Výsledky vyhledávání - Virginia Hughes
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Microglia: The constant gardeners Autor Virginia Hughes
Vydáno 2012Artigo -
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Epigenetics: The sins of the father Autor Virginia Hughes
Vydáno 2014Artigo -
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Sarcopenia: Current Concepts Autor Ronenn Roubenoff, Virginia Hughes
Vydáno 2000Revisão -
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Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications Autor Hilana Lewkowitz-Shpuntoff, Virginia Hughes, Lacey Plummer, Margaret Au, Richard L. Doty, Stephanie B. Seminara, Yee-Ming Chan, Nelly Pitteloud, William F. Crowley, Ravikumar Balasubramanian
Vydáno 2011Artigo -
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Reversal of Idiopathic Hypogonadotropic Hypogonadism Autor Taneli Raivio, John Falardeau, Andrew Dwyer, Richard Quinton, Frances J. Hayes, Virginia Hughes, Lindsay W. Cole, Simon H. S. Pearce, Hang Lee, Paul A. Boepple, William F. Crowley, Nelly Pitteloud
Vydáno 2007Artigo -
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Oligogenic basis of isolated gonadotropin-releasing hormone deficiency Autor Gerasimos P. Sykiotis, Lacey Plummer, Virginia Hughes, Margaret Au, Sadia Durrani, Sadhana Nayak-Young, Andrew Dwyer, Richard Quinton, Janet E. Hall, James F. Gusella, Stephanie B. Seminara, William F. Crowley, Nelly Pitteloud
Vydáno 2010Artigo -
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Expanding the Phenotype and Genotype of Female GnRH Deficiency Autor Natalie D. Shaw, Stephanie B. Seminara, Corrine K. Welt, Margaret Au, Lacey Plummer, Virginia Hughes, Andrew Dwyer, Kathryn A. Martin, Richard Quinton, Verónica Mericq, Paulina M. Merino, James F. Gusella, William F. Crowley, Nelly Pitteloud, Janet E. Hall
Vydáno 2011Artigo -
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Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism Autor Nelly Pitteloud, James S. Acierno, Astrid U. Meysing, Anna V. Eliseenkova, Jinghong Ma, Omar A. Ibrahimi, Daniel L. Metzger, Frances J. Hayes, Andrew Dwyer, Virginia Hughes, Maria A. Yialamas, Janet E. Hall, Ellen C. G. Grant, Moosa Mohammadi, William F. Crowley
Vydáno 2006Artigo -
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Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism Autor 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
Vydáno 2009Artigo -
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<i>Heparan sulfate 6-O-sulfotransferase 1</i> , a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism Autor Janne Tornberg, Gerasimos P. Sykiotis, Kimberly W. Keefe, Lacey Plummer, Xuan Lan Thi Hoang, Janet E. Hall, Richard Quinton, Stephanie B Seminara, Virginia Hughes, Guy Van Vliet, Stan Van Uum, William F. Crowley, Hiroko Habuchi, Koji Kimata, Nelly Pitteloud, Hannes E. Bülow
Vydáno 2011Artigo -
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A Genetic Basis for Functional Hypothalamic Amenorrhea Autor Lisa M. Caronia, Cecilia Martin, Corrine K. Welt, Gerasimos P. Sykiotis, Richard Quinton, Apisadaporn Thambundit, Magdalena Avbelj Stefanija, Sadhana Dhruvakumar, Lacey Plummer, Virginia Hughes, Stephanie B. Seminara, Paul A. Boepple, Yisrael Sidis, William F. Crowley, Kathryn A. Martin, Janet E. Hall, Nelly Pitteloud
Vydáno 2011Artigo -
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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 Autor 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
Vydáno 2008Artigo -
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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice Autor 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
Vydáno 2008Artigo -
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Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism Autor Nelly Pitteloud, Richard Quinton, Simon H. S. Pearce, Taneli Raivio, James S. Acierno, Andrew Dwyer, Lacey Plummer, Virginia Hughes, Stephanie B. Seminara, Yuzhu Cheng, Weiping Li, Gavin MacColl, Anna V. Eliseenkova, Shaun K. Olsen, Omar A. Ibrahimi, Frances J. Hayes, Paul A. Boepple, Janet E. Hall, Pierre Bouloux, Moosa Mohammadi, William F. Crowley
Vydáno 2007Artigo
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Biology
Endocrinology
Genetics
Disease
Gene
Hormone
Hypogonadotropic hypogonadism
Coronavirus disease 2019 (COVID-19)
Infectious disease (medical specialty)
Kallmann syndrome
Mutation
Proband
Anosmia
Phenotype
Physical medicine and rehabilitation
Receptor
Fibroblast growth factor
Genotype
Kisspeptin
Luteinizing hormone
Muscle strength
Anatomy
Body mass index
Body weight
Cell biology
Context (archaeology)
Delayed puberty
Elbow