Ruoqian Cheng
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Explore the profile of Ruoqian Cheng including associated specialties, affiliations and a list of published articles.
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24
Citations
133
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Recent Articles
11.
Sun C, Lu B, Liu Y, Zhang Y, Wei H, Hu X, et al.
Front Endocrinol (Lausanne)
. 2021 Dec;
12:779365.
PMID: 34899612
Context: Long-acting recombinant human growth hormone (rhGH) has transformed growth hormone deficiency (GHD) treatment. However, the possibility and rationality for flexible time regimen are pending. Objective: We studied the efficacy...
12.
Chang Z, Lu W, Zhao Z, Xi L, Li X, Ye R, et al.
BMC Med Genomics
. 2021 Jul;
14(1):172.
PMID: 34193132
Background: Primary adrenal insufficiency (PAI) is life-threatening, and a definitive aetiological diagnosis is essential for management and prognostication. We conducted this study to investigate the genetic aetiologies of PAI in...
13.
You J, Cheng X, Li X, Li M, Yao L, Luo F, et al.
BMC Endocr Disord
. 2021 Apr;
21(1):75.
PMID: 33879124
Background: The gold standard for the diagnosis of central precocious puberty (CPP) is gonadotropin-releasing hormone (GnRH) or GnRH analogs (GnRHa) stimulation test. But the stimulation test is time-consuming and costly....
14.
Zhang M, Sun C, Liu R, Dong C, Cheng R, Zheng Z, et al.
Transl Pediatr
. 2020 Nov;
9(5):653-661.
PMID: 33209728
Background: Beckwith-Wiedemann syndrome (BWS) is primarily caused by epigenetic errors. This study aimed to analyze the relationship between the epigenetic errors and phenotypes of BWS and to evaluate the efficacy...
15.
Ni J, Ge J, Zhang M, Hussain K, Guan Y, Cheng R, et al.
Eur J Pediatr
. 2019 Jun;
178(8):1161-1169.
PMID: 31218401
Congenital hyperinsulinism (CHI) is a clinically, genetically, and morphologically heterogeneous disorder. F DOPA-PET CT scanning greatly improves its clinical outcome. Here, we presented the first Chinese F DOPA-PET CT scanning-based...
16.
Xu D, Sun C, Zhou Z, Wu B, Yang L, Chang Z, et al.
BMC Med Genet
. 2018 May;
19(1):79.
PMID: 29769040
Background: Mutations in the aggrecan (ACAN) gene can cause short stature (with heterogeneous clinical phenotypes), impaired bone maturation, and large variations in response to growth hormone (GH) treatment. For such...
17.
Xu D, Lu L, Xi L, Cheng R, Pei Z, Bi Y, et al.
J Pediatr Endocrinol Metab
. 2017 Nov;
30(12):1285-1291.
PMID: 29176021
Background: Exogenous androgen supplement is an optional treatment for micropenis; however, its use in childhood is controversial due to potential side effects. Methods: Twenty-three children (mean age: 4.07±3.4 years) with...
18.
Sun C, Pei Z, Zhang M, Sun B, Yang L, Zhao Z, et al.
J Diabetes
. 2017 Apr;
10(1):50-58.
PMID: 28371426
Background: Solute carrier family 19 member 2 (SLC19A2) gene deficiency is one of the causes of permanent neonatal diabetes mellitus (PNDM) and can be effectively managed by thiamine supplementation. Herein...
19.
Sun C, Wei H, Chen X, Zhao Z, Du H, Song W, et al.
Meta Gene
. 2016 Jun;
9:120-3.
PMID: 27331016
Type 1 diabetes (T1D) is an autoimmune disease that has strong contribution of genetic factors to its etiology. We aimed to assess the genetic association between non-HLA genes and T1D...
20.
Zheng Z, Cao L, Pei Z, Zhi D, Zhao Z, Xi L, et al.
Int J Clin Exp Med
. 2015 Jul;
8(5):7965-70.
PMID: 26221355
The aim of this study is to investigate the frequency distribution of exon 3 deleted (d3-GHR) genetic polymorphism of growth hormone receptor (GHR) in growth hormone deficient (GHD) Chinese children...