Ohcanbohtosat - G Morin

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  1. 1
    Evaluation of current methods for creatine kinase isoenzyme fractionation.

    Evaluation of current methods for creatine kinase isoenzyme fractionation. Dahkki L G Morin

    Almmustuhtton 1977
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  2. 2
    Single Glucose Oxidase—Peroxidase Reagent for Two-Minute Determination of Serum Glucose

    Single Glucose Oxidase—Peroxidase Reagent for Two-Minute Determination of Serum Glucose Dahkki L G Morin, Jerome Prox

    Almmustuhtton 1973
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    Artigo
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  3. 3
    Luminous Enteric Bacteria of Marine Fishes: a Study of Their Distribution, Densities, and Dispersion

    Luminous Enteric Bacteria of Marine Fishes: a Study of Their Distribution, Densities, and Dispersion Dahkki Edward G. Ruby, James G. Morin

    Almmustuhtton 1979
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  4. 4
    Non-enzymic glycation of individual plasma proteins in normoglycemic and hyperglycemic patients.

    Non-enzymic glycation of individual plasma proteins in normoglycemic and hyperglycemic patients. Dahkki Garth E. Austin, Richard H. Mullins, L G Morin

    Almmustuhtton 1987
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    Artigo
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  5. 5
    DNA methylation of channel-related genes in cancers

    DNA methylation of channel-related genes in cancers Dahkki Halima Ouadid‐Ahidouch, Lise Rodat‐Despoix, Fabrice Matifat, G Morin, Ahmed Ahidouch

    Almmustuhtton 2015
    Viečča ollesdeavstta
    Revisão
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  6. 6
    Impact of Blood Pressure Dysregulation on Health-Related Quality of Life in Persons With Spinal Cord Injury: Development of a Conceptual Model

    Impact of Blood Pressure Dysregulation on Health-Related Quality of Life in Persons With Spinal Cord Injury: Development of a Conceptual Model Dahkki Noelle E. Carlozzi, Denise Fyffe, Kel G. Morin, Rachel Byrne, David S. Tulsky, David Victorson, Jin‐Shei Lai, Jill M. Wecht

    Almmustuhtton 2013
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    Artigo
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  7. 7
    A Population-Based Analysis of the Relationship Between Substance Use and Adolescent Cognitive Development

    A Population-Based Analysis of the Relationship Between Substance Use and Adolescent Cognitive Development Dahkki Jean-François G. Morin, Mohammad H. Afzali, Josiane Bourque, Sherry H. Stewart, Jean R. Séguin, Maeve O’Leary-Barrett, Patricia Conrod

    Almmustuhtton 2018
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    Artigo
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  8. 8
    <i>TCF4</i>Deletions in Pitt-Hopkins Syndrome

    <i>TCF4</i>Deletions in Pitt-Hopkins Syndrome Dahkki Irina Giurgea, Chantal Missirian, Pierre Cacciagli, Sandra Whalen, Tessa Fredriksen, Thierry Gaillon, Julia Rankin, Michèle Mathieu‐Dramard, G Morin, Dominique Martin–Coignard, Christèle Dubourg, B. Chabrol, Jacqueline Arfi, Fabienne Giuliano, Jean Claude Lambert, Nicole Philip, Pierre Sarda, Laurent Villard, Michel Goossens, Anne Moncla

    Almmustuhtton 2008
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  9. 9
    Non-USH2A mutations in USH2 patients

    Non-USH2A mutations in USH2 patients Dahkki Thomas Besnard, Christel Vaché, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Sylvie Odent, Patricia Blanchet, Patrick Calvas, Christian Hamel, Hélène Dollfus, Geneviève Lina‐Granade, James Lespinasse, Albert David, Bertrand Isidor, G Morin, Sue Malcolm, Sylvie Tuffery‐Giraud, Mireille Claustres, Anne‐Françoise Roux

    Almmustuhtton 2011
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    Artigo
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  10. 10
    Treatment of two infants with PIK3CA-related overgrowth spectrum by alpelisib

    Treatment of two infants with PIK3CA-related overgrowth spectrum by alpelisib Dahkki G Morin, C. Degrugillier-Chopinet, Marie Vincent, Antoine Fraissenon, H. Aubert, Célia Chapelle, Clément Hoguin, François Dubos, B. Catteau, Florence Petit, Aurélie Mezel, Olivia Domanski, Guillaume Herbreteau, Marie Alesandrini, Nathalie Boddaert, Nathalie Boutry, Christine Broissand, Tianxiang Han, Fabrice Branle, Sabine Sarnacki, Thomas Blanc, Laurent Guibaud, Guillaume Canaud

    Almmustuhtton 2022
    Viečča ollesdeavstta
    Artigo
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  11. 11
    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome

    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome Dahkki Anne Debost‐Legrand, Cyrielle Tréard, Isabelle Roncelin, Sophie Dreux, Aurélia Bertholet‐Thomas, Françoise Broux, Bruno Daniele, Stéphane Decramer, Georges Deschênes, D. Djeddi, Vincent Guigonis, Nadine Jay, Tackwa Khalifeh, Brigitte Llanas, Denis Morin, G Morin, François Nobili, Christine Piétrement, Amélie Ryckewaert, Rémi Salomon, Isabelle Vrillon, Anne Blanchard, Rosa Vargas‐Poussou

    Almmustuhtton 2017
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    Artigo
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  12. 12
    COVID-19 in Patients on Maintenance Dialysis in the Paris Region

