Chen L - Search Results

1

Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus.

Jin J, Cao L, Zhao Z, Shen S, Kiess W, Zhi D, Ye R, Cheng R, Chen L, Yang Y, Luo F. Jin J, et al. Among authors: chen l. Eur J Endocrinol. 2007 Dec;157(6):783-7. doi: 10.1530/EJE-07-0393. Eur J Endocrinol. 2007. PMID: 18057387

2

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. Among authors: chen l. Front Genet. 2022 Mar 24;13:833495. doi: 10.3389/fgene.2022.833495. eCollection 2022. Front Genet. 2022. PMID: 35401690 Free PMC article.

3

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report.

Li JQ, Xie XB, Feng JY, Chen L, Abuduxikuer K, Lu Y, Li YC, Wang JS. Li JQ, et al. Among authors: chen l. BMC Gastroenterol. 2018 Jun 25;18(1):96. doi: 10.1186/s12876-018-0827-6. BMC Gastroenterol. 2018. PMID: 29940878 Free PMC article.

4

CXC chemokine receptor 2 is associated with postoperative recurrence and survival of patients with non-metastatic clear-cell renal cell carcinoma.

An H, Xu L, Chang Y, Zhu Y, Yang Y, Chen L, Lin Z, Xu J. An H, et al. Among authors: chen l. Eur J Cancer. 2015 Sep;51(14):1953-61. doi: 10.1016/j.ejca.2015.06.125. Epub 2015 Jul 15. Eur J Cancer. 2015. PMID: 26188847

5

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: chen l. Front Pediatr. 2023 Feb 3;11:1094895. doi: 10.3389/fped.2023.1094895. eCollection 2023. Front Pediatr. 2023. PMID: 36816379 Free PMC article.

6

Clinical features and treatment outcomes of Castleman disease in children: a retrospective cohort in China.

Hu S, Li Z, Wang H, Chen L, Ma Y, Zhu X, Li J, Dong R, Yao W, Dong C, Zhang H, Li K, Dong K, Zhai X. Hu S, et al. Among authors: chen l. Eur J Pediatr. 2023 Dec;182(12):5519-5530. doi: 10.1007/s00431-023-05235-2. Epub 2023 Oct 2. Eur J Pediatr. 2023. PMID: 37782352 Free PMC article. Review.

7

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. Among authors: chen l. Front Genet. 2023 Nov 22;14:1264237. doi: 10.3389/fgene.2023.1264237. eCollection 2023. Front Genet. 2023. PMID: 38075676 Free PMC article.

8

Gastroblastoma in a 12-year-old Chinese boy.

Ma Y, Zheng J, Zhu H, Dong K, Zheng S, Xiao X, Chen L. Ma Y, et al. Among authors: chen l. Int J Clin Exp Pathol. 2014 May 15;7(6):3380-4. eCollection 2014. Int J Clin Exp Pathol. 2014. PMID: 25031764 Free PMC article. Review.

9

[Pentastomiasis of the liver: a case report].

Chen L, Hu XQ. Chen L, et al. Zhonghua Gan Zang Bing Za Zhi. 2007 Jan;15(1):46. Zhonghua Gan Zang Bing Za Zhi. 2007. PMID: 17244459 Chinese. No abstract available.

10

Lateral buttock and postanal congenital dermal sinus tract.

Qi S, Zheng J, Lü Z, Li K, Chen L, Xiao X. Qi S, et al. Among authors: chen l. J Pediatr Surg. 2010 May;45(5):e23-5. doi: 10.1016/j.jpedsurg.2010.02.046. J Pediatr Surg. 2010. PMID: 20438910

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