Canlyniadau Chwilio - Anne Pagnier

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  1. 1
    Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema

    Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema gan A. Deroux, Isabelle Boccon‐Gibod, Olivier Fain, P. Pralong, Yann Ollivier, Anne Pagnier, Kamel Djenouhat, A. Du‐Thanh, Anne Gompel, C. Faisant, David Launay, Laurence Bouillet

    Cyhoeddwyd 2016
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  2. 2
    Safety and Efficacy of Rituximab in Severe Juvenile Dermatomyositis: Results from 9 Patients from the French Autoimmunity and Rituximab Registry

    Safety and Efficacy of Rituximab in Severe Juvenile Dermatomyositis: Results from 9 Patients from the French Autoimmunity and Rituximab Registry gan Brigitte Bader‐Meunier, Hélène Decaluwe, Christine Barnérias, Romain K. Gherardi, Pierre Quartier, Albert Faye, Vincent Guigonis, Anne Pagnier, Karine Brochard, Jean Sibilia, Jacques‐Eric Gottenberg, Christine Bodemer

    Cyhoeddwyd 2011
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  3. 3
    Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections

    Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections gan Marie-Hélène Quentien, Brigitte Delemer, Dimitrios T. Papadimitriou, Pierre‐François Souchon, R. Jaussaud, Anne Pagnier, Martine Münzer, Nicolas Jullien, Rachel Reynaud, N. Galon-Faure, A Enjalbert, Anne Barlier, Thierry Brue

    Cyhoeddwyd 2011
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  4. 4
    Standard-Risk Medulloblastoma Treated by Adjuvant Chemotherapy Followed by Reduced-Dose Craniospinal Radiation Therapy: A French Society of Pediatric Oncology Study

    Standard-Risk Medulloblastoma Treated by Adjuvant Chemotherapy Followed by Reduced-Dose Craniospinal Radiation Therapy: A French Society of Pediatric Oncology Study gan V. Oyharcabal-Bourden, C Kalifa, Jean Claude Gentet, Didier Frappaz, C. Edan, Pascal Chastagner, Eric Sariban, Anne Pagnier, A Babin, F. Pichon, S. Neuenschwander, Matthieu Vinchon, D. Bours, Véronique Mosseri, Catherine Le Galès, Marie Madeleine Ruchoux, C. Carrié, François Doz

    Cyhoeddwyd 2005
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  5. 5
    Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

    Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies gan Thierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, Marco Bensa, José‐Mario Capo‐Chichi, Brigitte Delemer, Aurélio Balsalobre, Christina Nassif, Dimitrios T. Papadimitriou, Anne Pagnier, Caroline Hasselmann, Lysanne Patry, Jeremy Schwartzentruber, Pierre‐François Souchon, Shinobu Takayasu, A Enjalbert, Guy Van Vliet, Jacek Majewski, Jacques Drouin, Mark E. Samuels

    Cyhoeddwyd 2014
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  6. 6
    The PRINTO evidence-based proposal for glucocorticoids tapering/discontinuation in new onset juvenile dermatomyositis patients

    The PRINTO evidence-based proposal for glucocorticoids tapering/discontinuation in new onset juvenile dermatomyositis patients gan Gabriella Giancane, Claudio Lavarello, Angela Pistorio, Sheila Knupp Feitosa de Oliveira, Francesco Zulian, Rubén Cuttica, Michel Fischbach, Bo Magnusson, Serena Pastore, Roberto Marini, Silvana Martino, Anne Pagnier, Christine Soler, Valda Staņēvicha, R. ten Cate, Yosef Uziel, Jelena Vojinović, Elena Fueri, Angelo Ravelli, Alberto Martini, Nicolino Ruperto

    Cyhoeddwyd 2019
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  7. 7
    Circulating cell‐free <i>BRAF</i><sup>V600E</sup> as a biomarker in children with Langerhans cell histiocytosis

