يعرض 1 - 10 نتائج من 55 نتيجة بحث عن '"Decamp, Matthieu"', وقت الاستعلام: 1.06s تنقيح النتائج
  1. 1
    دورية أكاديمية
    French guidelines for the etiological workup of eosinophilia and the management of hypereosinophilic syndromes

    المؤلفون: Groh, MatthieuAff1, Aff2, Aff3, Aff36, IDs13023023026964_cor1, Rohmer, JulienAff1, Aff4, Aff36, Etienne, NicolasAff5, Aff36, Abou Chahla, WadihAff1, Aff6, Aff36, Baudet, AntoineAff1, Aff7, Aff36, Chan Hew Wai, AurélieAff1, Aff8, Aff36, Chenivesse, CécileAff1, Aff9, Aff10, Aff36, Clisson Rusek, IrenaAff11, Aff36, Cottin, VincentAff12, Aff36, Decamp, MatthieuAff13, Aff36, De Groote, PascalAff1, Aff14, Aff36, Delahousse, FannyAff15, Aff36, Duployez, NicolasAff1, Aff16, Aff17, Aff36, Faguer, StanislasAff18, Aff36, Gottrand, FrédéricAff1, Aff3, Aff19, Aff36, Huang, FlorentAff1, Aff20, Aff36, Leblanc, ThierryAff21, Aff36, Magnan, AntoineAff1, Aff22, Aff36, Martin, ThierryAff1, Aff23, Aff36, Mortuaire, GeoffreyAff1, Aff3, Aff24, Aff36, Néel, AntoineAff1, Aff25, Aff36, Paris, LucAff26, Aff36, Petit, ArnaudAff27, Aff36, Rossignol, JulienAff28, Aff36, Schleinitz, NicolasAff1, Aff29, Aff36, Soret-Dulphy, JulietteAff30, Aff36, Staumont-Salle, DelphineAff1, Aff31, Aff36, Terrier, BenjaminAff32, Aff36, Terriou, LouisAff1, Aff33, Aff36, Viallard, Jean-FrançoisAff1, Aff34, Aff36, Lefèvre, GuillaumeAff1, Aff3, Aff33, Aff34, Aff36, Kahn, Jean-EmmanuelAff1, Aff35, Aff36

    المصدر: Orphanet Journal of Rare Diseases. 18(1)

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  2. 2
    دورية أكاديمية
    Cytogenetics in the management of myeloproliferative neoplasms, mastocytosis and myelodysplastic/myeloproliferative neoplasms: Guidelines from the Group Francophone de Cytogénétique Hématologique (GFCH)

    المؤلفون: Decamp, Matthieu, Klein, Emilie, Godon, Catherine, Lestringant, Valentin, Roynard, Pauline, Theisen, Olivier, Jimenez-Pocquet, Mélanie, Roche-Lestienne, Catherine, Bidet, Audrey, Veronese, Lauren

    المصدر: In Current Research in Translational Medicine October-December 2023 71(4)

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  3. 3
    دورية أكاديمية
    Cytogenetics in the management of acute myeloid leukemia and histiocytic/dendritic cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH)

    المؤلفون: Bidet, Audrey, Quessada, Julie, Cuccuini, Wendy, Decamp, Matthieu, Lafage-Pochitaloff, Marina, Luquet, Isabelle, Lefebvre, Christine, Tueur, Giulia

    المصدر: In Current Research in Translational Medicine October-December 2023 71(4)

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  4. 4
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  5. 5
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  6. 6
    دورية أكاديمية
    High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B

    المؤلفون: Colson, Cindy, Decamp, Matthieu, Gruchy, Nicolas, Coudray, Nadia, Ballandonne, Céline, Bracquemart, Claire, Molin, Arnaud, Mittre, Hervé, Takatani, Rieko, Jüppner, Harald, Kottler, Marie-Laure, Richard, Nicolas

    المصدر: In Bone June 2019 123:145-152

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  7. 7
    دورية أكاديمية
    15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients

    المؤلفون: Vanlerberghe, Clémence, Petit, Florence, Malan, Valérie, Vincent-Delorme, Catherine, Bouquillon, Sonia, Boute, Odile, Holder-Espinasse, Muriel, Delobel, Bruno, Duban, Bénédicte, Vallee, Louis, Cuisset, Jean-Marie, Lemaitre, Marie-Pierre, Vantyghem, Marie-Christine, Pigeyre, Marie, Lanco-Dosen, Sandrine, Plessis, Ghislaine, Gerard, Marion, Decamp, Matthieu, Mathieu, Michèle, Morin, Gilles, Jedraszak, Guillaume, Bilan, Frédéric, Gilbert-Dussardier, Brigitte, Fauvert, Delphine, Roume, Joëlle, Cormier-Daire, Valérie, Caumes, Roseline, Puechberty, Jacques, Genevieve, David, Sarda, Pierre, Pinson, Lucie, Blanchet, Patricia, Lemeur, Nathalie, Sheth, Frenny, Manouvrier-Hanu, Sylvie, Andrieux, Joris

    المصدر: In European Journal of Medical Genetics March 2015 58(3):140-147

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  8. 8
    دورية أكاديمية
    21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders

    المؤلفون: Petit, Florence, Plessis, Ghislaine, Decamp, Matthieu, Cuisset, Jean-Marie, Blyth, Moira, Pendlebury, Maria, Andrieux, Joris

    المصدر: In European Journal of Medical Genetics January 2015 58(1):44-46

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  9. 9
    دورية أكاديمية

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  10. 10
    دورية أكاديمية

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