Fan L - Search Results

1

First Clinical Study on Long-Acting Growth Hormone Therapy in Children with Turner Sydrome.

Gao X, Chen J, Cao B, Dou X, Peng Y, Su C, Qin M, Wei L, Fan L, Zhang B, Gong C. Gao X, et al. Among authors: fan l. Horm Metab Res. 2022 Jun;54(6):389-395. doi: 10.1055/a-1842-0724. Epub 2022 May 3. Horm Metab Res. 2022. PMID: 35504300 Free PMC article.

2

Phenotype and Molecular Characterizations of 30 Children From China With NR5A1 Mutations.

Song Y, Fan L, Gong C. Song Y, et al. Among authors: fan l. Front Pharmacol. 2018 Oct 30;9:1224. doi: 10.3389/fphar.2018.01224. eCollection 2018. Front Pharmacol. 2018. PMID: 30425642 Free PMC article.

3

[Clinical phenotype and gene analysis of 86 cases of 5 alpha reductase deficiency].

Song YN, Fan LJ, Zhao X, Gong CX. Song YN, et al. Among authors: fan lj. Zhonghua Er Ke Za Zhi. 2019 Feb 2;57(2):131-135. doi: 10.3760/cma.j.issn.0578-1310.2019.02.013. Zhonghua Er Ke Za Zhi. 2019. PMID: 30695888 Chinese.

4

New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype-phenotype profiling of SRD5A2 in 190 Chinese patients.

Gui B, Song Y, Su Z, Luo FH, Chen L, Wang X, Chen R, Yang Y, Wang J, Zhao X, Fan L, Liu X, Wang Y, Chen S, Gong C. Gui B, et al. Among authors: fan l. J Med Genet. 2019 Oct;56(10):685-692. doi: 10.1136/jmedgenet-2018-105915. Epub 2019 Jun 11. J Med Genet. 2019. PMID: 31186340

5

Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.

Fan L, Ren X, Song Y, Su C, Fu J, Gong C. Fan L, et al. Orphanet J Rare Dis. 2019 Dec 30;14(1):299. doi: 10.1186/s13023-019-1283-2. Orphanet J Rare Dis. 2019. PMID: 31888681 Free PMC article.

6

Aromatase deficiency: A case series of 46, XX Chinese children and a systematic review of the literature.

Fan L, Zhang B, Li L, Gong C. Fan L, et al. Clin Endocrinol (Oxf). 2020 Dec;93(6):687-695. doi: 10.1111/cen.14277. Epub 2020 Jul 27. Clin Endocrinol (Oxf). 2020. PMID: 32623730

7

Clinical and molecular spectrum of 46,XY disorders of sex development that harbour MAMLD1 variations: case series and review of literature.

Li L, Su C, Fan L, Gao F, Liang X, Gong C. Li L, et al. Among authors: fan l. Orphanet J Rare Dis. 2020 Jul 20;15(1):188. doi: 10.1186/s13023-020-01459-9. Orphanet J Rare Dis. 2020. PMID: 32690052 Free PMC article. Review.

8

Clinical characteristics and genotype-phenotype correlations of 130 Chinese children in a high-homogeneity single-center cohort with 5α-reductase 2 deficiency.

Fan L, Song Y, Polak M, Li L, Ren X, Zhang B, Wu D, Gong C. Fan L, et al. Mol Genet Genomic Med. 2020 Oct;8(10):e1431. doi: 10.1002/mgg3.1431. Epub 2020 Jul 26. Mol Genet Genomic Med. 2020. PMID: 32713132 Free PMC article.

9

Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance.

Li L, Gao F, Fan L, Su C, Liang X, Gong C. Li L, et al. Among authors: fan l. Front Endocrinol (Lausanne). 2020 Dec 23;11:582516. doi: 10.3389/fendo.2020.582516. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 33424767 Free PMC article.

10

Efficacy and safety of human chorionic gonadotropin combined with human menopausal gonadotropin and a gonadotropin-releasing hormone pump for male adolescents with congenital hypogonadotropic hypogonadism.

Liu Y, Ren XY, Peng YG, Chen SK, Cheng XR, Qin M, Wang XL, Song YN, Fan LJ, Gong CX. Liu Y, et al. Chin Med J (Engl). 2021 Mar 31;134(10):1152-1159. doi: 10.1097/CM9.0000000000001419. Chin Med J (Engl). 2021. PMID: 33813517 Free PMC article.

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