Works matching Raymond Poincaré

Results: 1359
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    MEN OF TODAY.

    Published in:
    1920
    By:
    • Stewart, Jane A.
    Publication type:
    Speech
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    Morbid History.

    Published in:
    History Today, 2006, v. 56, n. 8, p. 2
    By:
    • Grey, Tobias
    Publication type:
    Article
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    THE WEEK IN REVIEW. .

    Published in:
    Journal of Education, 1913, v. 77, n. 5, p. 127, doi. 10.1177/002205741307700508
    Publication type:
    Article
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    The location of DCX mutations predicts malformation severity in X-linked lissencephaly.

    Published in:
    Neurogenetics, 2008, v. 9, n. 4, p. 277, doi. 10.1007/s10048-008-0141-5
    By:
    • Leger, Pierre-Louis;
    • Souville, Isabelle;
    • Boddaert, Nathalie;
    • Elie, Caroline;
    • Pinard, Jean;
    • Plouin, Perrine;
    • Moutard, Marie;
    • Portes, Vincent;
    • Esch, Hilde;
    • Joriot, Sylvie;
    • Renard, Jean;
    • Chelly, Jamel;
    • Francis, Fiona;
    • Beldjord, Cherif;
    • Bahi-Buisson, Nadia
    Publication type:
    Article
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    Can the European abalone Haliotis tuberculata survive on an invasive algae? A comparison of the nutritional value of the introduced Grateloupia turuturu and the native Palmaria palmata, for the commercial European abalone industry.

    Published in:
    Journal of Applied Phycology, 2016, v. 28, n. 4, p. 2427, doi. 10.1007/s10811-015-0741-z
    By:
    • García-Bueno, Nuria;
    • Turpin, Vincent;
    • Cognie, Bruno;
    • Dumay, Justine;
    • Morançais, Michèle;
    • Amat, Mireille;
    • Pédron, Jean-Marie;
    • Atucha, Arnaldo;
    • Fleurence, Joël;
    • Decottignies, Priscilla
    Publication type:
    Article
    36

    STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility.

    Published in:
    Human Mutation, 2018, v. 39, n. 12, p. 1980, doi. 10.1002/humu.23635
    By:
    • Zaharieva, Irina T.;
    • Sarkozy, Anna;
    • Munot, Pinki;
    • Manzur, Adnan;
    • O'Grady, Gina;
    • Rendu, John;
    • Malfatti, Eduardo;
    • Amthor, Helge;
    • Servais, Laurent;
    • Urtizberea, J. Andoni;
    • Neto, Osorio Abath;
    • Zanoteli, Edmar;
    • Donkervoort, Sandra;
    • Taylor, Juliet;
    • Dixon, Joanne;
    • Poke, Gemma;
    • Foley, A. Reghan;
    • Holmes, Chris;
    • Williams, Glyn;
    • Holder, Muriel
    Publication type:
    Article
    37

    Type I hyperprolinemia: genotype/phenotype correlations.

    Published in:
    Human Mutation, 2010, v. 31, n. 8, p. 961, doi. 10.1002/humu.21296
    By:
    • Guilmatre, Audrey;
    • Legallic, Solenn;
    • Steel, Gary;
    • Willis, Alecia;
    • Di Rosa, Gabriella;
    • Goldenberg, Alice;
    • Drouin-Garraud, Valérie;
    • Guet, Agnès;
    • Mignot, Cyril;
    • Des Portes, Vincent;
    • Valayannopoulos, Vassili;
    • Van Maldergem, Lionel;
    • Hoffman, Jodi D.;
    • Izzi, Claudia;
    • Espil-Taris, Caroline;
    • Orcesi, Simona;
    • Bonafé, Luisa;
    • Le Galloudec, Eric;
    • Maurey, Hélène;
    • Ioos, Christine
    Publication type:
    Article
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    Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores.

    Published in:
    Human Mutation, 2008, v. 29, n. 5, p. 670, doi. 10.1002/humu.20696
    By:
    • Monnier, Nicole;
    • Marty, Isabelle;
    • Faure, Julien;
    • Castiglioni, Claudia;
    • Desnuelle, Claude;
    • Sacconi, Sabrina;
    • Estournet, Brigitte;
    • Ferreiro, Ana;
    • Romero, Norma;
    • Laquerriere, Annie;
    • Lazaro, Leila;
    • Martin, Jean-Jacques;
    • Morava, Eva;
    • Rossi, Annick;
    • Van der Kooi, Anneke;
    • de Visser, Marianne;
    • Verschuuren, Corien;
    • Lunardi, Joël
    Publication type:
    Article
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