.1182/blood.v120.21.4766.4766