Kết quả tìm kiếm - Anthony Oojageer

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  1. 1
    Stimulator of Interferon Genes–Associated Vasculopathy With Onset in Infancy

    Stimulator of Interferon Genes–Associated Vasculopathy With Onset in Infancy Bằng J Conde Munoz, M. Rodière, Nadia Jeremiah, Frédéric Rieux‐Laucat, Anthony Oojageer, Gillian Rice, Flore Rozenberg, Yanick J. Crow, D. Bessis

    Được phát hành 2015
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    Artigo
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  2. 2
    Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease

    Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease Bằng Gillian Rice, Isabelle Melki, Marie‐Louise Frémond, Tracy A. Briggs, Mathieu P. Rodero, Naoki Kitabayashi, Anthony Oojageer, Brigitte Bader‐Meunier, Alexandre Bélot, Christine Bodemer, Pierre Quartier, Yanick J. Crow

    Được phát hành 2016
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    Artigo
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  3. 3
    Mutations in CECR1 associated with a neutrophil signature in peripheral blood

    Mutations in CECR1 associated with a neutrophil signature in peripheral blood Bằng Alexandre Bélot, Evangeline Wassmer, Marinka Twilt, Jean‐Christophe Lega, Leo Zeef, Anthony Oojageer, Paul R. Kasher, Anne‐Laure Mathieu, Christophe Malcus, Julie Demaret, Nicole Fabien, Sophie Collardeau‐Frachon, Laura Mechtouff, Laurent Derex, Thierry Walzer, Gillian Rice, I. Durieu, Yanick J. Crow

    Được phát hành 2014
    lấy văn bản lấy văn bản
    Artigo
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  4. 4
    Unusual cutaneous features associated with a heterozygous gain-of-function mutation in<i>IFIH1</i>: overlap between Aicardi-Goutières and Singleton-Merten syndromes

    Unusual cutaneous features associated with a heterozygous gain-of-function mutation in<i>IFIH1</i>: overlap between Aicardi-Goutières and Singleton-Merten syndromes Bằng A.‐C. Bursztejn, Tracy A. Briggs, Yoandris del Toro Duany, Bryan Anderson, James O’Sullivan, Simon G. Williams, Christine Bodemer, Sylvie Fraïtag, Florian Gebhard, Bruno Leheup, I. Lemelle, Anthony Oojageer, Emmanuel Raffo, Emmanuelle Schmitt, Gillian Rice, Sun Hur, Yanick J. Crow

    Được phát hành 2015
    lấy văn bản
    Artigo
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  5. 5
    Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

    Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts Bằng Emma M. Jenkinson, Mathieu P. Rodero, Paul R. Kasher, Carolina Uggenti, Anthony Oojageer, Laurence Goosey, Y Rose, Christopher J. Kershaw, Jill Urquhart, Simon G. Williams, Sanjeev S. Bhaskar, James D.B. O’Sullivan, Gabriela M. Baerlocher, Monika Haubitz, Geraldine Aubert, Kristin Barañano, Angela Barnicoat, Roberta Battini, Andrea Berger, Edward Blair, Janice Brunstrom-Hernandez, Johannes Buckard, David Cassiman, Rosaline Caumes, Duccio Maria Cordelli, Liesbeth M De Waele, Alexander Fay, Patrick Ferreira, Nicholas Fletcher, Alan Fryer, Himanshu Goel, Cheryl Hemingway, Marco Henneke, Imelda Hughes, Rosalind J Jefferson, Ram Kumar, Lieven Lagae, P. Landrieu, Charles Marques Lourenço, Timothy J Malpas, Sarju Mehta, Imke Metz, SakkuBai Naidu, Katrin Õunap, Axel Panzer, Prab Prabhakar, Gerardine Quaghebeur, Raphael Schiffmann, Elliott H. Sherr, Kanaga R Sinnathuray, Calvin Soh, Helen Stewart, Jon Stone, Hilde Van Esch, Christine E G Van Mol, Adeline Vanderver, Emma Wakeling, Andrea Whitney, Graham D. Pavitt, Sam Griffiths‐Jones, Gillian Rice, Patrick Revy, Marjo S. van der Knaap, John H. Livingston, Raymond T. O’Keefe, Yanick J. Crow

    Được phát hành 2016
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    Artigo
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  6. 6
    Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

    Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1<... Bằng Yanick J. Crow, Diana Chase, Johanna L. Schmidt, Marcin Szynkiewicz, Gabriella Forte, Hannah Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine S. W. Albin, Stavit A. Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul‐Hirji, Eileen Baildam, Nadia Bahi‐Buisson, Kathryn Bailey, Christine Barnérias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez

    Được phát hành 2015
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    Artigo
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