Zhang B - Search Results

1

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. Among authors: zhang b. Clin Endocrinol (Oxf). 2020 Dec;93(6):687-695. doi: 10.1111/cen.14277. Epub 2020 Jul 27. Clin Endocrinol (Oxf). 2020. PMID: 32623730

2

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: zhang b. 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.

3

Variant analysis of the chromodomain helicase DNA-binding protein 7 in pediatric disorders of sex development.

Zhang B, Song Y, Li W, Gong C. Zhang B, et al. Pediatr Investig. 2019 Mar 22;3(1):31-38. doi: 10.1002/ped4.12111. eCollection 2019 Mar. Pediatr Investig. 2019. PMID: 32851286 Free PMC article.

4

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: zhang b, zhang j, zhang y. 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.

5

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: zhang b. 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.

6

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. Among authors: zhang b. 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.

7

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: zhang b. 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.

8

DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing.

Fan X, Zhang B, Fan L, Chen J, Su C, Cao B, Wei L, Qin M, Gong C. Fan X, et al. Among authors: zhang b. J Pers Med. 2022 May 26;12(6):872. doi: 10.3390/jpm12060872. J Pers Med. 2022. PMID: 35743657 Free PMC article.

9

Correction: 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: zhang b. Horm Metab Res. 2022 Jun;54(6):e5. doi: 10.1055/a-2008-2304. Epub 2023 Jan 13. Horm Metab Res. 2022. PMID: 36638815 Free PMC article. No abstract available.

10

Sifrim-Hitz-Weiss/CHD4-related syndrome: A new case report.

Zhang B, Cheng M, Fan L, Gong C. Zhang B, et al. Pediatr Investig. 2023 Jan 4;7(2):137-139. doi: 10.1002/ped4.12357. eCollection 2023 Jun. Pediatr Investig. 2023. PMID: 37324594 Free PMC article. No abstract available.

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