Liu L - Search Results

1

[GAA gene variants and genotype-phenotype correlations in patients with glycogen storage disease type Ⅱ].

Huang YL, Sheng HY, Jia XF, Su XY, Zhao XY, Xie T, Tang CF, Liu SC, Li XZ, Zhang W, Mei HF, Zeng CH, Liu L. Huang YL, et al. Among authors: liu sc, liu l. Zhonghua Er Ke Za Zhi. 2021 Mar 2;59(3):189-194. doi: 10.3760/cma.j.cn112140-20200710-00710. Zhonghua Er Ke Za Zhi. 2021. PMID: 33657692 Chinese.

2

[Clinical features and genetics studies of Finnish variant late infantile neuronal ceroid lipofuscinosis in two families].

Zhou ZZ, Li XZ, Cheng J, Zhang W, Zeng CH, Lin YT, Shao YX, Huang YL, Liu L. Zhou ZZ, et al. Among authors: liu l. Zhonghua Er Ke Za Zhi. 2018 Aug 2;56(8):601-604. doi: 10.3760/cma.j.issn.0578-1310.2018.08.009. Zhonghua Er Ke Za Zhi. 2018. PMID: 30078242 Chinese.

3

[Newborn screening program and blood amino acid profiling in early neonates with citrin deficiency].

Tang CF, Liu SC, Feng Y, Mei HF, Liu HP, Feng JW, Ye LX, Wang GQ, Liu L, Huang YL. Tang CF, et al. Among authors: liu sc, liu l, liu hp. Zhonghua Er Ke Za Zhi. 2019 Oct 2;57(10):797-801. doi: 10.3760/cma.j.issn.0578-1310.2019.10.014. Zhonghua Er Ke Za Zhi. 2019. PMID: 31594068 Chinese.

4

[Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou].

Huang YL, Tang CF, Liu SC, Sheng HY, Tang F, Jiang X, Zheng RD, Mei HF, Liu L. Huang YL, et al. Among authors: liu sc, liu l. Zhonghua Er Ke Za Zhi. 2020 Jun 2;58(6):476-481. doi: 10.3760/cma.j.cn112140-20200323-00292. Zhonghua Er Ke Za Zhi. 2020. PMID: 32521959 Chinese.

5

[Phenotypes and ATP7B gene variants in 316 children with Wilson disease].

Lu ZK, Cheng J, Li SM, Lin YT, Zhang W, Li XZ, Sheng HY, Mao XJ, Mei HF, Zheng RD, Liang CL, Jiang MY, Huang YL, Liu L, Zeng CH. Lu ZK, et al. Among authors: liu l. Zhonghua Er Ke Za Zhi. 2022 Apr 2;60(4):317-322. doi: 10.3760/cma.j.cn112140-20210827-00708. Zhonghua Er Ke Za Zhi. 2022. PMID: 35385937 Chinese.

6

[Genetic analysis of TPO, DUOX2 and DUOXA2 genes in children with permanent congenital hypothyroidism suspected dyshormonogenesis].

Huang YL, Tan MY, Jiang X, Li B, Chen QY, Jia XF, Tang CF, Liu JL, Liu L. Huang YL, et al. Among authors: liu jl, liu l. Zhonghua Er Ke Za Zhi. 2017 Mar 2;55(3):210-214. doi: 10.3760/cma.j.issn.0578-1310.2017.03.009. Zhonghua Er Ke Za Zhi. 2017. PMID: 28273705 Chinese.

7

Novel variants and uncommon cases among southern Chinese children with X-linked hypophosphatemia.

Lin Y, Xu J, Li X, Sheng H, Su L, Wu M, Cheng J, Huang Y, Mao X, Zhou Z, Zhang W, Li C, Cai Y, Wu D, Lu Z, Yin X, Zeng C, Liu L. Lin Y, et al. Among authors: liu l. J Endocrinol Invest. 2020 Nov;43(11):1577-1590. doi: 10.1007/s40618-020-01240-6. Epub 2020 Apr 6. J Endocrinol Invest. 2020. PMID: 32253725

8

The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.

Tan M, Huang Y, Jiang X, Li P, Tang C, Jia X, Chen Q, Chen W, Sheng H, Feng Y, Wu D, Liu L. Tan M, et al. Among authors: liu l. Horm Metab Res. 2016 Sep;48(9):581-8. doi: 10.1055/s-0042-112224. Epub 2016 Aug 24. Horm Metab Res. 2016. PMID: 27557340

9

[A case with MPPH3 syndrome caused by a novel variation in CCND2 gene].

Li LF, Zheng X, Liu L, Zhang WC, Xiao MJ, Xie ZH, Li X, Luo SY, Zhang YD, Li DX, Zhang C. Li LF, et al. Among authors: liu l. Zhonghua Er Ke Za Zhi. 2021 Mar 2;59(3):236-237. doi: 10.3760/cma.j.cn112140-20200713-00720. Zhonghua Er Ke Za Zhi. 2021. PMID: 33657702 Chinese.

10

[Effect of treatment with continuous positive airway pressure on nocturnal polyuria in patients with obstructive sleep apnea syndrome].

Liu S, Liu L. Liu S, et al. Among authors: liu l. Zhonghua Jie He He Hu Xi Za Zhi. 2001 Mar;24(3):158-60. Zhonghua Jie He He Hu Xi Za Zhi. 2001. PMID: 11802958 Chinese.

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