Zhi-Ya Dong
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Explore the profile of Zhi-Ya Dong including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
8
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0
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Recent Articles
1.
Zhao X, Lu W, Li W, Wang J, Dong Z, Xiao Y, et al.
Zhongguo Dang Dai Er Ke Za Zhi
. 2025 Feb;
27(2):199-204.
PMID: 39962783
Objectives: To explore the application of the colloidal gold method and chemiluminescence method in detecting gonadotropin (Gn) in morning urine for assessing pubertal development status in children. Methods: A total...
2.
Lu W, Ma X, Zhang J, Wang J, Zhang T, Ye L, et al.
World J Pediatr
. 2024 Jan;
PMID: 38240902
No abstract available.
3.
Lu W, Ma X, Zhang J, Wang J, Zhang T, Ye L, et al.
World J Pediatr
. 2023 Jul;
20(4):422-433.
PMID: 37486441
Background: The clinical manifestations of nonclassical 11beta-hydroxylase deficiency are very similar to those of non-classical 21-hydroxylase deficiency. For this study, we investigated the relationship between the clinical and molecular features...
4.
Zhang J, Wang J, Xu X, Zhang L, Zhang C, Lu W, et al.
Front Pediatr
. 2022 Oct;
10:960825.
PMID: 36210930
Introduction: The frequency of celiac disease autoantibody (CDAb) positivity in type 1 diabetes (T1D) has increased due to unclear mechanisms, including autoimmune injury. Circular ribonucleic acids (circRNAs) participate in autoimmune...
5.
Zhang J, Wang J, Sun M, Xu D, Xiao Y, Lu W, et al.
World J Clin Cases
. 2021 May;
9(13):3200-3211.
PMID: 33969109
Background: Alström syndrome (AS, OMIM ID 203800) is a rare disease involving multiple organs in children and is mostly reported in non-Chinese patients. In the Chinese population, there are few...
6.
Chang G, Dong Z, Wang W, Xiao Y, Chen F, Ni J, et al.
Zhonghua Er Ke Za Zhi
. 2011 Sep;
49(6):451-4.
PMID: 21924060
Objective: To analyze clinical characteristics of children with 45, X/46, XY mosaicism and explore effective managements for them. Method: Five children with 45, X/46, XY mosaicism were all in puberty...
7.
Chang G, Dong Z, Wang W, Wang D
Zhonghua Er Ke Za Zhi
. 2011 Jan;
48(12):944-6.
PMID: 21215191
Objective: To elucidate the curative and adverse effect of recombinant human growth hormone (rhGH) in 2 patients with isolated-growth hormone deficiency type IA (IGHDIA), to track sexual development and pregnancy,...
8.
Chen Y, Wang W, Wang X, Dong Z, Xiao Y, Ni J, et al.
Zhonghua Er Ke Za Zhi
. 2009 Dec;
47(10):789-91.
PMID: 20021817
Objective: To detect CYP17A1 gene mutation in a patient with 17 alpha-hydroxylase/17, 20-lyase deficiency and her family members. Method: Genomic DNA was extracted from the blood of the patient, her...
9.
Xiao Y, Yang J, Zhang H, Wang W, Li X, Wang D, et al.
Zhonghua Er Ke Za Zhi
. 2008 Mar;
45(12):937-41.
PMID: 18339285
Objective: Inactivating mutations of DAX-1 give rise to the X-linked form of adrenal hypoplasia congenita (AHC). Affected individuals are at risk of early postnatal Addisonian crisis, but the variable phenotypic...
10.
Wang W, Wang D, Cui Y, Ni J, Dong Z, Fu M, et al.
Zhonghua Er Ke Za Zhi
. 2004 Jan;
41(6):453-6.
PMID: 14749005
Objective: Prader-Willi syndrome (PWS) is an example of a human genetic disorder that involves imprinting genes on the proximal long arm of chromosome 15 and SNRPN gene as a candidate...