Search Results - Pierre‐François Souchon

  • Showing 1 - 5 results of 5
Refine Results
  1. 1
    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 by 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

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Macroprolactinomas in Children and Adolescents: Factors Associated With the Response to Treatment in 77 Patients

    Macroprolactinomas in Children and Adolescents: Factors Associated With the Response to Treatment in 77 Patients by Sylvie Salenave, Déborah Ancelle, Thibaut Bahougne, Gérald Raverot, Peter Kamenický, Jérôme Bouligand, Anne Guiochon‐Mantel, Agnès Linglart, Pierre‐François Souchon, Marc Nicolino, Jacques Young, Françoise Borson‐Chazot, Brigitte Delemer, Philippe Chanson

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects

    NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects by Florence Roucher‐Boulez, Delphine Mallet-Motak, Dinane Samara‐Boustani, Houweyda Jilani, Asmahane Ladjouze, Pierre‐François Souchon, Dominique Simon, Sylvie Nivot, Claudine Heinrichs, Maryline Ronze, Xavier Bertagna, L. Groisne, Bruno Leheup, Catherine Naud-Saudreau, G Blondin, Christine Lefèvre, Laetitia Lemarchand, Yves Morel

    Published 2016
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    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 by 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

    Published 2014
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    International comparison of glycaemic control in people with type 1 diabetes: an update and extension

    International comparison of glycaemic control in people with type 1 diabetes: an update and extension by Regina Prigge, John McKnight, Sarah H. Wild, Aveni Haynes, Timothy W. Jones, Elizabeth A. Davis, Birgit Rami‐Merhar, Maria Fritsch, Christine Prchla, Astrid Lavens, Kris Doggen, Suchsia Chao, Ronnie Aronson, Ruth E. Brown, Else Helene Ibfelt, Jannet Svensson, Robert J. Young, Justin Warner, Holy Robinson, Tiina Laatikainen, Päivi Rautiainen, Brigitte Delemer, Pierre François Souchon, Alpha Mamadou Diallo, Reinhard W. Holl, Sebastian Schmid, Klemens Raile, Stelios Tigas, Αlexandra Bargiota, Ioanna Zografou, Andrea O. Y. Luk, Juliana C.N. Chan, Seán F. Dinneen, Claire Buckley, Oratile Kgosidialwa, Valentino Cherubini, Rosaria Gesuita, Ieva Strēle, Santa Pildava, Henk J. Veeze, Henk‐Jan Aanstoot, Dick Mul, Craig Jefferies, John G. Cooper, Karianne Fjeld Løvaas, Tadej Battelino, Klemen Dovč, Nataša Bratina, Katarina Eeg‐Olofsson, Ann‐Marie Svensson, Soffia Guðbjörnsdóttir, Evgenia Globa, Nataliya Zelinska

    Published 2021
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: