Wang XM - Search Results

1

What can we do for the adolescents with polycystic ovary syndrome?

Chen Y, Tang YJ, Li X, Wang XM. Chen Y, et al. Among authors: wang xm. World J Pediatr. 2024 Nov 30. doi: 10.1007/s12519-024-00857-4. Online ahead of print. World J Pediatr. 2024. PMID: 39614993 No abstract available.

2

Genotypic and phenotypic features of dyslipidemia in a sample of pediatric patients in China.

Zhang Q, Chang G, Tang Y, Gu S, Ding Y, Chen Y, Wang Y, Liu S, Wang J, Wang X. Zhang Q, et al. BMC Pediatr. 2023 Mar 29;23(1):138. doi: 10.1186/s12887-023-03952-z. BMC Pediatr. 2023. PMID: 36991406 Free PMC article.

3

Sex-specific difference in phenotype of Kabuki syndrome type 2 patients: a matched case-control study.

Wang Y, Xu Y, Chen Y, Hu Y, Li Q, Liu S, Wang J, Wang X. Wang Y, et al. BMC Pediatr. 2024 Feb 19;24(1):133. doi: 10.1186/s12887-024-04562-z. BMC Pediatr. 2024. PMID: 38373926 Free PMC article.

4

Screening/diagnosis of pediatric endocrine disorders through the artificial intelligence model in different language settings.

Ying L, Li S, Chen C, Yang F, Li X, Chen Y, Ding Y, Chang G, Li J, Wang X. Ying L, et al. Eur J Pediatr. 2024 Jun;183(6):2655-2661. doi: 10.1007/s00431-024-05527-1. Epub 2024 Mar 19. Eur J Pediatr. 2024. PMID: 38502320 Free PMC article.

5

Clinical characteristics and genetic expansion of 46,XY disorders of sex development children in a Chinese prospective study.

Tang Y, Chen Y, Wang J, Zhang Q, Wang Y, Xu Y, Li X, Wang J, Wang X. Tang Y, et al. Endocr Connect. 2023 Sep 4;12(10):e230029. doi: 10.1530/EC-23-0029. Print 2023 Oct 1. Endocr Connect. 2023. PMID: 37493574 Free PMC article.

6

[Clinical characteristics and genetic analysis of a patient with STISS syndrome due to variant of PSMD12 gene].

Xu L, Wang Y, Zhang Q, Chen Y, Chang G, Wang X, Wang J, Ding Y. Xu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Mar 10;40(3):349-353. doi: 10.3760/cma.j.cn511374-20220207-00097. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36854413 Review. Chinese.

7

[Identification of a child with Teebi hypertelorism syndrome 1 due to variant of SPECC1L gene].

Li Z, Wang Y, Li X, Feng B, Gu S, Yang F, Chang G, Wang J, Wang X. Li Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Aug 10;40(8):998-1003. doi: 10.3760/cma.j.cn511374-20220823-00574. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37532501 Chinese.

8

Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients.

Feng B, Li X, Zhang Q, Wang Y, Gu S, Yao RE, Li Z, Gao S, Chang G, Li Q, Li N, Fu L, Wang J, Wang X. Feng B, et al. Orphanet J Rare Dis. 2023 Sep 11;18(1):284. doi: 10.1186/s13023-023-02878-0. Orphanet J Rare Dis. 2023. PMID: 37697378 Free PMC article.

9

[Treatment of ornithine transcarbamylase deficiency in a child with glyceryl phenylbutyrate].

Yang F, Wang LR, Li X, Hu JY, Ying LW, Feng BY, Li YY, Lin KN, She JX, Li H, Chang GY, Wang XM. Yang F, et al. Among authors: wang lr, wang xm. Zhongguo Dang Dai Er Ke Za Zhi. 2024 May 15;26(5):512-517. doi: 10.7499/j.issn.1008-8830.2310050. Zhongguo Dang Dai Er Ke Za Zhi. 2024. PMID: 38802913 Free PMC article. Chinese.

10

Complex clinical manifestations and new insights in RNA sequencing of children with diabetes and WFS1 variants.

Ding Y, Li Z, Zhang Q, Li N, Chang G, Wang Y, Li X, Li J, Li Q, Yao RE, Li X, Wang X. Ding Y, et al. Front Endocrinol (Lausanne). 2023 Mar 7;14:1066320. doi: 10.3389/fendo.2023.1066320. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36967753 Free PMC article.

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