Ren X - Search Results

1

Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families.

Yuan Z, Fan L, Wang Y, Li L, Ren X, Sui S, Song Y, Cheng M, Cao B, Gong C. Yuan Z, et al. Among authors: ren x. Eur J Endocrinol. 2024 Jul 2;191(1):87-96. doi: 10.1093/ejendo/lvae082. Eur J Endocrinol. 2024. PMID: 38938059

2

Increase in Peripheral Blood Intermediate Monocytes is Associated with the Development of Recent-Onset Type 1 Diabetes Mellitus in Children.

Ren X, Mou W, Su C, Chen X, Zhang H, Cao B, Li X, Wu D, Ni X, Gui J, Gong C. Ren X, et al. Int J Biol Sci. 2017 Feb 5;13(2):209-218. doi: 10.7150/ijbs.15659. eCollection 2017. Int J Biol Sci. 2017. PMID: 28255273 Free PMC article.

3

Persistent Müllerian duct syndrome: A case report and review.

Ren X, Wu D, Gong C. Ren X, et al. Exp Ther Med. 2017 Dec;14(6):5779-5784. doi: 10.3892/etm.2017.5281. Epub 2017 Oct 11. Exp Ther Med. 2017. PMID: 29285121 Free PMC article.

4

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. Among authors: ren x. 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.

5

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. Among authors: ren x. 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.

6

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.

7

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients.

Yu C, Xie B, Zhao Z, Zhao S, Liu L, Cheng X, Li X, Cao B, Shao J, Chen J, Zhao H, Yan Z, Su C, Niu Y, Song Y, Wei L, Wang Y, Ren X, Fan L, Zhang B, Li C, Gui B, Zhang Y, Wang L, Chen S, Zhang J, Wu Z, Gong C, Fan X, Wu N. Yu C, et al. Among authors: ren x. Front Endocrinol (Lausanne). 2021 Sep 13;12:711991. doi: 10.3389/fendo.2021.711991. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34589056 Free PMC article.

8

SOX2 heterozygous mutations cause multiple extraocular phenotypes in boys.

Wang Y, Fan L, Ren X, Song Y, Zhang B, Gong C. Wang Y, et al. Among authors: ren x. Chin Med J (Engl). 2021 Nov 10;135(4):477-479. doi: 10.1097/CM9.0000000000001805. Chin Med J (Engl). 2021. PMID: 34759222 Free PMC article. No abstract available.

9

Hormonal changes throughout puberty in boys: an observational study on the treatment outcome of congenital hypogonadotropic hypogonadism.

Ren X, Tian Y, Feng G, Wang Y, Zhang B, Cao B, Chen J, Gong C. Ren X, et al. Chin Med J (Engl). 2021 Oct 21;135(3):362-364. doi: 10.1097/CM9.0000000000001639. Chin Med J (Engl). 2021. PMID: 35108230 Free PMC article. No abstract available.

10

Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study.

Zhao X, Su Z, Chen S, Wang X, Yang Y, Chen L, Liang L, Liu G, Wang Y, Song Y, Fan L, Ren X, Gong C. Zhao X, et al. Among authors: ren x. J Pers Med. 2022 May 10;12(5):771. doi: 10.3390/jpm12050771. J Pers Med. 2022. PMID: 35629193 Free PMC article.

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