Torthaí cuardaigh - Céline Huot

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  1. 1
    Type 1 Diabetes in Children and Adolescents

    Type 1 Diabetes in Children and Adolescents de réir Diane K. Wherrett, Céline Huot, Beth D. Mitchell, Danièle Pacaud

    Foilsithe / Cruthaithe 2013
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    Artigo
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  2. 2
    Type 1 Diabetes in Children and Adolescents

    Type 1 Diabetes in Children and Adolescents de réir Diane K. Wherrett, Josephine Ho, Céline Huot, Laurent Legault, Meranda Nakhla, Elizabeth Rosolowsky

    Foilsithe / Cruthaithe 2018
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    Artigo
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  3. 3
    Elevated Serum 25(OH)D Concentrations, Vitamin D, and Calcium Intakes Are Associated With Reduced Adipocyte Size in Women

    Elevated Serum 25(OH)D Concentrations, Vitamin D, and Calcium Intakes Are Associated With Reduced Adipocyte Size in Women de réir Maude Caron‐Jobin, Anne‐Sophie Morisset, Angelo Tremblay, Céline Huot, Denis Légaré, André Tchernof

    Foilsithe / Cruthaithe 2011
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    Artigo
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  4. 4
    Severe Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in an Adolescent Girl with a Novel<i>AIRE</i>Mutation: Response to Immunosuppressive Therapy<sup>1</sup>

    Severe Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in an Adolescent Girl with a Novel<i>AIRE</i>Mutation: Response to Immunosuppressive Therapy<sup>1</sup> de réir Leanne M. Ward, Jean Paquette, Ernest G. Seidman, Céline Huot, Fernando Alvarez, Patricia Crock, Edgar Delvin, Olle Kämpe, Cheri Deal

    Foilsithe / Cruthaithe 1999
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  5. 5
    A Novel Mechanism for Isolated Central Hypothyroidism: Inactivating Mutations in the Thyrotropin-Releasing Hormone Receptor Gene<sup>1</sup>

    A Novel Mechanism for Isolated Central Hypothyroidism: Inactivating Mutations in the Thyrotropin-Releasing Hormone Receptor Gene<sup>1</sup> de réir R. Collu, JangQing Tang, Jérôme Castagné, Ginette Lagacé, Nicole Masson, Céline Huot, Cheri Deal, Edgard Delvin, Elena Faccenda, Karin A. Eidne, Guy Van Vliet

    Foilsithe / Cruthaithe 1997
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  6. 6
    Bioinactive ACTH Causing Glucocorticoid Deficiency

    Bioinactive ACTH Causing Glucocorticoid Deficiency de réir Mark E. Samuels, Nicole Gallo‐Payet, Sandra Pinard, Caroline Hasselmann, Fabien Magne, Lysanne Patry, L. A. Chouinard, Jeremy Schwartzentruber, Patricia René, Nicole Sawyer, Michel Bouvier, Anissa Djemli, Edgard Delvin, Céline Huot, Dardye Eugène, Cheri Deal, Guy Van Vliet, Jacek Majewski, Johnny Deladoëy

    Foilsithe / Cruthaithe 2013
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  7. 7
    Mutations in<i>Prokineticin 2</i>and<i>Prokineticin receptor 2</i>genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

    Mutations in<i>Prokineticin 2</i>and<i>Prokineticin receptor 2</i>genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum de réir Lindsay W. Cole, Yisrael Sidis, Chengkang Zhang, Richard Quinton, Lacey Plummer, Duarte Pignatelli, Virginia Hughes, Andrew Dwyer, Taneli Raivio, Frances J. Hayes, Stephanie B. Seminara, Céline Huot, Nathalie Alos, Phyllis Speiser, Akira Takeshita, Guy VanVliet, Simon H. S. Pearce, William F. Crowley, Qun‐Yong Zhou, Nelly Pitteloud

    Foilsithe / Cruthaithe 2008
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  8. 8
    Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

    Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice de réir John Falardeau, W. C. Chung, Andrew Beenken, Taneli Raivio, Lacey Plummer, Yisrael Sidis, Elka Jacobson-Dickman, Anna V. Eliseenkova, Jinghong Ma, Andrew Dwyer, Richard Quinton, Sandra Na, Janet E. Hall, Céline Huot, Natalie Alois, Simon H. S. Pearce, Lindsay W. Cole, Virginia Hughes, Moosa Mohammadi, Pei‐San Tsai, Nelly Pitteloud

    Foilsithe / Cruthaithe 2008
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