Yang L - Search Results

1

Genotype-Phenotype Correlations in Angelman Syndrome.

Yang L, Shu X, Mao S, Wang Y, Du X, Zou C. Yang L, et al. Genes (Basel). 2021 Jun 28;12(7):987. doi: 10.3390/genes12070987. Genes (Basel). 2021. PMID: 34203304 Free PMC article. Review.

2

Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients.

Yang L, Zhou Q, Ma B, Mao S, Dai Y, Zhu M, Zou C. Yang L, et al. Orphanet J Rare Dis. 2020 Jan 21;15(1):24. doi: 10.1186/s13023-020-1306-z. Orphanet J Rare Dis. 2020. PMID: 31964399 Free PMC article.

3

Ketoacidotic crisis after vaccination in a girl with beta-ketothiolase deficiency: a case report.

Mao S, Yang L, Yin X, Yang J, Huang X. Mao S, et al. Among authors: yang l, yang j. Transl Pediatr. 2021 Feb;10(2):459-463. doi: 10.21037/tp-20-265. Transl Pediatr. 2021. PMID: 33708533 Free PMC article.

4

Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health.

Chao Y, Jiang Y, Zhong M, Wei K, Hu C, Qin Y, Zuo Y, Yang L, Shen Z, Zou C. Chao Y, et al. Among authors: yang l. Cell Biosci. 2021 Apr 1;11(1):66. doi: 10.1186/s13578-021-00581-w. Cell Biosci. 2021. PMID: 33795017 Free PMC article. Review.

5

HbA mutation causing false-normal HbA1c results determined by HPLC in a patient with type 2 diabetes mellitus: A case report.

Wang J, Wang Y, Lv W, Yang L, Huang M, Wang Q. Wang J, et al. Among authors: yang l. Exp Ther Med. 2021 Aug;22(2):845. doi: 10.3892/etm.2021.10277. Epub 2021 Jun 7. Exp Ther Med. 2021. PMID: 34149891 Free PMC article.

6

Do patients with Prader-Willi syndrome have favorable glucose metabolism?

Qian Y, Xia F, Zuo Y, Zhong M, Yang L, Jiang Y, Zou C. Qian Y, et al. Among authors: yang l. Orphanet J Rare Dis. 2022 May 7;17(1):187. doi: 10.1186/s13023-022-02344-3. Orphanet J Rare Dis. 2022. PMID: 35525976 Free PMC article. Review.

7

Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome.

Gao Y, Yang LL, Dai YL, Shen Z, Zhou Q, Zou CC. Gao Y, et al. Orphanet J Rare Dis. 2023 Feb 7;18(1):25. doi: 10.1186/s13023-023-02615-7. Orphanet J Rare Dis. 2023. PMID: 36750945 Free PMC article.

8

Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China.

Mao S, Yang L, Gao Y, Zou C. Mao S, et al. Among authors: yang l. Clin Genet. 2024 Apr;105(4):415-422. doi: 10.1111/cge.14477. Epub 2024 Jan 23. Clin Genet. 2024. PMID: 38258470

9

Publishing trends in World Journal of Pediatric Surgery.

Qi Q, Dorazio R, Yang L, Xie Y, Shu Q. Qi Q, et al. Among authors: yang l. World J Pediatr Surg. 2022 Sep 13;5(4):e000489. doi: 10.1136/wjps-2022-000489. eCollection 2022. World J Pediatr Surg. 2022. PMID: 36474730 Free PMC article. No abstract available.

10

Social responsibilities of a pediatric journal: considerations and future directions.

Yang LL, Wang XJ, Qi Q, Xu SY, Xie YC, Zhao ZY, Shu Q. Yang LL, et al. World J Pediatr. 2021 Feb;17(1):1-2. doi: 10.1007/s12519-021-00416-1. Epub 2021 Feb 4. World J Pediatr. 2021. PMID: 33538946 Free PMC article. No abstract available.

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