    Circulating cell‐free <i>BRAF</i><sup>V600E</sup> as a biomarker in children with Langerhans cell histiocytosis gan Sebastien Héritier, Zofia Hélias‐Rodzewicz, Hélène Lapillonne, Nathalie Terrones, Sonia Garrigou, Corinne Normand, Mohamed‐Aziz Barkaoui, Jean Miron, Geneviève Plat, Nathalie Aladjidi, Anne Pagnier, Anne Deville, Marion Gillibert‐Yvert, Despina Moshous, Alain Lefèvre‐Utile, Anne Lutun, Catherine Paillard, Caroline Thomas, Éric Jeziorski, Philippe Nizard, Valérie Taly, Jean‐François Emile, Jean Donadieu

    Cyhoeddwyd 2017
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  8. 8
    Incidence and risk factors for clinical neurodegenerative Langerhans cell histiocytosis: a longitudinal cohort study

    Incidence and risk factors for clinical neurodegenerative Langerhans cell histiocytosis: a longitudinal cohort study gan Sebastien Héritier, Mohamed‐Aziz Barkaoui, Jean Miron, Caroline Thomas, Despina Moshous, Anne Lambilliotte, Françoise Mazingue, Kamila Kébaïli, Éric Jeziorski, Geneviève Plat, Nathalie Aladjidi, Hélène Pacquement, Claire Galambrun, Laurence Brugières, Guy Leverger, L Mansuy, Catherine Paillard, Anne Deville, Anne Pagnier, Anne Lutun, Marion Gillibert‐Yvert, Jean-Louis Stéphan, F. Cohen Aubart, Julien Haroche, Isabelle Pellier, Frédéric Millot, Virginie Gandemer, N. Martin–Duverneuil, Valérie Taly, Zofia Hélias‐Rodzewicz, Jean‐François Emile, Khê Hoang‐Xuan, Ahmed Idbaïh, Jean Donadieu

    Cyhoeddwyd 2018
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  9. 9
    Functional diversity of <i>NLRP3</i> gain-of-function mutants associated with CAPS autoinflammation

    Functional diversity of <i>NLRP3</i> gain-of-function mutants associated with CAPS autoinflammation gan Camille Cosson, Romane Riou, Danish Patoli, Tingting Niu, Amaury Rey, Marine Groslambert, Charlotte de Rosny, Elodie Chatre, Omran Allatif, Thomas Henry, Fabienne Venet, Florian Milhavet, Guilaine Boursier, Alexandre Bélot, Yvan Jamilloux, Étienne Merlin, A. Duquesne, Gilles Grateau, Léa Savey, A. Maria, Anne Pagnier, Solène Poutrel, Olivier Lambotte, Coralie Mallebranche, Samuel Ardois, Olivier Richer, I. Lemelle, Frédéric Rieux‐Laucat, Brigitte Bader‐Meunier, Zahir Amoura, Isabelle Melki, Laurence Cuisset, Isabelle Touitou, Matthias Geyer, Sophie Georgin‐Lavialle, Bénédicte F. Py

    Cyhoeddwyd 2024
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  10. 10
    Molecular and clinicopathologic characterization of pediatric histiocytoses

    Molecular and clinicopathologic characterization of pediatric histiocytoses gan Zofia Hélias‐Rodzewicz, Jean Donadieu, Nathalie Terrones, Mohamed‐Aziz Barkaoui, Anne Lambilliotte, Despina Moshous, Caroline Thomas, Saba Azarnoush, Marlène Pasquet, L Mansuy, Nathalie Aladjidi, Éric Jeziorski, Perrine Marec‐Bérard, Marion Gilibert‐Yvert, Alexandra Spiegel, Paul Saultier, Isabelle Pellier, Anne Pagnier, Sophie Pertuisel, Maryline Poirée, Damien Bodet, Frédéric Millot, Florentina Isfan, Jean-Louis Stéphan, Amaury Leruste, Charlotte Rigaud, Bruno Filhon, Liana Carausu, Yves Réguerre, Isabelle Kieffer, Bénédicte Brichard, Rim Ben Jannet, Mariama Bakari, Ahmed Idbaïh, Christine Bodemer, F. Cohen Aubart, Julien Haroche, Abdellatif Tazi, Sabah Boudjemaa, Sylvie Fraitag, Jean‐François Emile, Sébastien Héritier

