Yanning Song
Overview
Explore the profile of Yanning Song including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
236
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Recent Articles
1.
Liu M, Cao B, Luo Q, Song Y, Liu K, Wu D
Front Endocrinol (Lausanne)
. 2025 Jan;
15():1474384.
PMID: 39845880
Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) has become one of the most prevalent chronic liver diseases worldwide. The serum uric acid-to-high-density lipoprotein cholesterol ratio (UHR) has been recognized as...
2.
Yuan Z, Fan L, Wang Y, Li L, Ren X, Sui S, et al.
Eur J Endocrinol
. 2024 Jun;
191(1):87-96.
PMID: 38938059
Context: Androgen insensitivity syndrome (AIS) manifests itself as variable symptoms of under-virilization in patients with 46,XY disorders caused by androgen receptor (AR) gene variants. This large-sample study aimed to correlate...
3.
Liu M, Cao B, Luo Q, Song Y, Shi Y, Cheng M, et al.
Diabetes Metab Syndr Obes
. 2024 Jan;
17:381-391.
PMID: 38283639
Objective: To explore the gender-, age-, and weight status-specific prevalence of hyperuricemia (HUA) and its associated risk factors among Chinese children and adolescents with obesity. Methods: A total of 1329...
4.
Deng H, He L, Wang C, Zhang T, Guo H, Zhang H, et al.
BMC Psychiatry
. 2022 Sep;
22(1):629.
PMID: 36167540
Background: The pathophysiological mechanisms of aggression are manifold and they may closely interconnect. Current study aimed to determine the gut microbiota and its metabolites, and clarify their correlations with inflammation,...
5.
Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study
Zhao X, Su Z, Chen S, Wang X, Yang Y, Chen L, et al.
J Pers Med
. 2022 May;
12(5).
PMID: 35629193
Objective: To provide new information about androgen insensitivity syndrome (AIS), we studied growth patterns in Chinese children with AIS. Subjects: Data are from 118 untreated AIS patients who were admitted...
6.
Wang Y, Fan L, Ren X, Song Y, Zhang B, Gong C
Chin Med J (Engl)
. 2021 Nov;
135(4):477-479.
PMID: 34759222
No abstract available.
7.
Yu C, Xie B, Zhao Z, Zhao S, Liu L, Cheng X, et al.
Front Endocrinol (Lausanne)
. 2021 Sep;
12:711991.
PMID: 34589056
Purpose: Congenital growth hormone deficiency (GHD) is a rare and etiologically heterogeneous disease. We aim to screen disease-causing mutations of GHD in a relatively sizable cohort and discover underlying mechanisms...
8.
Fan X, Zhao S, Yu C, Wu D, Yan Z, Fan L, et al.
J Genet Genomics
. 2021 May;
48(5):396-402.
PMID: 34006472
Short stature is among the most common endocrinological disease phenotypes of childhood and may occur as an isolated finding or in conjunction with other clinical manifestations. Although the diagnostic utility...
9.
Gui B, Yu C, Li X, Zhao S, Zhao H, Yan Z, et al.
Front Cell Dev Biol
. 2021 May;
9:661747.
PMID: 33937263
Purpose: ROR2, a member of the ROR family, is essential for skeletal development as a receptor of Wnt5a. The present study aims to investigate the mutational spectrum of in children...
10.
Shi L, Huang H, Lu X, Yan X, Jiang X, Xu R, et al.
Signal Transduct Target Ther
. 2021 Feb;
6(1):58.
PMID: 33568628
Treatment of severe Coronavirus Disease 2019 (COVID-19) is challenging. We performed a phase 2 trial to assess the efficacy and safety of human umbilical cord-mesenchymal stem cells (UC-MSCs) to treat...