Chen C - Search Results

1

Comprehensive newborn screening for severe combined immunodeficiency, X-linked agammaglobulinemia, and spinal muscular atrophy: the Chinese experience.

Chen C, Zhang C, Wu DW, Wang BY, Xiao R, Huang XL, Yang X, Gao ZG, Yang RL. Chen C, et al. World J Pediatr. 2024 Dec;20(12):1270-1282. doi: 10.1007/s12519-024-00846-7. Epub 2024 Nov 5. World J Pediatr. 2024. PMID: 39500858 Free PMC article.

2

Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China.

Zhang T, Shen Y, Xu Y, Wu D, Chen C, Yang R. Zhang T, et al. Among authors: chen c. Clin Chim Acta. 2023 Jul 1;547:117459. doi: 10.1016/j.cca.2023.117459. Epub 2023 Jun 28. Clin Chim Acta. 2023. PMID: 37390946

3

Long-term follow-up of children with carbamoyl phosphate synthase 1 deficiency detected in newborn screening.

Zhang Z, Tong F, Chen C, Zhang T, Qian G, Yang X, Huang X, Yang R, Zhao Z. Zhang Z, et al. Among authors: chen c. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Nov 14;52(6):721-726. doi: 10.3724/zdxbyxb-2023-0359. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 37986659 Free PMC article. Chinese, English.

4

Genotypic and phenotypic spectrum of maple syrup urine disease in Zhejiang of China.

Yang X, Yang R, Zhang T, Tan DJ, Pan R, Chen Z, Wu D, Chen C, Xu Y, Zhang L, Li X, Shu Q, Hu L. Yang X, et al. Among authors: chen z, chen c. QJM. 2024 Oct 1;117(10):717-727. doi: 10.1093/qjmed/hcae104. QJM. 2024. PMID: 38837343 Free PMC article.

5

Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China.

Tong F, Zhang Y, Chen C, Zhu L, Lu Y, Zhang Z, Chen T, Yan J, Zheng J, Zhao X, Zhou D, Yang X, Yang R, Cang X, Jiang P, Shu Q. Tong F, et al. Among authors: chen c, chen t. Front Cell Dev Biol. 2023 Jan 10;10:1059680. doi: 10.3389/fcell.2022.1059680. eCollection 2022. Front Cell Dev Biol. 2023. PMID: 36704196 Free PMC article.

6

[Analysis of clinical features, biochemical indices and genetic variants among children with Short/branched-chain acyl-CoA dehydrogenase deficiency detected by neonatal screening].

Zhao H, Zhou D, Miao H, Chen C, Yang J, Yang R, Huang X. Zhao H, et al. Among authors: chen c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Feb 10;40(2):155-160. doi: 10.3760/cma.j.cn511376-20220318-00179. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36709932 Chinese.

7

Newborn screening for inherited metabolic diseases using tandem mass spectrometry in China: Outcome and cost-utility analysis.

Zhao Z, Chen C, Sun X, Zhou D, Huang X, Dong H. Zhao Z, et al. Among authors: chen c. J Med Screen. 2022 Mar;29(1):12-20. doi: 10.1177/09691413211021621. Epub 2021 Jun 9. J Med Screen. 2022. PMID: 34102920

8

Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Feng J, Yang C, Zhu L, Zhang Y, Zhao X, Chen C, Chen QX, Shu Q, Jiang P, Tong F. Feng J, et al. Among authors: chen c, chen qx. Orphanet J Rare Dis. 2021 Sep 20;16(1):392. doi: 10.1186/s13023-021-02018-6. Orphanet J Rare Dis. 2021. PMID: 34544473 Free PMC article. Review.

9

Correction to: Phenotype, genotype and long-term prognosis of 40 Chinese patients with isobutyryl-CoA dehydrogenase deficiency and a review of variant spectra in ACAD8.

Feng J, Yang C, Zhu L, Zhang Y, Zhao X, Chen C, Chen QX, Shu Q, Jiang P, Tong F. Feng J, et al. Among authors: chen c, chen qx. Orphanet J Rare Dis. 2021 Dec 7;16(1):505. doi: 10.1186/s13023-021-02132-5. Orphanet J Rare Dis. 2021. PMID: 34876202 Free PMC article. No abstract available.

10

TRIM22-Mediated Apoptosis is Associated with Bak Oligomerization in Monocytes.

Chen C, Zhao D, Fang S, Chen Q, Cheng B, Fang X, Shu Q. Chen C, et al. Among authors: chen q. Sci Rep. 2017 Jan 12;7:39961. doi: 10.1038/srep39961. Sci Rep. 2017. PMID: 28079123 Free PMC article.

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