يعرض 1 - 10 نتائج من 52 نتيجة بحث عن '"Mathieu Fiore"', وقت الاستعلام: 0.91s 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: Mathieu Fiore, Janine-Sophie Giraudet, Marie-Christine Alessi, Céline Falaise, Dominique Desprez, Roseline d’Oiron, Sophie Voisin, Marie-Françoise Hurtaud, Hélène Boutroux, Paul Saultier, Cécile Lavenu-Bombled, Gilles Bagou, Xavier Dubucs, Anthony Chauvin, Christophe Leroy, Francine Meckert, François Kerbaul, Nicolas Giraud, Ambra Pühler, Ana Rath

    المصدر: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)

    مصطلحات موضوعية: Medicine

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1750-1172

    URL الوصول: https://doaj.org/article/afdd1c0969c24287ad8dac6e3b9a780a

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  2. 2
    دورية أكاديمية
    A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies

    المؤلفون: Vincent Michaud, Mathieu Fiore, Valentine Coste, Yoann Huguenin, Jean-Claude Bordet, Claudio Plaisant, Eulalie Lasseaux, Fanny Morice-Picard, Benoit Arveiler

    المصدر: Platelets, Vol 32, Iss 3, Pp 420-423 (2021)

    مصطلحات موضوعية: albinism, hermansky-pudlak syndrome, Diseases of the blood and blood-forming organs, RC633-647.5

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/0953-7104; https://doaj.org/toc/1369-1635

    URL الوصول: https://doaj.org/article/37c16417a07a4e8490be55cb12d5e62f

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  3. 3
    دورية أكاديمية
    Successful management of a pregnant woman with severe ANKRD26-related thrombocytopenia and anti-HPA-5b alloimmunization

    المؤلفون: Estibaliz Lazaro, Clémence Houssin, Loic Sentilhes, Laura Blouin, Mathieu Fiore

    المصدر: Platelets, Vol 31, Iss 6, Pp 827-829 (2020)

    مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/0953-7104; https://doaj.org/toc/1369-1635

    URL الوصول: https://doaj.org/article/ba32d8c1067c4fcbb95086f052f0f1ec

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  4. 4
    دورية أكاديمية
    Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34+ progenitors

    المؤلفون: Marjorie Poggi, Matthias Canault, Marie Favier, Ernest Turro, Paul Saultier, Dorsaf Ghalloussi, Veronique Baccini, Lea Vidal, Anna Mezzapesa, Nadjim Chelghoum, Badreddine Mohand-Oumoussa, Céline Falaise, Rémi Favier, Willem H. Ouwehand, Mathieu Fiore, Franck Peiretti, Pierre Emmanuel Morange, Noémie Saut, Denis Bernot, Andreas Greinacher, NIHR BioResource, Alan T. Nurden, Paquita Nurden, Kathleen Freson, David-Alexandre Trégouët, Hana Raslova, Marie-Christine Alessi

    المصدر: Haematologica, Vol 102, Iss 2 (2017)

    مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

    وصف الملف: electronic resource

    Relation: https://haematologica.org/article/view/7968; https://doaj.org/toc/0390-6078; https://doaj.org/toc/1592-8721

    URL الوصول: https://doaj.org/article/373f87248f02458bb1797cfbb7fb7965

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  5. 5
    HemosIL VWF:GPIbR Assay Has a Greater Sensitivity than VWF:RCo Technique to Detect Acquired von Willebrand Syndrome in Myeloproliferative Neoplasms

    المؤلفون: Pierre Laporte, Marie Tuffigo, Anne Ryman, Mathieu Fiore, Etienne Rivière, Chloé James, Alexandre Guy

    المصدر: Thrombosis and Haemostasis. 122:1673-1682

    مصطلحات موضوعية: Thrombocytosis, von Willebrand Diseases, congenital, hereditary, and neonatal diseases and abnormalities, Neoplasms, hemic and lymphatic diseases, von Willebrand Factor, cardiovascular system, Humans, Collagen, Hematology, circulatory and respiratory physiology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d7420f083423230e9484b9dfefe4473
    https://doi.org/10.1055/a-1806-9972

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  6. 6
    Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest Study

