يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Fiore, Mathieu"', وقت الاستعلام: 0.75s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.

    المؤلفون: Fiore, Mathieu1,2 (AUTHOR) mathieu.fiore@chu-bordeaux.fr, Giraudet, Janine-Sophie3 (AUTHOR), Alessi, Marie-Christine4,5 (AUTHOR), Falaise, Céline5,6 (AUTHOR), Desprez, Dominique7 (AUTHOR), d'Oiron, Roseline8 (AUTHOR), Voisin, Sophie9 (AUTHOR), Hurtaud, Marie-Françoise10 (AUTHOR), Boutroux, Hélène11 (AUTHOR), Saultier, Paul5,12 (AUTHOR), Lavenu-Bombled, Cécile13 (AUTHOR), Bagou, Gilles14 (AUTHOR), Dubucs, Xavier15 (AUTHOR), Chauvin, Anthony16 (AUTHOR), Leroy, Christophe17 (AUTHOR), Meckert, Francine18 (AUTHOR), Kerbaul, François18 (AUTHOR), Giraud, Nicolas19 (AUTHOR), Pühler, Ambra3 (AUTHOR), Rath, Ana3 (AUTHOR)

    المصدر: Orphanet Journal of Rare Diseases. 6/29/2023, Vol. 18 Issue 1, p1-8. 8p.

    مصطلحات موضوعية: *EMERGENCY management, *LITERATURE reviews, *BLOOD platelets, *MEDICAL personnel, *BLOOD platelet aggregation, *GENETIC disorders, *THROMBIN receptors, *CHILDBIRTH, *THROMBOPOIETIN receptors

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  2. 2
    دورية أكاديمية
    A diagnostic approach that may help to discriminate inherited thrombocytopenia from chronic immune thrombocytopenia in adult patients.

    المؤلفون: Fiore, Mathieu1,2 (AUTHOR) mathieu.fiore@chu-bordeaux.fr, Pillois, Xavier2 (AUTHOR), Lorrain, Simon3 (AUTHOR), Bernard, Marie-Agnès3 (AUTHOR), Moore, Nicholas3 (AUTHOR), Sié, Pierre2,4 (AUTHOR), Viallard, Jean-François5 (AUTHOR), Nurden, Paquita2,6 (AUTHOR)

    المصدر: Platelets. Sep2016, Vol. 27 Issue 6, p555-562. 8p.

    مصطلحات موضوعية: *THROMBOCYTOPENIA, *IMMUNOLOGIC diseases, *GENETIC disorders, *BLOOD platelets, *ELECTRON microscopy, *DIAGNOSIS


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  3. 3
    دورية أكاديمية
    A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.

    المؤلفون: Ng, Bobby G.1 (AUTHOR), Sosicka, Paulina1 (AUTHOR), Fenaille, François2 (AUTHOR), Harroche, Annie3 (AUTHOR), Vuillaumier-Barrot, Sandrine4,5 (AUTHOR), Porterfield, Mindy6 (AUTHOR), Xia, Zhi-Jie1 (AUTHOR), Wagner, Shannon6 (AUTHOR), Bamshad, Michael J.7,8 (AUTHOR), Vergnes-Boiteux, Marie-Christine9 (AUTHOR), Cholet, Sophie2 (AUTHOR), Dalton, Stephen10,11 (AUTHOR), Dell, Anne12 (AUTHOR), Dupré, Thierry4 (AUTHOR), Fiore, Mathieu9,13 (AUTHOR), Haslam, Stuart M.12 (AUTHOR), Huguenin, Yohann14 (AUTHOR), Kumagai, Tadahiro6 (AUTHOR), Kulik, Michael10,11 (AUTHOR), McGoogan, Katherine15 (AUTHOR)

    المصدر: American Journal of Human Genetics. Jun2021, Vol. 108 Issue 6, p1040-1052. 13p.

    مصطلحات موضوعية: *CONGENITAL disorders, *GENETIC disorders, *GLYCOSYLATION, *GENETIC variation, *LIVER, *GLUCOSE-regulated proteins

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