Chen D - Search Results

1

[SLC22A5 gene mutation analysis and prenatal diagnosis for a family with primary carnitine deficiency].

Tan J, Chen D, Li Z, Yuan D, Liu B, Yan T, Huang J, Cai R. Tan J, et al. Among authors: chen d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):690-693. doi: 10.3760/cma.j.issn.1003-9406.2019.07.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302912 Chinese.

2

[An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency].

Tan JQ, Chen DY, Li ZT, Huang JW, Yan TZ, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Oct;18(10):1019-1025. doi: 10.7499/j.issn.1008-8830.2016.10.021. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27751224 Free PMC article. Chinese.

3

[Pancytopenia and metabolic decompensation in a neonate].

Tan JQ, Chen DY, Mo ZQ, Li ZT, Huang JW, Cai R, Yan TZ. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Nov;18(11):1150-1153. doi: 10.7499/j.issn.1008-8830.2016.11.019. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27817783 Free PMC article. Chinese.

4

[CPT2 gene mutation analysis and prenatal diagnosis in a family with carnitine palmitoyltransferase II deficiency].

Tan JQ, Chen DY, Li WG, Li ZT, Huang JW, Yan TZ, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2016 Dec;18(12):1282-1285. doi: 10.7499/j.issn.1008-8830.2016.12.017. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27974123 Free PMC article. Chinese.

5

[Genetic diagnosis of 10 neonates with primary carnitine deficiency].

Tan JQ, Chen DY, Li ZT, Yan TZ, Huang JW, Cai R. Tan JQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Nov;19(11):1150-1154. doi: 10.7499/j.issn.1008-8830.2017.11.005. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 29132460 Free PMC article. Chinese.

6

[Screening indices and their cut-off values for full-term neonates carrying β-thalassemia gene].

Yang JL, Cai R, Chen DY, Tan JQ, Huang LH. Yang JL, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Dec;20(12):990-993. doi: 10.7499/j.issn.1008-8830.2018.12.003. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30572986 Free PMC article. Chinese.

7

[Analysis of CGDH gene variants and clinical features in three patients with glutaric aciduria type Ⅰ].

Tan J, Chen D, Yan T, Huang J, Cai R. Tan J, et al. Among authors: chen d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):882-885. doi: 10.3760/cma.j.issn.1003-9406.2019.09.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515781 Chinese.

8

[Tandem mass spectrometry analysis and genetic diagnosis of neonates with fatty acid oxidation disorders in central and northern regions of Guangxi].

Tan J, Chen D, Huang J, Chang R, Yan T, Cai R. Tan J, et al. Among authors: chen d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1067-1072. doi: 10.3760/cma.j.issn.1003-9406.2019.11.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31703127 Chinese.

9

Tandem Mass Spectrometry Screening for Inborn Errors of Metabolism in Newborns and High-Risk Infants in Southern China: Disease Spectrum and Genetic Characteristics in a Chinese Population.

Tan J, Chen D, Chang R, Pan L, Yang J, Yuan D, Huang L, Yan T, Ning H, Wei J, Cai R. Tan J, et al. Among authors: chen d. Front Genet. 2021 Jul 28;12:631688. doi: 10.3389/fgene.2021.631688. eCollection 2021. Front Genet. 2021. PMID: 34394177 Free PMC article.

10

Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations.

Yang J, Yuan D, Tan X, Zeng Y, Tang N, Chen D, Tan J, Cai R, Huang J, Yan T. Yang J, et al. Among authors: chen d. Mol Med Rep. 2022 Feb;25(2):47. doi: 10.3892/mmr.2021.12563. Epub 2021 Dec 8. Mol Med Rep. 2022. PMID: 34878152 Free PMC article.

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