Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Wen-mu Hu"'
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
ObjectiveChronic hypercortisolism leads to a phenotype resembling metabolic syndrome. We aimed to investigate the association between gut microbiota and metabolic abnormalities in endogenous hypercortisolism (Cushing’s syndrome).MethodsA total of 2
Externí odkaz:
https://doaj.org/article/7c20915d0d084d8d93d716b15fee2fb0
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Objective: Congenital lipid adrenal hyperplasia (LCAH) is the most serious type of congenital adrenal hyperplasia and is caused by steroid-based acute regulatory (STAR) protein mutations. Herein, we report compound heterozygous mutations c.558C>A (p.
Externí odkaz:
https://doaj.org/article/07a4cc8dd5654d3e848f082e3c6da7b0
Background: 48, XXYY Klinefelter syndrome is a rare sex chromosome abnormality. Nonsyndromic hearing loss (NSHL) is the most frequent hereditary type of hearing impairment. There has been no report of NSHL combined with 48XXYY. The purpose of this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00d2772f8065c91c3974fa23461d9e78
https://doi.org/10.21203/rs.3.rs-92862/v1
https://doi.org/10.21203/rs.3.rs-92862/v1
Autor:
Xuefei Xiao, Sheng ping Liu, Wen mu Hu, Chun Liu, Min Zhang, Qin Zhang, Zongdao Liu, Ping Jin, Wei Wang
Publikováno v:
Diabetes Research and Clinical Practice
Aims The objective of this study is to explore the association between documented diabetes, fasting plasma glucose (FPG), and the clinical outcomes of Coronavirus disease 2019 (COVID-19) . Methods This retrospective study included 255 patients with C