Chun-Xiu Gong
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Explore the profile of Chun-Xiu Gong including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
180
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Recent Articles
1.
Zhao M, Feng G, Cao B, Zheng Y, Gong C
J Pediatr Endocrinol Metab
. 2025 Jan;
38(3):254-261.
PMID: 39815165
Objectives: To develop a clinical model for predicting the occurrence of Central Precocious Puberty based on the breast development outcomes in chinese girls. Methods: This is a retrospective study, which...
2.
Wang Q, Liu M, Cao B, Su C, Meng X, Ding Y, et al.
Am J Med Genet A
. 2025 Jan;
e63987.
PMID: 39780405
Pediatric patients of autosomal dominant early onset osteoporosis conferred by heterozygous mutation in the WNT1 (OMIM: 615221) were rarely reported, and therapy in pediatrics is relatively inexperienced. The clinical and...
3.
Li Y, Yan M, Song Y, Zhang Q, Gong C
Endocrine
. 2025 Jan;
PMID: 39762666
Purpose: This study aimed to determine the detection rate of autoimmune polyendocrine syndrome (APS) among children with Graves' disease (GD) at a single center and to compare clinical characteristics between...
4.
Li Y, Wang X, Shi W, Chen J, Song Y, Gong C
Clin Endocrinol (Oxf)
. 2024 Nov;
102(2):196-204.
PMID: 39501471
Background: Antithyroid drugs (ATDs) are the preferred treatment option for Graves' disease (GD), yet there is a lack of systematic evaluations studying the relationship between treatment duration and therapeutic outcomes....
5.
Liu P, Li Z, Song H, Gong C, Zhang W
Asian J Androl
. 2024 Aug;
26(6):617-621.
PMID: 39119665
Central precocious puberty secondary to Leydig cell tumors is rare in children. We retrospectively analyzed the mid- to long-term follow-up data of patients with Leydig cell tumors. The clinical data...
6.
Wang Q, Chen J, Wei L, Ding Y, Liu M, Li W, et al.
Orphanet J Rare Dis
. 2024 Mar;
19(1):126.
PMID: 38504242
Objective: Idiopathic infantile hypercalcemia (IIH) is a rare disorder of PTH-independent hypercalcemia. CYP24A1 and SLC34A1 gene mutations cause two forms of hereditary IIH. In this study, the clinical manifestations and...
7.
Wang L, Su Z, Li Y, Cao B, Su C, Gong C
J Clin Res Pediatr Endocrinol
. 2023 Oct;
16(1):69-75.
PMID: 37847108
Objective: Children born small for gestational age (SGA) are at a greater risk of developing insulin resistance, type 2 diabetes, and cardiovascular disease in adulthood. Gastrointestinal peptides, some secreted by...
8.
Wen X, Fan L, Zhang W, Ni X, Gong C
Asian J Androl
. 2023 Jun;
25(6):731-736.
PMID: 37313883
5α-reductase 2 deficiency prevents testosterone from being converted to dihydrotestosterone, which causes abnormal urogenital sinus development. The aim of this study was to analyze the relationship between genotype-phenotype, surgical selections,...
9.
Ding Y, Wang Q, Gong C
Med Int (Lond)
. 2023 Jan;
2(2):12.
PMID: 36699103
Hyperhomocysteinemia is a common medical condition observed in patients with aminoaciduria. Deficiency in cystathionine beta-synthase, metabolism of cobalamin associated C, peroxiredoxin 1, 5-methyltetrahydrofolate-homocysteine methyltransferase reductase, LMBR1 domain containing 1, 5-methyltetrahydrofolate-homocysteine...
10.
Cheng R, Ying Y, Qiu Z, Fu J, Gong C, Yang Y, et al.
World J Pediatr
. 2022 Dec;
19(5):438-449.
PMID: 36564648
Background: Recombinant human growth hormone (rhGH) therapy has shown to improve height and body composition in children with Prader-Willi syndrome (PWS), the evidence of early rhGH treatment on motor and...