檢索結果 - Céline Huot
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Severe Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in an Adolescent Girl with a Novel<i>AIRE</i>Mutation: Response to Immunosuppressive Therapy<sup>1</sup> 由 Leanne M. Ward, Jean Paquette, Ernest G. Seidman, Céline Huot, Fernando Alvarez, Patricia Crock, Edgar Delvin, Olle Kämpe, Cheri Deal
出版 1999Artigo -
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A Novel Mechanism for Isolated Central Hypothyroidism: Inactivating Mutations in the Thyrotropin-Releasing Hormone Receptor Gene<sup>1</sup> 由 R. Collu, JangQing Tang, Jérôme Castagné, Ginette Lagacé, Nicole Masson, Céline Huot, Cheri Deal, Edgard Delvin, Elena Faccenda, Karin A. Eidne, Guy Van Vliet
出版 1997Artigo -
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Bioinactive ACTH Causing Glucocorticoid Deficiency 由 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
出版 2013Artigo -
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Mutations in<i>Prokineticin 2</i>and<i>Prokineticin receptor 2</i>genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum 由 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
出版 2008Artigo -
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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice 由 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
出版 2008Artigo
相關主題
Endocrinology
Medicine
Internal medicine
Biology
Gene
Genetics
Mutation
Compound heterozygosity
Hormone
Coronavirus disease 2019 (COVID-19)
Diabetes management
Diabetes mellitus
Diabetic ketoacidosis
Disease
Infectious disease (medical specialty)
Intensive care medicine
Kallmann syndrome
Missense mutation
Mutant
Pediatrics
Proband
Psychiatry
Psychosocial
Receptor
Type 1 diabetes
Type 2 diabetes
ACTH receptor
Adipocyte
Adipose tissue
Adrenal insufficiency