Cargando…
Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations
OBJECTIVE: The aim of this study was to investigate the clinical characteristics of patients diagnosed with congenital hypogonadotropic hypogonadism (CHH) caused by FGFR1 (fibroblast growth factor receptor 1) gene mutations and to evaluate the effect of gonadotropin or pulsatile gonadotropin-releasi...
Autores principales: | Li, Shuying, Zhao, Yaling, Nie, Min, Ma, Wanlu, Wang, Xi, Ji, Wen, Yang, Yufan, Hao, Ming, Yu, Bingqing, Gao, Yinjie, Mao, Jiangfeng, Wu, Xueyan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737440/ https://www.ncbi.nlm.nih.gov/pubmed/33354214 http://dx.doi.org/10.1155/2020/8873532 |
Ejemplares similares
-
Optimal treatment for spermatogenesis in male patients with hypogonadotropic hypogonadism
por: Lin, Jianli, et al.
Publicado: (2019) -
Assisted reproductive techniques with congenital hypogonadotropic hypogonadism patients: a systematic review and meta-analysis
por: Gao, Yinjie, et al.
Publicado: (2018) -
The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadism
por: Yu, Bingqing, et al.
Publicado: (2022) -
Classification of CHD7 Rare Variants in Chinese Congenital Hypogonadotropic Hypogonadism Patients and Analysis of Their Clinical Characteristics
por: Sun, Bang, et al.
Publicado: (2022) -
Induction of spermatogenesis in men with hypogonadotropic hypogonadism
por: Morris, Guy C., et al.
Publicado: (2021)