Zhu WB - Search Results

1

Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis.

Zhou JF, Luo JY, Zhu WB, Yang CY, Zeng YL, Qiu XL. Zhou JF, et al. Among authors: zhu wb. J Matern Fetal Neonatal Med. 2021 Jan;34(1):12-23. doi: 10.1080/14767058.2019.1570115. Epub 2019 Jan 30. J Matern Fetal Neonatal Med. 2021. PMID: 30700176

2

Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.

Zhou J, Yang C, Zhu W, Chen S, Zeng Y, Wang J, Zhao H, Chen Y, Lin F. Zhou J, et al. Biomed Res Int. 2018 Sep 12;2018:7803175. doi: 10.1155/2018/7803175. eCollection 2018. Biomed Res Int. 2018. PMID: 30298137 Free PMC article.

3

[Risk factors of 125 cases of neonatal congenital hypothyroidism during perinatal period].

Zhou J, Luo J, Zhao H, Wang J, Lin F, Zhang H, Su Y, Chen Y, Zeng Y, Lin Q, Zhu W. Zhou J, et al. Zhonghua Liu Xing Bing Xue Za Zhi. 2015 Jul;36(7):747-51. Zhonghua Liu Xing Bing Xue Za Zhi. 2015. PMID: 26564707 Chinese.

4

[Association of thyroperoxidase gene polymorphisms with dyshormonogenesis in congenital hypothyroidism].

Su Y, Wang J, Zhou J, Chen Y, Zhao H, Zeng Y, Lin F, Zhang H, Zhu W, Chen H. Su Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):861-5. doi: 10.3760/cma.j.issn.1003-9406.2015.06.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663066 Chinese.

5

Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian.

Chen Y, Xiu W, Dong Y, Wang J, Zhao H, Su Y, Zhou J, Zeng Y, Li H, Wo J, Lin F, Zhang H, Chen H, Yang C, Zhu W. Chen Y, et al. Medicine (Baltimore). 2018 Jul;97(30):e11553. doi: 10.1097/MD.0000000000011553. Medicine (Baltimore). 2018. PMID: 30045279 Free PMC article.

6

A verification of the application of the non-derivatized mass spectrometry method in newborns screening of metabolic disorders.

Zheng Y, Chen Y, Qiu X, Chen W, Lin Q, Zeng Y, Zhao H, Zhu W. Zheng Y, et al. Medicine (Baltimore). 2019 May;98(19):e15500. doi: 10.1097/MD.0000000000015500. Medicine (Baltimore). 2019. PMID: 31083189 Free PMC article.

7

Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China.

Zhou J, Luo J, Lin J, Zeng Y, Qiu X, Zhu W, Liu G. Zhou J, et al. Medicine (Baltimore). 2020 Jun 26;99(26):e20838. doi: 10.1097/MD.0000000000020838. Medicine (Baltimore). 2020. PMID: 32590776 Free PMC article.

8

Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency.

Chen Y, Lin Q, Zeng Y, Qiu X, Liu G, Zhu W. Chen Y, et al. Mol Genet Genomic Med. 2021 Feb;9(2):e1583. doi: 10.1002/mgg3.1583. Epub 2021 Feb 9. Mol Genet Genomic Med. 2021. PMID: 33560599 Free PMC article.

9

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian.

Chen Y, Lin X, Lin Q, Zeng Y, Qiu X, Liu G, Zhu W. Chen Y, et al. Medicine (Baltimore). 2021 Mar 12;100(10):e24161. doi: 10.1097/MD.0000000000024161. Medicine (Baltimore). 2021. PMID: 33725819 Free PMC article.

10

[Analysis of GCDH gene mutations in 3 patients from Fujian area with glutaric academia type I].

Chen Y, Lin Q, Zeng Y, Zhao H, Chen W, Zhou J, Su Y, Lin F, Zhang H, Zhu W. Chen Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):657-660. doi: 10.3760/cma.j.issn.1003-9406.2018.05.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30298489 Chinese.

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