    المؤلفون: Justine Hugon-Rodin, Camille Carrière, Ségolène Claeyssens, Nathalie Trillot, Nicolas Drillaud, Christine Biron-Andreani, Cécile Lavenu-Bombled, Anna Wieland, Claire Flaujac, Natalie Stieltjes, Aurélien Lebreton, Thomas Brungs, Andrea Hegglin, Mathieu Fiore, Céline Desconclois, Valérie Gay, Brigitte Tardy-Poncet, Philippe Beurrier, Virginie Barbay, Pierre Chamouni, Emmanuel De Maistre, Tomas Simurda, Alessandro Casini

    مصطلحات موضوعية: Hematology, 610 Medicine & health

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e0f4e913709c7a5ad5af681f0553bf4

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  7. 7
    Atypical late diagnosis of Noonan syndrome revealed by bleedings due to platelet dysfunction

    المؤلفون: Sabine-Marie Castet, Mathieu Fiore, Marie-Christine Alessi, Sophie Naudion, Jean-Claude Bordet

    المساهمون: Biologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases, Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Université de Bordeaux (UB)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

    المصدر: Journal of Thrombosis and Thrombolysis
    Journal of Thrombosis and Thrombolysis, Springer Verlag (Germany), 2021
    Journal of Thrombosis and Thrombolysis, 2021

    مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Delayed Diagnosis, Platelet dysfunction, MEDLINE, Hemorrhage, 030204 cardiovascular system & hematology, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Humans, Medicine, ComputingMilieux_MISCELLANEOUS, 030304 developmental biology, 0303 health sciences, Hematology, business.industry, Noonan Syndrome, medicine.disease, 3. Good health, Late diagnosis, Mutation, Noonan syndrome, Cardiology and Cardiovascular Medicine, business, Recherches cliniques, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d15a3c50af1fe9de4159cf647774912
    https://doi.org/10.1007/s11239-021-02547-8

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  8. 8
    Platelet function studies in myeloproliferative neoplasms patients with Calreticulin or JAK2V617F mutation

    المؤلفون: Alexandre Guy, Khalil Helzy, Olivier Mansier, Jean-Claude Bordet, Etienne Rivière, Mathieu Fiore, Chloe James

    المصدر: Research and Practice in Thrombosis and Haemostasis. 7:100060

    مصطلحات موضوعية: Hematology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f49215a7be5cc8defd84c308fb42fbb3
    https://doi.org/10.1016/j.rpth.2023.100060

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  9. 9
    Immunization against αIIbβ3 and αvβ3 in Glanzmann thrombasthenia patients carrying the French Gypsy mutation

    المؤلفون: Laura Blouin, Roongaroon Phuangtham, Mathieu Fiore, Sentot Santoso, Yoann Huguenin, Gregor Bein, Behnaz Bayat

    المصدر: Journal of Thrombosis and Haemostasis. 19:255-261

    مصطلحات موضوعية: endocrine system, Mutation, biology, business.industry, Integrin, Hematology, Transfection, 030204 cardiovascular system & hematology, medicine.disease_cause, medicine.disease, Epitope, 3. Good health, Platelet transfusion refractoriness, 03 medical and health sciences, 0302 clinical medicine, Neonatal alloimmune thrombocytopenia, Immunology, medicine, biology.protein, Platelet, business, hormones, hormone substitutes, and hormone antagonists, ITGA2B Gene

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::24cf669e25d37f7c03fa6b564020c6a7
    https://doi.org/10.1111/jth.15117

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  10. 10
    BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome

    المؤلفون: Angèle Tingaud-Sequeira, Cédric Delevoye, Vincent Michaud, Anne Bauters, Perrine Pennamen, Benoit Arveiler, Nguyen Van Duong Béatrice, V. Coste, Linh Le, Eulalie Lasseaux, Claudio Plaisant, Fanny Morice Picard, Modibo Diallo, Aurélien Trimouille, Jean-Claude Bordet, Bruno Delobel, Mathieu Fiore, Didier Lacombe, Michael S. Marks

    المصدر: Genet Med

    مصطلحات موضوعية: Genetics, Candidate gene, Mutation, Biology, medicine.disease, medicine.disease_cause, Oculocutaneous albinism, Article, eye diseases, Human genetics, Bleeding diathesis, hemic and lymphatic diseases, medicine, Albinism, Hermansky–Pudlak syndrome, Allele, Genetics (clinical)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda30ebffaaece874e26abdf228a51df
    https://doi.org/10.1038/s41436-020-0867-5

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