Li JY - Search Results

1

Children with infectious pneumonia caused by Ralstonia insidiosa: A case report.

Lin SZ, Qian MJ, Wang YW, Chen QD, Wang WQ, Li JY, Yang RT, Wang XY, Mu CY, Jiang K. Lin SZ, et al. Among authors: li jy. World J Clin Cases. 2023 Mar 26;11(9):2002-2008. doi: 10.12998/wjcc.v11.i9.2002. World J Clin Cases. 2023. PMID: 36998962 Free PMC article.

2

Novel compound heterozygous variants in the TAF6 gene in a patient with Alazami-Yuan syndrome: A case report.

Lin SZ, Feng JH, Sun LP, Ma HW, Wang WQ, Li JY. Lin SZ, et al. Among authors: li jy. World J Clin Cases. 2022 Feb 26;10(6):1889-1895. doi: 10.12998/wjcc.v10.i6.1889. World J Clin Cases. 2022. PMID: 35317131 Free PMC article.

3

Clinical manifestations and gene analysis of Hutchinson-Gilford progeria syndrome: A case report.

Zhang SL, Lin SZ, Zhou YQ, Wang WQ, Li JY, Wang C, Pang QM. Zhang SL, et al. Among authors: li jy. World J Clin Cases. 2022 May 26;10(15):5018-5024. doi: 10.12998/wjcc.v10.i15.5018. World J Clin Cases. 2022. PMID: 35801028 Free PMC article.

4

Case report: Heterogeneous mutations of SOX10 gene in a Chinese infant with Waardenburg syndrome type 4C.

Zhang S, Lin S, Liu Z, Wang W, Li J, Chen Q, Yang L, Wang C, Pang Q. Zhang S, et al. Front Pediatr. 2022 Aug 22;10:898693. doi: 10.3389/fped.2022.898693. eCollection 2022. Front Pediatr. 2022. PMID: 36071884 Free PMC article.

5

VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report.

Wu XH, Lin SZ, Zhou YQ, Wang WQ, Li JY, Chen QD. Wu XH, et al. Among authors: li jy. World J Clin Cases. 2022 Aug 26;10(24):8749-8754. doi: 10.12998/wjcc.v10.i24.8749. World J Clin Cases. 2022. PMID: 36157797 Free PMC article.

6

Novel frameshift mutation in the AHDC1 gene in a Chinese global developmental delay patient: A case report.

Lin SZ, Xie HY, Qu YL, Gao W, Wang WQ, Li JY, Feng XC, Jin CQ. Lin SZ, et al. Among authors: li jy. World J Clin Cases. 2022 Jul 26;10(21):7517-7522. doi: 10.12998/wjcc.v10.i21.7517. World J Clin Cases. 2022. PMID: 36157999 Free PMC article.

7

Two novel mutations in the VPS33B gene in a Chinese patient with arthrogryposis, renal dysfunction and cholestasis syndrome 1: A case report.

Yang H, Lin SZ, Guan SH, Wang WQ, Li JY, Yang GD, Zhang SL. Yang H, et al. Among authors: li jy. World J Clin Cases. 2022 Oct 26;10(30):11016-11022. doi: 10.12998/wjcc.v10.i30.11016. World J Clin Cases. 2022. PMID: 36338198 Free PMC article.

8

Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report.

Lin SZ, Ma QJ, Pang QM, Chen QD, Wang WQ, Li JY, Zhang SL. Lin SZ, et al. Among authors: li jy. World J Clin Cases. 2022 Nov 6;10(31):11486-11492. doi: 10.12998/wjcc.v10.i31.11486. World J Clin Cases. 2022. PMID: 36387827 Free PMC article.

9

Retroperitoneal leiomyoma located in the broad ligament: A case report.

Zhang XS, Lin SZ, Liu YJ, Zhou L, Chen QD, Wang WQ, Li JY. Zhang XS, et al. Among authors: li jy. World J Clin Cases. 2022 Nov 16;10(32):12022-12027. doi: 10.12998/wjcc.v10.i32.12022. World J Clin Cases. 2022. PMID: 36405292 Free PMC article.

10

A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report.

Qian M, Lin S, Tan Y, Chen Q, Wang W, Li J, Mu C. Qian M, et al. Medicine (Baltimore). 2023 Apr 7;102(14):e33457. doi: 10.1097/MD.0000000000033457. Medicine (Baltimore). 2023. PMID: 37026922 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,306 results

Search Page

Filters