Zobrazeno 1 - 10
of 815
pro vyhledávání: '"hypogonadotrophic hypogonadism"'
Autor:
Yuri Aung, Vasilis Kokotsis, Kyla Ng Yin, Kausik Banerjee, Gary Butler, Mehul T. Dattani, Paul Dimitri, Leo Dunkel, Claire Hughes, Michael McGuigan, Márta Korbonits, George Paltoglou, Sophia Sakka, Pratik Shah, Helen L. Storr, Ruben H. Willemsen, Sasha R. Howard
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionDelayed puberty (DP) is a frequent concern for adolescents. The most common underlying aetiology is self-limited DP (SLDP). However, this can be difficult to differentiate from the more severe condition congenital hypogonadotrophic hypogo
Externí odkaz:
https://doaj.org/article/88afa92d063948b29fdf6c6b1467cf4f
Autor:
Ali Abbara, Kanyada Koysombat, Maria Phylactou, Pei Chia Eng, Sophie Clarke, Alexander N. Comninos, Lisa Yang, Chioma Izzi-Engbeaya, Simon Hanassab, Neil Smith, Channa N. Jayasena, Cheng Xu, Richard Quinton, Nelly Pitteloud, Gerhard Binder, Ravinder Anand-Ivell, Richard Ivell, Waljit S. Dhillo
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundDelayed puberty in males is almost invariably associated with constitutional delay of growth and puberty (CDGP) or congenital hypogonadotrophic hypogonadism (CHH). Establishing the cause at presentation is challenging, with “red flag” f
Externí odkaz:
https://doaj.org/article/65865504228c43389686a6059514ae8a
Autor:
Kalhan, Atul, editor
Publikováno v:
Best of Five MCQs for the Endocrinology and Diabetes SCE, 2022.
Externí odkaz:
https://doi.org/10.1093/oso/9780198864615.003.0005
Autor:
Jordan Teoli, Vincent Mezzarobba, Lucie Renault, Delphine Mallet, Hervé Lejeune, Pierre Chatelain, Frédérique Tixier, Marc Nicolino, Noël Peretti, Sandrine Giscard D’estaing, Béatrice Cuzin, Frédérique Dijoud, Florence Roucher-Boulez, Ingrid Plotton
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundNR0B1 pathogenic variants can cause congenital adrenal hypoplasia or primary adrenal insufficiency in early childhood usually associated with hypogonadotropic hypogonadism. NR0B1 is necessary for organogenesis of the adrenal cortex and to m
Externí odkaz:
https://doaj.org/article/ef86f28659bf4fe2a50c23e556146cd3
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
SOX3 is critical for the development of the pituitary, brain, and face, and SOX3 mutations may lead to hypopituitarism, intellectual disability, and craniofacial abnormalities. Common SOX3 mutations are duplications and deletions of the whole or part
Externí odkaz:
https://doaj.org/article/e8382e4f77a54e2ba6bb925c3d618259
Publikováno v:
JCRPE, Vol 11, Iss 4, Pp 444-448 (2019)
Idiopathic hypogonadotropic hypogonadism (IHH) is a rare disease caused by defects in the secretion of gonadotropin releasing hormone (GnRH) or the action of GnRH on the pituitary gonadotrophes. KISS1R is one of the genes which, when mutated, cause I
Externí odkaz:
https://doaj.org/article/be543b9116724df3ad213f3bc9919847
Autor:
Agnieszka Pazderska, Yaasir Mamoojee, Satish Artham, Margaret Miller, Stephen G Ball, Tim Cheetham, Richard Quinton
Publikováno v:
Endocrine Connections, Vol 7, Iss 1, Pp 133-138 (2018)
We present herein our 20-year experience of pubertal induction in apubertal older (median age 56 years; range 38.4–69.5) men with congenital hypogonadotrophic hypogonadism (n = 7) using a simple fixed-dose and fixed-interval intramuscular testoster
Externí odkaz:
https://doaj.org/article/c382b1b189d546e3b2d090bfe0301b91
Autor:
Agnieszka Lecka-Ambroziak, Marta Wysocka-Mincewicz, Kamila Marszałek-Dziuba, Agnieszka Rudzka-Kocjan, Mieczysław Szalecki
Publikováno v:
Life, Vol 10, Iss 10, p 237 (2020)
Puberty in children with Prader-Willi syndrome (PWS) is usually delayed and/or incomplete but in some patients premature/early adrenarche is observed. We assessed the premature adrenarche (PA) in PWS patients during the recombinant human growth hormo
Externí odkaz:
https://doaj.org/article/a981bc168b424010956671fe808f5cea
Autor:
Dilinie Herbert, Rakibul M. Islam, Robin J. Bell, Susan R. Davis, Marina A Skiba, Alejandra Martinez Garcia
Publikováno v:
Human Reproduction. 37:109-118
STUDY QUESTION Can serum anti-Müllerian hormone (AMH) replace polycystic ovary morphology (PCOM) determined by ultrasound as a diagnostic component of polycystic ovary syndrome (PCOS)? SUMMARY ANSWER Despite good correlations between serum AMH and P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d267a85be397fae23b7eb4e7f643aca
https://doi.org/10.1093/humrep/deab232
https://doi.org/10.1093/humrep/deab232
Publikováno v:
INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine). 15:402-409
Oгляд сфокусований на діагностиці, клінічному і загальному терапевтичному підході до конституціональної затримки росту та статевого д
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e54b7b9c93cfc0859459a07a912fbe2d
https://doi.org/10.22141/2224-0721.15.5.2019.180045
https://doi.org/10.22141/2224-0721.15.5.2019.180045