    COVID-19 in Patients on Maintenance Dialysis in the Paris Region Dahkki Sarah Tortonese, Ivan Scriabine, Louis Anjou, Christopher Loens, Arthur Michon, M. Benabdelhak, Sarah Ouali, G Morin, M. Laïfi, Hélène Dobosziewicz, Matthieu Guillet, Manon Dekeyser, Liem Binh Luong Nguyen, Anne Grünenwald, Julien Dang, Geoffroy Desbuissons, Laurent Becquemont, Renaud Snanoudj, Christophe Legendre, Hadia Hebibi, Édouard Lefèvre, Séverine Beaudreuil, Mohamad Zaidan

    Almmustuhtton 2020
    Viečča ollesdeavstta
    Artigo
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  13. 13
    Clinical and biological features in <i>PIEZO1</i>-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

    Clinical and biological features in <i>PIEZO1</i>-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients Dahkki Véronique Picard, Corinne Guitton, Isabelle Thuret, Christian Rosé, Laurence Bendélac, Khaldoun Ghazal, Patricia Aguilar‐Martinez, Catherine Badens, Claire Barro, Claire Bénéteau, Claire Berger, P. Cathébras, Éric Deconinck, Jacques Delaunay, J.M. Durand, Nadia Firah, Frédéric Galactéros, Bertrand Godeau, Xavier Jaïs, Jean-Pierre de Jaureguiberry, Camille Le Stradic, François Lifermann, Robert Maffre, G Morin, Julien Perrin, Valérie Proulle, M. Ruivard, Fabienne Toutain, Agnès Lahary, Loïc Garçon

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  14. 14
    Delineation of<i>EFTUD2</i>Haploinsufficiency-Related Phenotypes Through a Series of 36 Patients

    Delineation of<i>EFTUD2</i>Haploinsufficiency-Related Phenotypes Through a Series of 36 Patients Dahkki Daphné Lehalle, Christopher T. Gordon, Myriam Oufadem, Géraldine Goudefroye, Lucile Boutaud, Jean‐Luc Alessandri, Neus Baena, Geneviève Baujat, Clarisse Baumann, Odile Boute‐Bénéjean, Roseline Caumes, Christine Decaestecker, Dominique Gaillard, Alice Goldenberg, Marie Gonzalès, Muriel Holder‐Espinasse, Marie‐Line Jacquemont, Didier Lacombe, Sylvie Manouvrier‐Hanu, Sandrine Marlin, Michèle Mathieu‐Dramard, G Morin, Laurent Pasquier, Florence Petit, Marlène Rio, Robert Śmigiel, Christel Thauvin‐Robinet, Alexandre Vasiljevic, Alain Verloès, Valérie Malan, Arnold Münnich, Loïc de Pontual, Michel Vekemans, Stanislas Lyonnet, Tania Attié‐Bitach, Jeanne Amiel

    Almmustuhtton 2014
    Viečča ollesdeavstta
    Artigo
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  15. 15
    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

    A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling Dahkki Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, Sabine Steiner-Haldenstätt, Esther Pohl, Yun Li, Esther Milz, Marcel Martin, Holger Thiele, Janine Altmüller, Yasemin Alanay, Hülya Kayserili, Ludger Klein‐Hitpaß, Stefan Böhringer, Andreas Wollstein, Beate Albrecht, Koray Boduroğlu, Almuth Caliebe, Krystyńa Chrzańowska, Özgür Çoğulu, Francesca Cristofoli, Johanna Christina Czeschik, Koenraad Devriendt, Maria Teresa Dotti, Nursel Elçioğlu, Blanca Gener, Timm O. Goecke, Małgorzata Krajewska‐Walasek, Encarna Guillén‐Navarro, Joussef Hayek, Gunnar Houge, Esra KAYA KILIÇ, Pelin Özlem Şimşek‐Kiper, Vanesa López‐González, Alma Kuechler, Stanislas Lyonnet, Francesca Mari, Annabella Marozza, Michèle Mathieu Dramard, Barbara Mikat, G Morin, Fanny Morice‐Picard, Ferda Özkınay, Anita Rauch, Alessandra Renieri, Sigrid Tinschert, Gülen Eda Ütine, Catheline Vilain, Rossella Vivarelli, Christiane Zweier, Peter Nürnberg, Sven Rahmann, Joris Vermeesch, Hermann‐Josef Lüdecke, Michael Zeschnigk, Bernd Wollnik

    Almmustuhtton 2013
    Viečča ollesdeavstta
    Artigo
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  16. 16
    Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases

    Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases Dahkki Alain Verloès, Nataliya Di Donato, Julien Masliah‐Planchon, Marjolijn C.J. Jongmans, Omar A Abdul-Raman, Beate Albrecht, Judith Allanson, Han G. Brunner, Débora Romeo Bertola, Nicolas Chassaing, Albert David, Koenraad Devriendt, Pirayeh Eftekhari, Valérie Drouin‐Garraud, Francesca Faravelli, Laurence Faivre, Fabienne Giuliano, Leina Guion Almeida, Jorge L. Juncos, Marlies Kempers, Hatice Koçak Eker, Didier Lacombe, Angela E. Lin, Grazia M.S. Mancini, Daniela Melis, Charles Marques Lourenço, Victoria Mok Siu, G Morin, Marjan M. Nezarati, Małgorzata J.M. Nowaczyk, Jeanette C. Ramer, Sara Osimani, Nicole Philip, Mary Ella Pierpont, Vincent Procaccio, Zeichi-Seide Roseli, Massimiliano Rossi, Cristina Rusu, Yves Sznajer, Ludivine Templin, Vera Uliana, Mirjam Klaus, Bregje W.M. van Bon, Conny van Ravenswaaij, Bruce H. Wainer, Andrew E. Fry, Andreas Rump, Alexander Hoischen, Séverine Drunat, Jean‐Baptiste Rivière, William B. Dobyns, Daniela T. Pilz

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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