    Cyhoeddwyd 2023
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  11. 11
    Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study

    Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study gan Jean Donadieu, Islam Amine Larabi, M. Tardieu, Johannes Visser, Caroline Hutter, Elena Sieni, Nabil Kabbara, Mohamed Barkaoui, Jean Miron, François Chalard, Paul Milne, Julien Haroche, Fleur Cohen, Zofia Hélias‐Rodzewicz, Nicolas Simon, M Jehanne, Alexandra Kolenová, Anne Pagnier, Nathalie Aladjidi, Pascale Schneider, Geneviève Plat, Anne Lutun, Anne Sonntagbauer, Thomas Lehrnbecher, Alina Ferster, Viktoria Efremova, Martina Ahlmann, Laurence Blanc, James C. Nicholson, Anne Lambilliote, Houda Boudiaf, Andrej Lissat, Karel Švojgr, Fanette Bernard, Sarah Elitzur, Michal Golan, D. A. Evseev, Michael Maschan, Ahmed Idbaïh, Olga Slater, Milen Minkov, Valérie Taly, Matthew Collin, Jean‐Claude Alvarez, Jean‐François Emile, Sebastien Héritier

    Cyhoeddwyd 2019
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  12. 12
    Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

    Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts gan Alexandre Bélot, Gillian Rice, Ommar Omarjee, Quentin Rouchon, Eve Smith, Marion Moreews, Maud Tusseau, Cécile Frachette, Raphael Bournhonesque, Nicole M. Thielens, Christine Gaboriaud, Isabelle Rouvet, Emilie Chopin, Akihiro Hoshino, Sylvain Latour, Bruno Ranchin, Rolando Cimaz, Paula Romagnani, Christophe Malcus, Nicole Fabien, Marie-Nathalie Kolopp Sarda, Behrouz Kassaï, Jean‐Christophe Lega, Stéphane Decramer, Pauline Abou-Jaoudé, Ian N Bruce, Thomas Simonet, Claire Bardel, Pierre Antoine Rollat‐Farnier, Sébastien Viel, Héloïse Reumaux, James O’Sullivan, Thierry Walzer, Anne‐Laure Mathieu, Gaëlle Marenne, Thomas Ludwig, Emmanuelle Génin, Jamie M. Ellingford, Brigitte Bader-Meunier, Tracy A. Briggs, Michael W. Beresford, Yanick J. Crow, Dominique Campion, Jean‐François Dartigues, Jean‐François Deleuze, Emmanuelle Génin, Jean‐Charles Lambert, Richard Redon, Emma Allain-Launay, Brigitte Bader‐Meunier, Alexandre Bélot, Kenza Bouayed, Stéphane Burtey, Aurélia Carbasse, Stéphane Decramer, V. Despert, O. Fain, Michel Fischbach, Hugues Flodrops, Caroline Galeotti, Eric Hachulla, Yves Hatchuel, J.F. Kleinmann, Isabelle Koné‐Paut, Aurélia Lanteri, I. Lemelle, Hélène Maillard, François Maurier, Ulrich Meinzer, Isabelle Melki, S. Morell‐Dubois, Anne Pagnier, Maryam Piram, Bruno Ranchin, Héloïse Reumaux, Charlotte Samaille, Jean Sibilia, Olivia Weill, Eslam Al-Abadi, Kate Armon, Kathryn Bailey, Michael W. Beresford, Mary Brennan, Coziana Ciurtin, Janet Gardner‐Medwin, Kirsty Haslam, Daniel Hawley, Alice Leahy, Valentina Leone, Devesh Mewar, Rob Moots, Clarissa Pilkington, Athimalaipet V Ramanan, Satyapal Rangaraj, Annie Ratcliffe, Philip Riley, Ethan S. Sen, Arani Sridhar, Nick Wilkinson, Fiona Wood

    Cyhoeddwyd 2020
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