Liu L - Search Results

1

Effect of Hormone Replacement Therapy on Bone Mineral Density and Body Composition in Chinese Adolescent and Young Adult Turner Syndrome Patients.

Li L, Qiu X, Lash GE, Yuan L, Liang Z, Liu L. Li L, et al. Among authors: liu l. Front Endocrinol (Lausanne). 2019 Jun 12;10:377. doi: 10.3389/fendo.2019.00377. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31244781 Free PMC article.

2

Body composition and bone mineral status in patients with Turner syndrome.

Shi K, Liu L, He YJ, Li D, Yuan LX, Lash GE, Li L. Shi K, et al. Among authors: liu l. Sci Rep. 2016 Nov 30;6:38026. doi: 10.1038/srep38026. Sci Rep. 2016. PMID: 27901060 Free PMC article. Clinical Trial.

3

Epidermal growth factor and tumor necrosis factor α cooperatively promote the motility of hepatocellular carcinoma cell lines via synergistic induction of fibronectin by NF-κB/p65.

Liu ZC, Ning F, Wang HF, Chen DY, Cai YN, Sheng HY, Lash GE, Liu L, Du J. Liu ZC, et al. Among authors: liu l. Biochim Biophys Acta Gen Subj. 2017 Nov;1861(11 Pt A):2568-2582. doi: 10.1016/j.bbagen.2017.08.010. Epub 2017 Aug 24. Biochim Biophys Acta Gen Subj. 2017. PMID: 28844984

4

Rare copy number variants in the genome of Chinese female children and adolescents with Turner syndrome.

Li L, Li Q, Wang Q, Liu L, Li R, Liu H, He Y, Lash GE. Li L, et al. Among authors: liu h, liu l. Biosci Rep. 2019 Jan 11;39(1):BSR20181305. doi: 10.1042/BSR20181305. Print 2019 Jan 31. Biosci Rep. 2019. PMID: 30530863 Free PMC article.

5

Phenotype and molecular characteristics in 45 Chinese children with 5α-reductase type 2 deficiency from South China.

Cheng J, Lin R, Zhang W, Liu G, Sheng H, Li X, Zhou Z, Mao X, Liu L. Cheng J, et al. Among authors: liu l, liu g. Clin Endocrinol (Oxf). 2015 Oct;83(4):518-26. doi: 10.1111/cen.12799. Epub 2015 May 7. Clin Endocrinol (Oxf). 2015. PMID: 25899528

6

Novel mutations in a Chinese family with two patients with succinic semialdehyde dehydrogenase deficiency.

Chen XD, Lin YT, Jiang MY, Li XZ, Li D, Hu H, Liu L. Chen XD, et al. Among authors: liu l. Gynecol Endocrinol. 2020 Oct;36(10):929-933. doi: 10.1080/09513590.2020.1744555. Epub 2020 Mar 30. Gynecol Endocrinol. 2020. PMID: 32223457 Free article.

7

[Clinical and molecular analysis of two Chinese siblings with Cockayne syndrome].

Zhou Z, Liu L, Wu M, Liu H, Cai Y, Sheng H, Li X, Cheng J, Li D, Huang Y. Zhou Z, et al. Among authors: liu h, liu l. Zhonghua Er Ke Za Zhi. 2016 Jan;54(1):56-60. doi: 10.3760/cma.j.issn.0578-1310.2016.01.013. Zhonghua Er Ke Za Zhi. 2016. PMID: 26791926 Chinese.

8

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy.

Su X, Lin R, Huang Y, Sheng H, Li X, Ting TH, Liu L, Li X. Su X, et al. Among authors: liu l. J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):52-57. doi: 10.4274/jcrpe.3556. Epub 2016 Sep 9. J Clin Res Pediatr Endocrinol. 2017. PMID: 27612026 Free PMC article.

9

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China.

Xu A, Cheng J, Sheng H, Wen Z, Lin Y, Zhou Z, Zeng C, Shao Y, Li C, Liu L, Li X. Xu A, et al. Among authors: liu l. J Clin Res Pediatr Endocrinol. 2019 Nov 22;11(4):400-409. doi: 10.4274/jcrpe.galenos.2019.2019.0046. Epub 2019 Jun 18. J Clin Res Pediatr Endocrinol. 2019. PMID: 31208162 Free PMC article.

10

'Isolated' germline mosaicism in the phenotypically normal father of a girl with X-linked hypophosphatemic rickets.

Lin Y, Cai Y, Xu J, Zeng C, Sheng H, Yu Y, Li X, Liu L. Lin Y, et al. Among authors: liu l. Eur J Endocrinol. 2020 Jan;182(1):K1-K6. doi: 10.1530/EJE-19-0472. Eur J Endocrinol. 2020. PMID: 31658436

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