Tang F - Search Results

1

[Screening Abnormal Hemoglobin Diseases for Couples of Childbearing Age in Guangzhou City by HPLC].

Chen GL, Qu YX, Jiang F, Tang Y, Tang F, Zuo LD. Chen GL, et al. Among authors: tang f, tang y. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Dec;25(6):1768-1771. doi: 10.7534/j.issn.1009-2137.2017.06.034. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017. PMID: 29262913 Chinese.

2

Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report.

Jiang H, Jiang F, Li J, Tang F, Li DZ. Jiang H, et al. Among authors: tang f. Hemoglobin. 2019 Jul-Sep;43(4-5):292-295. doi: 10.1080/03630269.2019.1680384. Epub 2019 Oct 23. Hemoglobin. 2019. PMID: 31645145

3

[Evaluations of newborn screening program performance and enzymatic diagnosis of glucose-6-phosphate dehydrogenase deficiency in Guangzhou].

Tang F, Huang YL, Jiang X, Jia XF, Li B, Feng Y, Chen QY, Tang CF. Tang F, et al. Among authors: tang cf. Zhonghua Er Ke Za Zhi. 2018 May 2;56(5):359-363. doi: 10.3760/cma.j.issn.0578-1310.2018.05.010. Zhonghua Er Ke Za Zhi. 2018. PMID: 29783822 Chinese.

4

[Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou].

Huang YL, Tang CF, Liu SC, Sheng HY, Tang F, Jiang X, Zheng RD, Mei HF, Liu L. Huang YL, et al. Among authors: tang f, tang cf. Zhonghua Er Ke Za Zhi. 2020 Jun 2;58(6):476-481. doi: 10.3760/cma.j.cn112140-20200323-00292. Zhonghua Er Ke Za Zhi. 2020. PMID: 32521959 Chinese.

5

[Correlation analysis of genotypes and the enzymatic activities of glucose-6-phosphate dehydrogenase in neonates in Guangzhou].

Tang F, Tang CF, Jiang X, Jia XF, Liu SC, Chen QY, Huang YL. Tang F, et al. Among authors: tang cf. Zhonghua Yu Fang Yi Xue Za Zhi. 2020 Nov 6;54(11):1275-1282. doi: 10.3760/cma.j.cn112150-20200611-00864. Zhonghua Yu Fang Yi Xue Za Zhi. 2020. PMID: 33147929 Chinese.

6

Screening for neonatal inherited metabolic disorders by tandem mass spectrometry in Guangzhou.

Tang C, Tan M, Xie T, Tang F, Liu S, Wei Q, Liu J, Huang Y. Tang C, et al. Among authors: tang f. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2021 Aug 25;50(4):463-471. doi: 10.3724/zdxbyxb-2021-0260. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2021. PMID: 34704419 Free PMC article. English.

7

The adjustment of 17-hydroxyprogesterone cut-off values for congenital adrenal hyperplasia neonatal screening by GSP according to gestational age and age at sampling.

Jiang X, Tang F, Feng Y, Li B, Jia X, Tang C, Liu S, Huang Y. Jiang X, et al. Among authors: tang f, tang c. J Pediatr Endocrinol Metab. 2019 Nov 26;32(11):1253-1258. doi: 10.1515/jpem-2019-0140. J Pediatr Endocrinol Metab. 2019. PMID: 31603856

8

A pilot study of newborn screening for X-linked adrenoleukodystrophy based on liquid chromatography-tandem mass spectrometry method for detection of C26:0-lysophosphatidylcholine in dried blood spots: Results from 43,653 newborns in a southern Chinese population.

Tang C, Tang F, Cai Y, Tan M, Liu S, Xie T, Jiang X, Huang Y. Tang C, et al. Among authors: tang f. Clin Chim Acta. 2024 Jan 1;552:117653. doi: 10.1016/j.cca.2023.117653. Epub 2023 Nov 15. Clin Chim Acta. 2024. PMID: 37977233

9

Detection of glucosylsphingosine in dried blood spots for diagnosis of Gaucher disease by LC-MS/MS.

Tang C, Jia X, Tang F, Liu S, Jiang X, Zhao X, Sheng H, Peng M, Liu L, Huang Y. Tang C, et al. Among authors: tang f. Clin Biochem. 2021 Jan;87:79-84. doi: 10.1016/j.clinbiochem.2020.10.011. Epub 2020 Nov 11. Clin Biochem. 2021. PMID: 33188770

10

Identification of an inherited pathogenic DNAJC12 variant in a patient with hyperphenylalalinemia.

Feng Y, Liu S, Tang C, Jiang X, Tang F, Li B, Jia X, Chen Q, Liu J, Huang Y. Feng Y, et al. Among authors: tang f, tang c. Clin Chim Acta. 2019 Mar;490:172-175. doi: 10.1016/j.cca.2018.09.002. Epub 2018 Sep 1. Clin Chim Acta. 2019. PMID: 30179615

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