Wei H - Search Results

1

A High Proportion of Novel ACAN Mutations and Their Prevalence in a Large Cohort of Chinese Short Stature Children.

Lin L, Li M, Luo J, Li P, Zhou S, Yang Y, Chen K, Weng Y, Ge X, Mireguli M, Wei H, Yang H, Li G, Sun Y, Cui L, Zhang S, Chen J, Zeng G, Xu L, Luo X, Shen Y. Lin L, et al. Among authors: wei h. J Clin Endocrinol Metab. 2021 Jun 16;106(7):e2711-e2719. doi: 10.1210/clinem/dgab088. J Clin Endocrinol Metab. 2021. PMID: 33606014 Free PMC article.

2

[Association between single nucleotide polymorphism of insulin-like growth factor receptor gene and idiopathic short stature].

Huang H, Yang Y, Wang W, Yang L, Xie LL, Wang Y, Wei HY. Huang H, et al. Among authors: wei hy. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Dec;13(12):955-8. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 22172258 Free article. Chinese.

3

Status and trends of diabetes in Chinese children: analysis of data from 14 medical centers.

Fu JF, Liang L, Gong CX, Xiong F, Luo FH, Liu GL, Li P, Liu L, Xin Y, Yao H, Cui LW, Shi X, Yang Y, Chen LQ, Wei HY. Fu JF, et al. Among authors: wei hy. World J Pediatr. 2013 May;9(2):127-34. doi: 10.1007/s12519-013-0414-4. Epub 2013 May 16. World J Pediatr. 2013. PMID: 23677831

4

[Clinical characteristics and therapy of idiopathic hypoparathyroidism in 30 infants].

Yang HH, Chen YX, Wei HY. Yang HH, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Oct;17(10):1137-9. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 26483239 Free article. Chinese. No abstract available.

5

IGF1R Variants in Patients With Growth Impairment: Four Novel Variants and Genotype-Phenotype Correlations.

Yang L, Xu DD, Sun CJ, Wu J, Wei HY, Liu Y, Zhang MY, Luo FH. Yang L, et al. J Clin Endocrinol Metab. 2018 Nov 1;103(11):3939-3944. doi: 10.1210/jc.2017-02782. J Clin Endocrinol Metab. 2018. PMID: 30053089

6

[Protective effect of vitamin A on residual pancreatic β cell function in children with type 1 diabetes mellitus].

Chen YX, Chen Q, Zhang YX, Liu F, Yang HH, Wu SN, Wei HY. Chen YX, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Dec;20(12):1020-1023. doi: 10.7499/j.issn.1008-8830.2018.12.008. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30572991 Free PMC article. Chinese.

7

Sirolimus Therapy and Follow-up in a Patient with Severe Congenital Hyperinsulinism Following Subtotal Pancreatectomy.

Chen Q, Chen Y, Wang X, Yang H, Zhang Y, Liu X, Yan Y, Wei H. Chen Q, et al. Among authors: wei h. J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):119-123. doi: 10.4274/jcrpe.galenos.2020.2020.0033. Epub 2020 Jun 2. J Clin Res Pediatr Endocrinol. 2021. PMID: 32482020 Free PMC article.

8

A novel stop-loss DAX1 variant affecting its protein-interaction with SF1 precedes the adrenal hypoplasia congenital with rare spontaneous precocious puberty and elevated hypothalamic-pituitary-gonadal/adrenal axis responses.

Yang H, Wei H, Shen L, Kumar C S, Chen Q, Chen Y, Kumar SA. Yang H, et al. Among authors: wei h. Eur J Med Genet. 2021 May;64(5):104192. doi: 10.1016/j.ejmg.2021.104192. Epub 2021 Mar 23. Eur J Med Genet. 2021. PMID: 33766795

9

HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration.

Sun Y, Wei X, Fang F, Shen Y, Wei H, Li J, Ye X, Zhan Y, Ye X, Liu X, Yang W, Li Y, Geng X, Huang X, Ruan Y, Qin Z, Yi S, Lyu J, Fang H, Yu Y. Sun Y, et al. Among authors: wei x, wei h. J Genet Genomics. 2021 Aug 20;48(8):727-736. doi: 10.1016/j.jgg.2021.01.009. Epub 2021 Jun 17. J Genet Genomics. 2021. PMID: 34334354

10

[Clinical and genetic analysis of an infant with aldosterone synthase deficiency].

Yang H, Chen Q, Zhang L, Cui Y, Wei H. Yang H, et al. Among authors: wei h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Sep 10;38(9):865-868. doi: 10.3760/cma.j.cn511374-20200302-00121. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34487532 Chinese.

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