Resultats de la cerca - Sandrine Compeyrot‐Lacassagne

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  1. 1
    The clinical spectrum of 94 patients carrying a single mutated MEFV allele

    The clinical spectrum of 94 patients carrying a single mutated MEFV allele per Isabelle Koné-Paut, V. Hentgen, S. Guillaume-Czitrom, Sandrine Compeyrot‐Lacassagne, Tú-Anh Tran, Isabelle Touitou

    Publicat 2009
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  2. 2
    Anakinra pharmacokinetics in children and adolescents with systemic-onset juvenile idiopathic arthritis and autoinflammatory syndromes

    Anakinra pharmacokinetics in children and adolescents with systemic-onset juvenile idiopathic arthritis and autoinflammatory syndromes per Saı̈k Urien, Christophe Bardin, Brigitte Bader‐Meunier, Richard Mouy, Sandrine Compeyrot‐Lacassagne, Frantz Foissac, Benoît Florkin, Carine Wouters, Bénédicte Neven, Jean‐Marc Tréluyer, Pierre Quartier

    Publicat 2013
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  3. 3
    A randomised controlled trial of the clinical effectiveness, safety and cost-effectiveness of adalimumab in combination with methotrexate for the treatment of juvenile idiopathic arthritis associated uveitis (SYCAMORE Trial)

    A randomised controlled trial of the clinical effectiveness, safety and cost-effectiveness of adalimumab in combination with methotrexate for the treatment of juvenile idiopathic a... per Athimalaipet V Ramanan, Andrew D. Dick, Diana Benton, Sandrine Compeyrot‐Lacassagne, Dalia Dawoud, Ben Hardwick, Helen Hickey, Dyfrig Hughes, Ashley P Jones, Patricia Woo, Clive Edelsten, Michael W. Beresford

    Publicat 2014
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  4. 4
    Adalimumab plus Methotrexate for Uveitis in Juvenile Idiopathic Arthritis

    Adalimumab plus Methotrexate for Uveitis in Juvenile Idiopathic Arthritis per Athimalaipet V Ramanan, Andrew D. Dick, Ashley P Jones, Andrew McKay, Paula Williamson, Sandrine Compeyrot‐Lacassagne, Ben Hardwick, Helen Hickey, Dyfrig Hughes, Patricia Woo, Diana Benton, Clive Edelsten, Michael W. Beresford

    Publicat 2017
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  5. 5
    100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report

    100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report per Damian Smedley, Katherine R. Smith, A. Martı́n, Ellen A Thomas, Ellen M. McDonagh, Valentina Cipriani, Jamie M. Ellingford, Gavin Arno, Arianna Tucci, Jana Vandrovcová, G. C. Chan, Hywel Williams, Thiloka Ratnaike, Wei Wei, Kathleen Stirrups, Kristina Ibáñez, Loukas Moutsianas, Matthias Wielscher, Anna C. Need, Michael R. Barnes, Letizia Vestito, James Buchanan, Sarah Wordsworth, Sofie Ashford, Karola Rehmström, Emily Li, Gavin Fuller, Philip Twiss, Olivera Spasić-Bošković, Sally Halsall, R. Andres Floto, Kenneth Poole, Annette Wagner, Sarju Mehta, Mark Gurnell, Nigel Burrows, Roger James, Christopher J. Penkett, Eleanor Dewhurst, Stefan Gräf, Rutendo Mapeta, Mary Kasanicki, Andrea Haworth, Helen Savage, Melanie Babcock, Martin G. Reese, Mark Bale, Emma L. Baple, C. R. Boustred, Helen Brittain, Anna de Burca, Marta Bleda, A. Devereau, Dina Halai, Eik Haraldsdottir, Zerin Hyder, Dalia Kasperavičiūtė, Christine Patch, Dimitris Polychronopoulos, Angela Matchan, Răzvan Sultana, Mina Ryten, Ana Lisa Taylor Tavares, Carolyn Tregidgo, Clare Turnbull, M. J. Welland, S. M. Wood, Catherine Snow, Eleanor Williams, S. E. A. Leigh, Rebecca E. Foulger, Louise C. Daugherty, Olivia Niblock, Ivone Leong, Caroline F. Wright, Jim Davies, Charles Crichton, James Welch, Kerrie Woods, Lara Abulhoul, Paul Aurora, Detlef Böckenhauer, Alexander Broomfield, Maureen Cleary, Tanya Lam, Mehul Dattani, Emma Footitt, Vijeya Ganesan, Stephanie Grünewald, Sandrine Compeyrot‐Lacassagne, Francesco Muntoni, Clarissa Pilkington, Rosaline C. M. Quinlivan, Nikhil Thapar, Colin Wallis, Lucy R. Wedderburn, Austen Worth, Teofila Bueser, Cecilia Compton, Charu Deshpande

    Publicat 2021
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