Works matching Raymond Poincaré

Results: 1347
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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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    MEN OF TODAY.

    Published in:
    1920
    By:
    • Stewart, Jane A.
    Publication type:
    Speech
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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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    Galectin-3: a novel biomarker of glycogen storage disease type III.

    Published in:
    Cell Death Discovery, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41420-025-02452-6
    By:
    • Rossiaud, Lucille;
    • Miagoux, Quentin;
    • Benabides, Manon;
    • Reiss, Océane;
    • Jauze, Louisa;
    • Jarrige, Margot;
    • Polvèche, Hélène;
    • Malfatti, Edoardo;
    • Laforêt, Pascal;
    • Ronzitti, Giuseppe;
    • Nissan, Xavier;
    • Hoch, Lucile
    Publication type:
    Article
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    Status of Sepsis Care in European Hospitals: Results from an International Cross-Sectional Survey.

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2025, v. 211, n. 4, p. 587, doi. 10.1164/rccm.202406-1167OC
    By:
    • Scheer, Christian S.;
    • Giamarellos-Bourboulis, Evangelos J.;
    • Ferrer, Ricard;
    • Idelevich, Evgeny A.;
    • Annane, Djillali;
    • Artigas, Antonio;
    • Aslan, Abdullah Tarik;
    • Bottari, Gabriella;
    • Bouma, Hjalmar R.;
    • Černý, Vladimir;
    • Curić Radivojević, Renata;
    • Dakou, Konstantina;
    • Dewitte, Ken;
    • Elbahnasawy, Mohamed;
    • Gründling, Matthias;
    • Gurjar, Mohan;
    • Hästbacka, Johanna;
    • Kyprianou, Miltiadis;
    • Laribi, Said;
    • Lassen, Annmarie
    Publication type:
    Article
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    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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    Outpatient total ankle replacement.

    Published in:
    International Orthopaedics, 2021, v. 45, n. 9, p. 2429, doi. 10.1007/s00264-021-05140-z
    By:
    • Sadoun, Maxime;
    • Hardy, Alexandre;
    • Cladière, Victoire;
    • Guichard, Leah;
    • Bauer, Thomas;
    • Stiglitz, Yves
    Publication type:
    Article
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    ACTN2 mutations cause "Multiple structured Core Disease" (MsCD).

    Published in:
    Acta Neuropathologica, 2019, v. 137, n. 3, p. 501, doi. 10.1007/s00401-019-01963-8
    By:
    • Lornage, Xavière;
    • Romero, Norma B.;
    • Grosgogeat, Claire A.;
    • Malfatti, Edoardo;
    • Donkervoort, Sandra;
    • Marchetti, Michael M.;
    • Neuhaus, Sarah B.;
    • Foley, A. Reghan;
    • Labasse, Clémence;
    • Schneider, Raphaël;
    • Carlier, Robert Y.;
    • Chao, Katherine R.;
    • Medne, Livija;
    • Deleuze, Jean-François;
    • Orlikowski, David;
    • Bönnemann, Carsten G.;
    • Gupta, Vandana A.;
    • Fardeau, Michel;
    • Böhm, Johann;
    • Laporte, Jocelyn
    Publication type:
    Article