Bei F - Search Results

1

Application of Next-Generation Sequencing for Genetic Diagnosis in Neonatal Intensive Care Units: Results of a Multicenter Study in China.

Zhu T, Gong X, Bei F, Ma L, Chen Y, Zhang Y, Wang X, Sun J, Wang J, Qiu G, Sun J, Sun Y, Zhang Y. Zhu T, et al. Among authors: bei f. Front Genet. 2020 Nov 6;11:565078. doi: 10.3389/fgene.2020.565078. eCollection 2020. Front Genet. 2020. PMID: 33240318 Free PMC article.

2

Two novel isovaleryl-CoA dehydrogenase gene mutations in a Chinese infant.

Bei F, Sun JH, Yu YG, Jia J, Zheng ZJ, Fu QH, Cai W. Bei F, et al. Gene. 2013 Jul 25;524(2):396-400. doi: 10.1016/j.gene.2013.03.139. Epub 2013 Apr 12. Gene. 2013. PMID: 23587913

3

Long-term effect of early postnatal overnutrition on insulin resistance and serum fatty acid profiles in male rats.

Bei F, Jia J, Jia YQ, Sun JH, Liang F, Yu ZY, Cai W. Bei F, et al. Lipids Health Dis. 2015 Aug 26;14:96. doi: 10.1186/s12944-015-0094-2. Lipids Health Dis. 2015. PMID: 26302954 Free PMC article.

4

Carbamoyl phosphate synthetase 1 deficiency diagnosed by whole exome sequencing.

Zhang G, Chen Y, Ju H, Bei F, Li J, Wang J, Sun J, Bu J. Zhang G, et al. Among authors: bei f. J Clin Lab Anal. 2018 Feb;32(2):e22241. doi: 10.1002/jcla.22241. Epub 2017 Apr 26. J Clin Lab Anal. 2018. PMID: 28444906 Free PMC article.

5

Variations in melatonin levels in preterm and term human breast milk during the first month after delivery.

Qin Y, Shi W, Zhuang J, Liu Y, Tang L, Bu J, Sun J, Bei F. Qin Y, et al. Among authors: bei f. Sci Rep. 2019 Nov 29;9(1):17984. doi: 10.1038/s41598-019-54530-2. Sci Rep. 2019. PMID: 31784629 Free PMC article.

6

[Neonatal capillary malformation-arteriovenous malformation complicated with acute heart failure: a case report and literature review].

Wang LJ, Sun JH, Bei F. Wang LJ, et al. Among authors: bei f. Zhonghua Er Ke Za Zhi. 2020 Jul 2;58(7):591-595. doi: 10.3760/cma.j.cn112140-20200312-00221. Zhonghua Er Ke Za Zhi. 2020. PMID: 32605345 Review. Chinese.

7

Primary immunodeficiency-related genes in neonatal intensive care unit patients with various genetic immune abnormalities: a multicentre study in China.

Zhu T, Gong X, Bei F, Ma L, Sun J, Wang J, Qiu G, Sun J, Sun Y, Zhang Y. Zhu T, et al. Among authors: bei f. Clin Transl Immunology. 2021 Mar 22;10(3):e1266. doi: 10.1002/cti2.1266. eCollection 2021. Clin Transl Immunology. 2021. PMID: 33777394 Free PMC article.

8

Exposure to air pollutants during pregnancy and after birth increases the risk of neonatal hyperbilirubinemia.

Zhuang J, Hu J, Bei F, Huang J, Wang L, Zhao J, Qian R, Sun J. Zhuang J, et al. Among authors: bei f. Environ Res. 2022 Apr 15;206:112523. doi: 10.1016/j.envres.2021.112523. Epub 2021 Dec 18. Environ Res. 2022. PMID: 34929187

9

A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis.

Dong S, Bei F, Yu T, Sun L, Chen X, Yan H. Dong S, et al. Among authors: bei f. Front Genet. 2022 Feb 28;13:814511. doi: 10.3389/fgene.2022.814511. eCollection 2022. Front Genet. 2022. PMID: 35295944 Free PMC article.

10

Association of preterm outcome with maternal systemic lupus erythematosus: a retrospective cohort study.

Chen X, Di W, Ye L, Hu Y, Jiang M, Wu J, Bu J, Sun J, Bei F. Chen X, et al. Among authors: bei f. Ital J Pediatr. 2023 Apr 1;49(1):43. doi: 10.1186/s13052-023-01436-5. Ital J Pediatr. 2023. PMID: 37005645 Free PMC article.

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