Zobrazeno 1 - 10 of 353 pro vyhledávání: '"gonadotropin-deficiency"'
1
Akademický článek
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3
Akademický článek
A case report supporting the concept that a role for the anti-Müllerian hormone (AMH) in normal folliculogenesis is to diminish the biological activity of follicle stimulating hormone (FSH)
Autor: J.H. Check, E. Chang, R. Cohen
Publikováno v: Clinical and Experimental Obstetrics & Gynecology, Vol 47, Iss 4, Pp 620-621 (2020)
Purpose: To describe a case where a woman was ovulating with regular menses despite very low sera follicle stimulating hormone (FSH) and luteinizing hormone (LH) levels. Case Report: Serum anti-Müllerian (AMH) was obtained because the woman was to b
Externí odkaz: https://doaj.org/article/f2d63df5218445569e66646d9324d0c5
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4
Akademický článek
Diagnosis and Treatment of Hypopituitarism
Autor: Seong Yeon Kim
Publikováno v: Endocrinology and Metabolism, Vol 30, Iss 4, Pp 443-455 (2015)
Hypopituitarism is a chronic endocrine illness that caused by varied etiologies. Clinical manifestations of hypopituitarism are variable, often insidious in onset and dependent on the degree and severity of hormone deficiency. However, it is associat
Externí odkaz: https://doaj.org/article/94d127e244ff4b368bf2162ea23fc3d8
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5
Akademický článek
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6
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty
Autor: Luigi Maione, Claire Bouvattier, Régis Coutant, Séverine Trabado, Aurelie Donzeau, Alejandra Cartes, Andrew A. Dwyer, Sylvie Brailly-Tabard, Gianpaolo De Filippo, Jacques Young, H. Mosbah, Philippe Chanson
Publikováno v: Human Reproduction. 35:2312-2322
STUDY QUESTION Are GnRH tests and serum inhibin B levels sufficiently discriminating to distinguish transient constitutional delay of growth and puberty (CDGP) from congenital hypogonadotropic hypogonadism (CHH) that affects reproductive health for l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18f5499bdde042d353f170a0aff6eec4
https://doi.org/10.1093/humrep/deaa185
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8
SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome
Autor: Akie Nakamura, Tsutomu Ogata, Mariko Nagamori, Maki Fukami, Erina Suzuki, Hirohito Shima, Satoshi Narumi, Yoko Izumi, Tomoko Jinno, Etsuro Tokuhiro, Shingo Okamoto
Publikováno v: Journal of the Endocrine Society
Introduction Kallmann syndrome (KS) is a genetically heterogeneous condition characterized by hypogonadotropic hypogonadism (HH) and olfactory dysfunction. Although SOX10, a causative gene for Waardenburg syndrome (WS) and peripheral demyelinating ne
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0883ec4975852e997bbcb3f853e26f68
http://europepmc.org/articles/PMC8170842
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9
A survey of surgically resected pituitary incidentalomas and a comparison of the clinical features and surgical outcomes of non-functioning pituitary adenomas discovered incidentally versus symptomatically
Autor: Akio Morita, Akimi Soga, Mayo Ono, Izumi Fukuda, Shigeyuki Tahara, Hitoshi Sugihara
Publikováno v: Endocrine journal. 68(5)
Pituitary tumors are discovered either incidentally by imaging studies (incidentalomas) or via evaluation of certain clinical symptoms (symptomatic tumors). In this study, we first surveyed patients with incidentalomas who underwent surgery. Cases in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927e4428892daa242732dbc837357e2c
https://pubmed.ncbi.nlm.nih.gov/33504715
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10
Neuroendocrine manifestations of Langerhans cell histiocytosis
Autor: Gregory Kaltsas, Marina Tsoli, Maria P. Yavropoulou
Publikováno v: The Human Hypothalamus-Neuroendocrine Disorders ISBN: 9780128206836
Langerhans cell histiocytosis (LCH) is a rare inflammatory myeloid neoplasia that can affect any organ or system in the human body. It is usually diagnosed during childhood but can also affect adults. Recent studies have demonstrated involvement of t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::50e2a982c8af48aaf107395ad32949ea
https://doi.org/10.1016/b978-0-12-820683-6.00009-9
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