Zobrazeno 1 - 10
of 3 073
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:
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:
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
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
Publikováno v:
Indian Journal of Physiotherapy & Occupational Therapy; 2024 Special Issue, Vol. 18, p832-837, 6p
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:
Aurora Lanzafame, Giorgia Pepe, Roberto Coco, Fabio Toscano, Mariella Valenzise, Malgorzata Wasniewska
Publikováno v:
Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche, Vol 111, Iss 2, Pp 1-5 (2023)
Pituitary stalk interruption syndrome (PSIS) is a rare congenital abnormality affecting thehypothalamic pituitary complex. It is characterized by a peculiar radiological triad which includes thin or interruptedpituitary stalk, hypoplasia or aplasia o
Externí odkaz:
https://doaj.org/article/7afdb878239548b881af6580b5a3e127
Autor:
Qingqing Tian, Jingjing Tang, Lihong Wang, Jiaojiao Liu, Xiangshan Li, Zhuozhuo Cao, Zhufang Tian
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Idiopathic hypogonadotropic hypogonadism (IHH) is a rare congenital or acquired genetic disorder caused by gonadotropin-releasing hormone (GnRH) deficiency. IHH patients are divided into two major groups, hyposmic or anosmic IHH (
Externí odkaz:
https://doaj.org/article/72d88f1978314814a21e682e8277b283