Torthaí cuardaigh - Elka Jacobson-Dickman

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  1. 1
    Vitamin D Supplementation and Risk of Toxicity in Pediatrics: A Review of Current Literature

    Vitamin D Supplementation and Risk of Toxicity in Pediatrics: A Review of Current Literature de réir Maria G. Vogiatzi, Elka Jacobson-Dickman, Mark D. DeBoer

    Foilsithe / Cruthaithe 2014
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  2. 2
    Endocrine Effects of Inhaled Corticosteroids in Children

    Endocrine Effects of Inhaled Corticosteroids in Children de réir Chirag Kapadia, Todd D. Nebesio, S Myers, Steven M. Willi, Bradley S. Miller, David B. Allen, Elka Jacobson-Dickman

    Foilsithe / Cruthaithe 2015
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  3. 3
    Loss-of-function mutation in the <i>prokineticin 2</i> gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

    Loss-of-function mutation in the <i>prokineticin 2</i> gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism de réir Nelly Pitteloud, Chengkang Zhang, Duarte Pignatelli, Jia‐Da Li, Taneli Raivio, Lindsay W. Cole, Lacey Plummer, Elka Jacobson-Dickman, Pamela L. Mellon, Qun‐Yong Zhou, William F. Crowley

    Foilsithe / Cruthaithe 2007
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    Artigo
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  4. 4
    Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

    Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism de réir Taneli Raivio, Yisrael Sidis, Lacey Plummer, Huaibin Chen, Jinghong Ma, Abir Mukherjee, Elka Jacobson-Dickman, Richard Quinton, Guy Van Vliet, Hélène B. Lavoie, Virginia Hughes, Andrew Dwyer, Frances J. Hayes, Shuyun Xu, Susan Sparks, Ursula B. Kaiser, Moosa Mohammadi, Nelly Pitteloud

    Foilsithe / Cruthaithe 2009
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  5. 5
    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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  6. 6
    An ancient founder mutation in PROKR2 impairs human reproduction

    An ancient founder mutation in PROKR2 impairs human reproduction de réir Magdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P. Sykiotis, Jacques Young, Richard Quinton, Ana Paula Abreu, Lacey Plummer, Margaret Au, Ravikumar Balasubramanian, Andrew Dwyer, José C. Florez, Timothy Cheetham, Simon H. S. Pearce, Radhika Purushothaman, Albert Schinzel, Michel Pugeat, Elka Jacobson-Dickman, Svetlana Ten, Ana Cláudia Latronico, James F. Gusella, Catherine Dodé, William F. Crowley, Nelly Pitteloud

    Foilsithe / Cruthaithe 2012
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  7. 7
    Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations

    Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations de réir Carine Villanueva, Elka Jacobson-Dickman, Cheng Xu, Sylvie Manouvrier, Andrew Dwyer, Gerasimos P. Sykiotis, Andrew Beenken, Yang Liu, Johanna Tommiska, Youli Hu, Dov Tiosano, Marion Gérard, Juliane Léger, Valérie Drouin‐Garraud, Hervé Lefèbvre, Michel Polak, Jean‐Claude Carel, Franziska Phan-Hug, Michael Hauschild, Lacey Plummer, Jean-Pierre Rey, Taneli Raivio, Pierre Bouloux, Yisrael Sidis, Moosa Mohammadi, Nicolás de Roux, Nelly Pitteloud

    Foilsithe / Cruthaithe 2014
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