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European Journal of Endocrinology|August 7, 2017
Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutationsMin Nie, Hongli Xu, Rongrong Chen, et al.
Steroids|August 5, 2017
Novel mutations of HSD17B3 in three Chinese patients with 46,XY Disorders of Sex DevelopmentBingqing Yu, Zhaoxiang Liu, Jiangfeng Mao, et al.
Virulence|December 28, 2024
Arginine depletion-induced autophagy and metabolic dysregulation are involved in the disease severity of hand, foot, and mouth diseaseYuefei Jin, Wangquan Ji, Liang Zhang, et al.
Frontiers in Endocrinology|October 3, 2022
The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadismBingqing Yu, Kepu Chen, Jiangfeng Mao, et al.
Endocrine|September 25, 2023
Mixed hypogonadism: a neglected combined form of hypogonadismRui Zhang, Bingqing Yu, Xi Wang, et al.
Clinical Endocrinology|January 6, 2025
Body Composition, Adipocytokine, and Metabolic Parameters in Men With Congenital Hypogonadotropic HypogonadismRui Zhang, Jiangfeng Mao, Min Nie, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|April 29, 2021
Gonadotropin Therapy Once a Week for Spermatogenesis in Hypogonadotropic HypogonadismWanlu Ma, Jiangfeng Mao, Min Nie, et al.
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