Fang Y - Search Results

1

Neonatal sclerosing cholangitis with novel mutations in DCDC2 (doublecortin domain-containing protein 2) in Chinese children.

Wei X, Fang Y, Wang JS, Wang YZ, Zhang Y, Abuduxikuer K, Chen L. Wei X, et al. Among authors: fang y. Front Pediatr. 2023 Feb 3;11:1094895. doi: 10.3389/fped.2023.1094895. eCollection 2023. Front Pediatr. 2023. PMID: 36816379 Free PMC article.

2

Functional Polymorphisms in hOGG1 Gene and Neuroblastoma Risk in Chinese Children.

Wang YZ, Zhuo ZJ, Fang Y, Li L, Zhang J, He J, Wu XM. Wang YZ, et al. Among authors: fang y. J Cancer. 2018 Oct 31;9(23):4521-4526. doi: 10.7150/jca.27983. eCollection 2018. J Cancer. 2018. PMID: 30519358 Free PMC article.

3

TP53 Arg72Pro polymorphism and neuroblastoma susceptibility in eastern Chinese children: a three-center case-control study.

Fang Y, Wu X, Li L, Zhu J, Wu H, Zhou H, He J, Wang Y. Fang Y, et al. Biosci Rep. 2020 May 29;40(5):BSR20200854. doi: 10.1042/BSR20200854. Biosci Rep. 2020. PMID: 32406493 Free PMC article.

4

Correlation between the genetic variants of base excision repair (BER) pathway genes and neuroblastoma susceptibility in eastern Chinese children.

Zhuo Z, Zhou C, Fang Y, Zhu J, Lu H, Zhou H, Wu H, Wang Y, He J. Zhuo Z, et al. Among authors: fang y. Cancer Commun (Lond). 2020 Nov;40(11):641-646. doi: 10.1002/cac2.12088. Epub 2020 Aug 11. Cancer Commun (Lond). 2020. PMID: 32780923 Free PMC article. No abstract available.

5

TMEM199-Congenital Disorder of Glycosylation With Novel Phenotype and Genotype in a Chinese Boy.

Fang Y, Abuduxikuer K, Wang YZ, Li SM, Chen L, Wang JS. Fang Y, et al. Front Genet. 2022 Mar 24;13:833495. doi: 10.3389/fgene.2022.833495. eCollection 2022. Front Genet. 2022. PMID: 35401690 Free PMC article.

6

Infant-Type Hemispheric Glioma in a Chinese Girl: A Newly Defined Entity.

Fang Y, Wang YZ, Wei X, Li SM, Chen L. Fang Y, et al. Fetal Pediatr Pathol. 2023 Feb;42(1):114-122. doi: 10.1080/15513815.2022.2061659. Epub 2022 Apr 11. Fetal Pediatr Pathol. 2023. PMID: 35404193

7

A Case Series of Pediatric Intestinal Ganglioneuromatosis With Novel Phenotypic and Genotypic Profile.

Fang Y, Zhang Y, Dong R, Wang YZ, Chen L, Chen G. Fang Y, et al. Front Med (Lausanne). 2022 Jun 16;9:883958. doi: 10.3389/fmed.2022.883958. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35783634 Free PMC article.

8

Synchronous Hepatoblastoma and Neuroblastoma in Two Chinese Infants.

Shao B, Wang YZ, Fang Y, Chu J, Chen L, He LJ. Shao B, et al. Among authors: fang y. Fetal Pediatr Pathol. 2023 Aug;42(4):690-698. doi: 10.1080/15513815.2023.2186696. Epub 2023 Mar 17. Fetal Pediatr Pathol. 2023. PMID: 36930961

9

Expanding the phenotype and metabolic basis of ATP6AP2-congenital disorder of glycosylation in a Chinese patient with a novel variant c.185G>A (p.Gly62Glu).

Fang Y, Wang YZ, Chen L, Xie XB. Fang Y, et al. Front Genet. 2023 Nov 22;14:1264237. doi: 10.3389/fgene.2023.1264237. eCollection 2023. Front Genet. 2023. PMID: 38075676 Free PMC article.

10

Two case reports of mixed epithelial and stromal renal tumor of kidney in children and literature review analysis.

Wei X, Wang Y, Fang Y, Chen L. Wei X, et al. Among authors: fang y. Indian J Pathol Microbiol. 2023 Oct-Dec;66(4):845-847. doi: 10.4103/ijpm.ijpm_148_22. Indian J Pathol Microbiol. 2023. PMID: 38084545 Free article. Review.

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