Hasil Pencarian - Caroline Deswarte

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  1. 1
    Le mémorial du Canada à Vimy de Parcs Canada

    Le mémorial du Canada à Vimy de Parcs Canada oleh Caroline Deswarte

    Diterbitkan 2016-12-01
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  2. 2
    A novel variant in the neutrophil cytosolic factor 2 (NCF2) gene results in severe disseminated BCG infectious disease: A clinical report and literature review

    A novel variant in the neutrophil cytosolic factor 2 (NCF2) gene results in severe disseminated BCG infectious disease: A clinical report and literature review oleh Suzan A. AlKhater, Caroline Deswarte, Jean‐Laurent Casanova, Jacinta Bustamante

    Diterbitkan 2020-06-01
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  3. 3
    Skewed X-inactivation in a Female Carrier with X-linked Chronic Granulomatous Disease

    Skewed X-inactivation in a Female Carrier with X-linked Chronic Granulomatous Disease oleh Itzel López-Hernández, Caroline Deswarte, Miguel Ángel Alcantara-Ortigoza, María del Mar Saez-de-Ocariz, Marco Antonio Yamazaki-Nakashimada, Sara Elva Espinosa-Padilla, Jacinta Bustamante, Lizbeth Blancas-Galicia

    Diterbitkan 2019-08-01
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  4. 4
    Homeobox protein TLX3 activates miR-125b expression to promote T-cell acute lymphoblastic leukemia

    Homeobox protein TLX3 activates miR-125b expression to promote T-cell acute lymphoblastic leukemia oleh Laurent Renou, Pierre-Yves Boelle, Caroline Deswarte, Salvatore Spicuglia, Aissa Benyoucef, Julien Calvo, Benjamin Uzan, Mohamed Belhocine, Agata Cieslak, Judith Landman-Parker, Andre Baruchel, Vahid Asnafi, Françoise Pflumio, Paola Ballerini, Irina Naguibneva

    Diterbitkan 2017-05-01
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  5. 5
    Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature

    Multifocal Recurrent Osteomyelitis and Hemophagocytic Lymphohistiocytosis in a Boy with Partial Dominant IFN-γR1 Deficiency: Case Report and Review of the Literature oleh Aidé Tamara Staines-Boone, Caroline Deswarte, Edna Venegas Montoya, Edna Venegas Montoya, Luz María Sánchez-Sánchez, Jorge Alberto García Campos, Teodoro Muñiz-Ronquillo, Jacinta Bustamante, Francisco J. Espinosa-Rosales, Saul Oswaldo Lugo Reyes

    Diterbitkan 2017-05-01
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  6. 6
    Multi-target measurable residual disease assessed by error-corrected sequencing in patients with acute myeloid leukemia: An ALFA study

    Multi-target measurable residual disease assessed by error-corrected sequencing in patients with acute myeloid leukemia: An ALFA study oleh Pierre Hirsch, Jérôme Lambert, Maxime Bucci, Caroline Deswarte, Augustin Boudry, Juliette Lambert, Laurene Fenwarth, Jean-Baptiste Micol, Christine Terré, Karine Celli-Lebras, Xavier Thomas, Hervé Dombret, Nicolas Duployez, Claude Preudhomme, Raphael Itzykson, Francois Delhommeau

    Diterbitkan 2024-06-01
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  7. 7
    Novel mutations in NCF4 gene confer non-classic chronic granulomatous disease with disseminated histoplasmosis in a Colombian child

    Novel mutations in NCF4 gene confer non-classic chronic granulomatous disease with disseminated histoplasmosis in a Colombian child oleh Carlos Andrés Arango-Franco, Alejandro Nieto-Patlán, Marcela Moncada-Vélez, Jesús Armando Álvarez, Carmen Oleaga-Quinta, Caroline Deswarte, Juan Fernando Alzate, Felipe Cabarcas, Carlos Garcés, Julio César Orrego, Susana Pamela Mejía, Luz Elena Cano, Jean-Laurent Casanova, Jacinta Bustamante, José Luis Franco, Andrés Augusto Arias

    Diterbitkan 2018-06-01
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  8. 8
    Interleukin‐18 produced by bone marrow‐derived stromal cells supports T‐cell acute leukaemia progression

    Interleukin‐18 produced by bone marrow‐derived stromal cells supports T‐cell acute leukaemia progression oleh Benjamin Uzan, Sandrine Poglio, Bastien Gerby, Ching‐Lien Wu, Julia Gross, Florence Armstrong, Julien Calvo, Xavier Cahu, Caroline Deswarte, Florent Dumont, Diana Passaro, Corinne Besnard‐Guérin, Thierry Leblanc, André Baruchel, Judith Landman‐Parker, Paola Ballerini, Véronique Baud, Jacques Ghysdael, Frédéric Baleydier, Francoise Porteu, Francoise Pflumio

    Diterbitkan 2014-06-01
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  9. 9
    IRF4 haploinsufficiency in a family with Whipple’s disease

    IRF4 haploinsufficiency in a family with Whipple’s disease oleh Antoine Guérin, Gaspard Kerner, Nico Marr, Janet G Markle, Florence Fenollar, Natalie Wong, Sabri Boughorbel, Danielle T Avery, Cindy S Ma, Salim Bougarn, Matthieu Bouaziz, Vivien Béziat, Erika Della Mina, Carmen Oleaga-Quintas, Tomi Lazarov, Lisa Worley, Tina Nguyen, Etienne Patin, Caroline Deswarte, Rubén Martinez-Barricarte, Soraya Boucherit, Xavier Ayral, Sophie Edouard, Stéphanie Boisson-Dupuis, Vimel Rattina, Benedetta Bigio, Guillaume Vogt, Frédéric Geissmann, Lluis Quintana-Murci, Damien Chaussabel, Stuart G Tangye, Didier Raoult, Laurent Abel, Jacinta Bustamante, Jean-Laurent Casanova

    Diterbitkan 2018-03-01
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