Liu L - Search Results

1

Dynamics alteration of the gut microbiota and faecal metabolomes in very low or extremely low birth weight infants: a Chinese single-center, prospective cohort study.

Liu L, Chen C, Li Y, Ao D, Wu J, Cai N, Li W, Xiang M. Liu L, et al. Front Microbiol. 2024 Aug 23;15:1438213. doi: 10.3389/fmicb.2024.1438213. eCollection 2024. Front Microbiol. 2024. PMID: 39247697 Free PMC article.

2

RNA-binding proteins in degenerative joint diseases: A systematic review.

Xiang M, Liu L, Wu T, Wei B, Liu H. Xiang M, et al. Among authors: liu h, liu l. Ageing Res Rev. 2023 Apr;86:101870. doi: 10.1016/j.arr.2023.101870. Epub 2023 Feb 4. Ageing Res Rev. 2023. PMID: 36746279 Review.

3

Antenatal steroid as an independent risk factor for vitamin K2 deficiency in newborns: A Chinese single-center, retrospective study.

Liu L, Chen CH, Rong SW, Lin SZ, Cai NL, Ao D. Liu L, et al. Saudi Med J. 2023 Aug;44(8):788-794. doi: 10.15537/smj.2023.44.8.20230084. Saudi Med J. 2023. PMID: 37582573 Free PMC article.

4

Multi-omics analyses of gut microbiota via 16S rRNA gene sequencing, LC-MS/MS and diffusion tension imaging reveal aberrant microbiota-gut-brain axis in very low or extremely low birth weight infants with white matter injury.

Liu L, Xiang M, Cai X, Wu B, Chen C, Cai N, Ao D. Liu L, et al. BMC Microbiol. 2023 Dec 6;23(1):387. doi: 10.1186/s12866-023-03103-5. BMC Microbiol. 2023. PMID: 38057706 Free PMC article.

5

[Clinical phenotype and genetic analysis of a child with Intellectual developmental disorder and epilepsy due to variant of CLTC gene].

Xie Z, Li C, Chen C, Huang B, Liu L, Ao D. Xie Z, et al. Among authors: liu l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Jul 10;41(7):817-820. doi: 10.3760/cma.j.cn511374-20230515-00288. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38946364 Chinese.

6

Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay.

Li C, Wang Y, Zeng C, Huang B, Chen Y, Xue C, Liu L, Rong S, Lin Y. Li C, et al. Among authors: liu l. Sci Rep. 2024 Nov 11;14(1):27590. doi: 10.1038/s41598-024-79431-x. Sci Rep. 2024. PMID: 39528574 Free PMC article.

7

[Clinical and genetic characteristics of a child with Developmental and epileptic encephalopathy 104 due to variant of ATP6V0A1 gene].

Li C, Wang Y, Chen S, Rong S, Huang B, Liu L, Lou H. Li C, et al. Among authors: liu l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Mar 10;41(3):345-350. doi: 10.3760/cma.j.cn511374-20221221-00881. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38448027 Review. Chinese.

8

Infantile Rosai-Dorfman disease: an unusual case of neck swelling and a literature review.

Liu L, Huang Y, Zeng C. Liu L, et al. Int J Clin Exp Pathol. 2020 Dec 1;13(12):3187-3191. eCollection 2020. Int J Clin Exp Pathol. 2020. PMID: 33425120 Free PMC article.

9

Serum 25-hydroxyvitamin D status of a large Chinese population from 30 provinces by LC-MS/MS measurement for consecutive 3 years: differences by age, sex, season and province.

Bai K, Dong H, Liu L, She X, Liu C, Yu M, Liang Z, Lin H, Ke P, Huang X, Wu X, Zhang Q, Zhao B. Bai K, et al. Among authors: liu l, liu c. Eur J Nutr. 2023 Apr;62(3):1503-1516. doi: 10.1007/s00394-023-03094-z. Epub 2023 Jan 24. Eur J Nutr. 2023. PMID: 36692589

10

[Clinical and genetic analysis of three children with Menkes disease due to variants of ATP7A gene].

Wang Z, Chen Q, Wang Y, Liu L, Li C. Wang Z, et al. Among authors: liu l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Jun 10;40(6):668-673. doi: 10.3760/cma.j.cn511374-20220816-00550. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37212000 Chinese.

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