Torthaí cuardaigh - Gastin, Isabelle

DNA copy number variations in drug reaction with eosinophilia and systemic symptoms (DRESS) identifying 2 new candidates genes de réir Bursztejn, Anne-Claire, Nemos, Christophe, Redon, Richard, Trechot, Philippe, Gastin, Isabelle, Barbaud, Annick

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Compliance with the faecal calprotectin test in patients with inflammatory bowel disease de réir Maréchal, Chloé, Aimone-Gastin, Isabelle, Baumann, Cédric, Dirrenberger, Bastien, Guéant, Jean-Louis, Peyrin-Biroulet, Laurent

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Setting up a Virtual Calprotectin Clinic in Inflammatory Bowel Diseases: Literature Review and Nancy Experience de réir D’Amico, Ferdinando, Netter, Patrick, Baumann, Cedric, Veltin, Muriel, Zallot, Camille, Aimone-Gastin, Isabelle, Danese, Silvio, Peyrin-Biroulet, Laurent

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Diagnostic Accuracy of Procalcitonin for Predicting Blood Culture Results in Patients With Suspected Bloodstream Infection: An Observational Study of 35,343 Consecutive Patients (A... de réir Oussalah, Abderrahim, Ferrand, Janina, Filhine-Tresarrieu, Pierre, Aissa, Nejla, Aimone-Gastin, Isabelle, Namour, Fares, Garcia, Matthieu, Lozniewski, Alain, Guéant, Jean-Louis

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Long-term ACE Inhibitor/ARB Use Is Associated With Severe Renal Dysfunction and Acute Kidney Injury in Patients With Severe COVID-19: Results From a Referral Center Cohort in the N... de réir Oussalah, Abderrahim, Gleye, Stanislas, Clerc Urmes, Isabelle, Laugel, Elodie, Callet, Jonas, Barbé, Françoise, Orlowski, Sophie, Malaplate, Catherine, Aimone-Gastin, Isabelle, Caillierez, Beatrice Maatem, Merten, Marc, Jeannesson, Elise, Kormann, Raphaël, Olivier, Jean-Luc, Rodriguez-Guéant, Rosa-Maria, Namour, Farès, Bevilacqua, Sybille, Losser, Marie-Reine, Levy, Bruno, Kimmoun, Antoine, Gibot, Sébastien, Thilly, Nathalie, Frimat, Luc, Schvoerer, Evelyne, Guéant, Jean-Louis

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The spectrum of biochemical alterations associated with organ dysfunction and inflammatory status and their association with disease outcomes in severe COVID-19: A longitudinal coh... de réir Oussalah, Abderrahim, Gleye, Stanislas, Urmes, Isabelle Clerc, Laugel, Elodie, Barbé, Françoise, Orlowski, Sophie, Malaplate, Catherine, Aimone-Gastin, Isabelle, Caillierez, Beatrice Maatem, Merten, Marc, Jeannesson, Elise, Kormann, Raphaël, Olivier, Jean-Luc, Rodriguez-Guéant, Rosa-Maria, Namour, Farès, Bevilacqua, Sybille, Thilly, Nathalie, Losser, Marie-Reine, Kimmoun, Antoine, Frimat, Luc, Levy, Bruno, Gibot, Sébastien, Schvoerer, Evelyne, Guéant, Jean-Louis

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A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.

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Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.

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