Liang H - Search Results

1

Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease.

Liang H, Jiajue R, Qi W, Liu W, Chi Y, Jiang Y, Wang O, Li M, Xing X, Xia W. Liang H, et al. Front Endocrinol (Lausanne). 2022 Oct 20;13:1041061. doi: 10.3389/fendo.2022.1041061. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36339419 Free PMC article.

2

Clinical Characteristics of Short-Stature Patients With an NPR2 Mutation and the Therapeutic Response to rhGH.

Ke X, Liang H, Miao H, Yang H, Wang L, Gong F, Pan H, Zhu H. Ke X, et al. Among authors: liang h. J Clin Endocrinol Metab. 2021 Jan 23;106(2):431-441. doi: 10.1210/clinem/dgaa842. J Clin Endocrinol Metab. 2021. PMID: 33205215

3

Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome.

Li R, Gong F, Pan H, Liang H, Miao H, Zhao Y, Duan L, Yang H, Wang L, Chen S, Zhu H. Li R, et al. Among authors: liang h. Front Endocrinol (Lausanne). 2021 Apr 12;12:605736. doi: 10.3389/fendo.2021.605736. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33912130 Free PMC article.

4

Case Report: A Clinical and Genetic Analysis of Childhood Growth Hormone Deficiency With Familial Hypercholesterolemia.

Yang S, Ke X, Liang H, Li R, Zhu H. Yang S, et al. Among authors: liang h. Front Endocrinol (Lausanne). 2021 Jun 18;12:691490. doi: 10.3389/fendo.2021.691490. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34220717 Free PMC article. Review.

5

A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review.

Li R, Tian B, Liang H, Chen M, Yang H, Wang L, Pan H, Zhu H. Li R, et al. Among authors: liang h. Front Endocrinol (Lausanne). 2021 Sep 30;12:604500. doi: 10.3389/fendo.2021.604500. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34659104 Free PMC article. Review.

6

Clinical, Biochemical, Radiological, Genetic and Therapeutic Analysis of Patients with COMP Gene Variants.

Liang H, Hou Y, Pang Q, Jiang Y, Wang O, Li M, Xing X, Zhu H, Xia W. Liang H, et al. Calcif Tissue Int. 2022 Mar;110(3):313-323. doi: 10.1007/s00223-021-00920-6. Epub 2021 Oct 28. Calcif Tissue Int. 2022. PMID: 34709441

7

Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH.

Chen M, Miao H, Liang H, Ke X, Yang H, Gong F, Wang L, Duan L, Chen S, Pan H, Zhu H. Chen M, et al. Among authors: liang h. Front Endocrinol (Lausanne). 2022 Feb 16;13:820001. doi: 10.3389/fendo.2022.820001. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35250876 Free PMC article.

8

Corrigendum: Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH.

Chen M, Miao H, Liang H, Ke X, Yang H, Gong F, Wang L, Duan L, Chen S, Pan H, Zhu H. Chen M, et al. Among authors: liang h. Front Endocrinol (Lausanne). 2022 Apr 6;13:896742. doi: 10.3389/fendo.2022.896742. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35464067 Free PMC article.

9

Na-Cl Co-transporter (NCC) gene inactivation is associated with improved bone microstructure.

Qi W, Yin Z, Liang H, Chi Y, Liu W, Jiajue R, Jiang Y, Wang O, Li M, Xing X, Tong A, Xia W. Qi W, et al. Among authors: liang h. Osteoporos Int. 2022 Oct;33(10):2193-2204. doi: 10.1007/s00198-022-06471-2. Epub 2022 Jun 29. Osteoporos Int. 2022. PMID: 35767093

10

Jintiange combined with alfacalcidol improves muscle strength and balance in primary osteoporosis: A randomized, double-blind, double-dummy, positive-controlled, multicenter clinical trial.

Liang H, Wang O, Cheng Z, Xia P, Wang L, Shen J, Kong X, Zeng Y, Chao A, Yan L, Lin H, Sun H, Cheng Q, Zhu M, Hu Z, Zhang Z, Tang H, Xia W. Liang H, et al. J Orthop Translat. 2022 Aug 24;35:53-61. doi: 10.1016/j.jot.2022.05.002. eCollection 2022 Jul. J Orthop Translat. 2022. PMID: 36090002 Free PMC article.

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