Zobrazeno 1 - 10
of 2 946
pro vyhledávání: '"delayed puberty"'
Not just a tragic compromise: The positive case for adolescent access to puberty‐blocking treatment.
Autor:
Wenner, Danielle M.1 danielle.wenner@gmail.com, George, B. R.1
Publikováno v:
Bioethics. Nov2021, Vol. 35 Issue 9, p925-931. 7p.
Autor:
Shimaa Medhat Abdellatif Ahmed, Nora ElSaid Badawi, Mohamed Ahmed AbdElSalam, Lubna Fawaz, AbdelKarim Kamel, Mona Mamdouh Hassan
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-8 (2024)
Abstract Background Differentiation between isolated hypogonadotropic hypogonadism (IHH) and constitutional delay in puberty (CDP) throughout adolescence can be challenging for doctors. This study examines the withdrawal effects of short-term, low-do
Externí odkaz:
https://doaj.org/article/63492508c83a470ca34a244dbb2adbbd
Autor:
Calvillo-Romero, Yeni, Galicia-Juárez, Eunice, Acosta-Altamirano, Gustavo, Valencia-Ledezma, Omar E., Castro-Fuentes, Carlos A.
Publikováno v:
Revista Mexicana de Endocrinología, Metabolismo y Nutrición; jul-sep2024, Vol. 11 Issue 3, p106-111, 6p
Autor:
Williams, Cara E.
Publikováno v:
Obstetrics, Gynaecology & Reproductive Medicine; Jun2024, Vol. 34 Issue 6, p147-152, 6p
Publikováno v:
Reproductive Health of Woman; 2024, Vol. 72 Issue 5, p8-12, 5p
Autor:
Azlansyah Azlansyah, Cennikon Pakpahan, Hermansyah Hermansyah, Faisal Yusuf Ashari, Gustavo Santos Rainato, Kenley Nathanael, Maxwell Salvador Surya Atmaja
Publikováno v:
Biomolecular and Health Science Journal, Vol 7, Iss 1, Pp 75-79 (2024)
Kallmann syndrome is defined as the association of hypogonadotropic hypogonadism and anosmia or hyposmia caused by abnormal migration of olfactory axons and neurons producing gonadotropin-releasing hormone. It is a nonlife-threatening disease with re
Externí odkaz:
https://doaj.org/article/2ab8cdd97ff9449c85f9dcb4d1a5b920
Autor:
Yeni Calvillo-Romero, Eunice Galicia-Juárez, Gustavo Acosta-Altamirano, Omar E. Valencia-Ledezma, Carlos A. Castro-Fuentes
Publikováno v:
Revista Mexicana de Endocrinología, Metabolismo y Nutrición, Vol 11, Iss 3 (2024)
Kallmann syndrome is a low-frequency pathology that mainly affects men. This case report aims to present the management of a pediatric patient diagnosed with Kallmann syndrome in Mexico. An 11-year-old male patient presented with a micropenis, crypto
Externí odkaz:
https://doaj.org/article/6fe0f372e39e4bdab374add84587ad59
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Key Clinical Message Among the total 10 reported cases with 20p13 microdeletion, including our patient, it is notable that 50% of patients presented a height below the 3rd percentile. We suggest that short stature is among the most common manifestati
Externí odkaz:
https://doaj.org/article/62fc64427a96470d88aa1581b8940b26
Autor:
Bozzola, Mauro1,2 mauro.bozzola@unipv.it, Bozzola, Elena3, Montalbano, Chiara1,2, Stamati, Filomena Andreina4, Ferrara, Pietro5, Villani, Alberto3
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism. Jun2018, Vol. 23 Issue 2, p58-61. 4p.
Autor:
Loscalzo, Emely, See, Julia, Bharill, Sonum, Yousefzadeh, Nazanin, Gough, Ethan, Wu, Malinda, Crane, Janet L.
Publikováno v:
Osteoporosis International; Feb2024, Vol. 35 Issue 2, p327-338, 12p