Zeng C - Search Results

1

Natural history and outcome of nonketotic hyperglycinemia in China.

Zhou Z, Cai Y, Li X, Liu Z, Peng M, Lin Y, Mao X, Zeng C, Liu L, Zhang W. Zhou Z, et al. Among authors: zeng c. Front Neurol. 2024 Aug 14;15:1440883. doi: 10.3389/fneur.2024.1440883. eCollection 2024. Front Neurol. 2024. PMID: 39206282 Free PMC article.

2

Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China.

Liu Z, Zhao X, Sheng H, Cai Y, Yin X, Chen X, Su L, Lu Z, Zeng C, Li X, Liu L. Liu Z, et al. Among authors: zeng c. Am J Med Genet A. 2018 Mar;176(3):589-596. doi: 10.1002/ajmg.a.38601. Epub 2018 Jan 23. Am J Med Genet A. 2018. PMID: 29359854

3

Clinical features and mutational analysis in 114 young children with Wilson disease from South China.

Li X, Lu Z, Lin Y, Lu X, Xu Y, Cheng J, Shao Y, Su X, Liu Z, Sheng H, Cai Y, Li T, Zhou Z, Tan J, Liu H, Huang Y, Liu L, Zeng C. Li X, et al. Among authors: zeng c. Am J Med Genet A. 2019 Aug;179(8):1451-1458. doi: 10.1002/ajmg.a.61254. Epub 2019 Jun 6. Am J Med Genet A. 2019. PMID: 31172689

4

Features of chinese patients with sitosterolemia.

Zhou Z, Su X, Cai Y, Ting TH, Zhang W, Lin Y, Xu A, Mao X, Zeng C, Liu L, Li X. Zhou Z, et al. Among authors: zeng c. Lipids Health Dis. 2022 Jan 18;21(1):11. doi: 10.1186/s12944-021-01619-1. Lipids Health Dis. 2022. PMID: 35042526 Free PMC article. Review.

5

[Phenotypes and ATP7B gene variants in 316 children with Wilson disease].

Lu ZK, Cheng J, Li SM, Lin YT, Zhang W, Li XZ, Sheng HY, Mao XJ, Mei HF, Zheng RD, Liang CL, Jiang MY, Huang YL, Liu L, Zeng CH. Lu ZK, et al. Among authors: zeng ch. Zhonghua Er Ke Za Zhi. 2022 Apr 2;60(4):317-322. doi: 10.3760/cma.j.cn112140-20210827-00708. Zhonghua Er Ke Za Zhi. 2022. PMID: 35385937 Chinese.

6

Thyroid function in children with Prader-Willi syndrome in Southern China: a single-center retrospective case series.

Huang X, Yin X, Wu D, Cai Y, Li X, Zhang W, Zeng C, Mao X, Liu L. Huang X, et al. Among authors: zeng c. BMC Pediatr. 2022 Apr 29;22(1):234. doi: 10.1186/s12887-022-03275-5. BMC Pediatr. 2022. PMID: 35488223 Free PMC article.

7

Clinical characteristics and long-term outcomes of 12 children with vitamin D-dependent rickets type 1A: A retrospective study.

Lin Y, Guan Z, Mei H, Zhang W, Zhou Z, Su L, Cheng J, Zheng R, Liang C, Cai Y, Yin X, Wu D, Liu L, Zeng C. Lin Y, et al. Among authors: zeng c. Front Pediatr. 2022 Nov 4;10:1007219. doi: 10.3389/fped.2022.1007219. eCollection 2022. Front Pediatr. 2022. PMID: 36405822 Free PMC article.

8

Features of BSCL2 related congenital generalized lipodystrophy in China: long-term follow-up of three patients and literature review.

Su X, Lin Y, Liu L, Mei H, Xu A, Zeng C, Sheng H, Cheng J, Shao Y, Zheng R, Ting TH, Zhang W, Li X. Su X, et al. Among authors: zeng c. J Pediatr Endocrinol Metab. 2022 Nov 28;36(1):74-80. doi: 10.1515/jpem-2022-0372. Print 2023 Jan 27. J Pediatr Endocrinol Metab. 2022. PMID: 36433712 Review.

9

Diagnosis of an intermediate case of maple syrup urine disease: A case report.

Lin YT, Cai YN, Ting TH, Liu L, Zeng CH, Su L, Peng MZ, Li XZ. Lin YT, et al. World J Clin Cases. 2023 Feb 16;11(5):1077-1085. doi: 10.12998/wjcc.v11.i5.1077. World J Clin Cases. 2023. PMID: 36874425 Free PMC article.

10

Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome.

Lin Y, Chen X, Xie B, Guan Z, Chen X, Li X, Yi P, Du R, Mei H, Liu L, Zhang W, Zeng C. Lin Y, et al. Among authors: zeng c. Front Genet. 2023 Mar 21;14:1085210. doi: 10.3389/fgene.2023.1085210. eCollection 2023. Front Genet. 2023. PMID: 37025457 Free PMC article.

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