Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Jiangfeng, Mao"'
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare but life-threatening skin lesion triggered by hypersensitive drug reaction. They are characterized by extensive epidermal necrosis and skin exfoliation.
Externí odkaz:
https://doaj.org/article/cfed3c8204fd4cd9a61528dd4a50c53c
Autor:
Zhenxing Huang, Xi Wang, Bingqing Yu, Wanlu Ma, Pengyu Zhang, Xueyan Wu, Min Nie, Jiangfeng Mao
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 68 (2024)
ABSTRACT Objective: Both pulsatile gonadotropin-releasing hormone (GnRH) and combined gonadotropin therapy are effective to induce spermatogenesis in men with congenital hypogonadotropic hypogonadism (CHH). This study aimed to evaluate the effect of
Externí odkaz:
https://doaj.org/article/1dea04a78c13484ba78b765f942e57ab
Publikováno v:
BMC Gastroenterology, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Non-alcoholic fatty liver disease (NAFLD) is easily neglected in the non-obese population. TyG index (triglyceride glucose Index) and TG/HDL-c (triglyceride to high-density lipoprotein cholesterol) are new indicators to evaluate i
Externí odkaz:
https://doaj.org/article/29d63819bf654286ac82a928b9518eae
Publikováno v:
PLoS ONE, Vol 19, Iss 1 (2024)
Externí odkaz:
https://doaj.org/article/58151040374e4195a8344198ffd9a01e
Autor:
Xiaogang Li, Ye Guo, Xi Wang, Haolong Li, Jiangfeng Mao, Songxin Yan, Guoju Luo, Renzhi Wang, Xueyan Wu, Yongzhe Li
Publikováno v:
Heliyon, Vol 9, Iss 5, Pp e15657- (2023)
Externí odkaz:
https://doaj.org/article/a056fbb745b64334abd93c48f92005ec
Autor:
Xiaogang Li, Ye Guo, Xi Wang, Haolong Li, Jiangfeng Mao, Songxin Yan, Guoju Luo, Renzhi Wang, Xueyan Wu, Yongzhe Li
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e14779- (2023)
Background: Normosmic congenital hypogonadotropic hypogonadism (nCHH) is a rare disease, whose pathogenesis remains unclear. Here, we conducted untargeted metabolomics and lipidomics to identify seminal plasma signatures of nCHH, and to study the eff
Externí odkaz:
https://doaj.org/article/5a5f29dd4973409293469db2599bbb2e
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
BackgroundDecreasing mass and metabolism in skeletal muscle are associated with increasing insulin resistance (IR) and type 2 diabetes mellitus (T2DM). The causal relation between sarcopenia and abnormal glucose metabolism may be bidirectional. This
Externí odkaz:
https://doaj.org/article/495970a6741c44f099a1632caf6231ef
Autor:
Zhiyuan Zhao, Yinjie Gao, Lin Lu, Anli Tong, Shi Chen, Wei Zhang, Xiaoxia Zhang, Bang Sun, Xueyan Wu, Jiangfeng Mao, Xi Wang, Min Nie
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
ObjectiveTo analyze the relationship between genotype and phenotype in 21-Hydroxylase deficiency patients harboring P31L variant and the underlying mechanism.MethodsA total of 29 Chinese patients with 21-OHD harboring P31L variant were recruited, and
Externí odkaz:
https://doaj.org/article/0bd6c8a0c43e40d7ae5fbe47436131db
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Objective To identify the pathogenic mechanism of the c.244G>T mutation in NR5A1 gene found in a Chinese patient with 46, XY disorders of sex development (DSD). Subjects and methods: Genomic DNA was extracted from a Chinese 46, XY DSD patien
Externí odkaz:
https://doaj.org/article/5a3f470dfb314cdf80a5190c6f8e0d17
Autor:
Wen, Ji, Jiangfeng, Mao, Min, Nie, Xi, Wang, Shuying, Li, Bingqing, Yu, Rui, Zhang, Yinjie, Gao, Qibin, Huang, Xueyan, Wu
Publikováno v:
In Endocrine Practice February 2021 27(2):124-130