Li M - Search Results

1

The roles of sclerostin and irisin on bone and muscle of orchiectomized rats.

Zhou BN, Zhang Q, Lin XY, Hu J, Zhao DC, Jiang Y, Xing XP, Li M. Zhou BN, et al. Among authors: li m. BMC Musculoskelet Disord. 2022 Dec 2;23(1):1049. doi: 10.1186/s12891-022-05982-7. BMC Musculoskelet Disord. 2022. PMID: 36456918 Free PMC article.

2

Primary hyperparathyroidism in Chinese children and adolescents: A single-centre experience at Peking Union Medical College Hospital.

Wang W, Kong J, Nie M, Jiang Y, Li M, Xia W, Meng X, Xing X, Wang O. Wang W, et al. Among authors: li m. Clin Endocrinol (Oxf). 2017 Dec;87(6):865-873. doi: 10.1111/cen.13453. Epub 2017 Sep 13. Clin Endocrinol (Oxf). 2017. PMID: 28833384

3

Clinical and genetic characteristics of Pseudohypoparathyroidism in the Chinese population.

Chu X, Zhu Y, Wang O, Nie M, Quan T, Xue Y, Wang W, Jiang Y, Li M, Xia W, Xing X. Chu X, et al. Among authors: li m. Clin Endocrinol (Oxf). 2018 Feb;88(2):285-294. doi: 10.1111/cen.13516. Epub 2017 Dec 14. Clin Endocrinol (Oxf). 2018. PMID: 29136292

4

Effects of alendronate and alfacalcidol on bone in patients with myasthenia gravis initiating glucocorticoids treatment.

Lv F, Guan Y, Ma D, Xu X, Song Y, Li L, Jiang Y, Wang O, Xia W, Xing X, Li M. Lv F, et al. Among authors: li m, li l. Clin Endocrinol (Oxf). 2018 Mar;88(3):380-387. doi: 10.1111/cen.13537. Epub 2018 Jan 12. Clin Endocrinol (Oxf). 2018. PMID: 29266368

5

A novel missense mutation in P4HB causes mild osteogenesis imperfecta.

Li L, Zhao D, Zheng W, Wang O, Jiang Y, Xia W, Xing X, Li M. Li L, et al. Among authors: li m. Biosci Rep. 2019 Apr 30;39(4):BSR20182118. doi: 10.1042/BSR20182118. Print 2019 May 31. Biosci Rep. 2019. PMID: 30948499 Free PMC article.

6

Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA.

Wang Y, Nie M, Wang O, Li Y, Jiang Y, Li M, Xia W, Xing X. Wang Y, et al. Among authors: li y, li m. J Bone Miner Res. 2019 Dec;34(12):2254-2263. doi: 10.1002/jbmr.3854. Epub 2019 Nov 13. J Bone Miner Res. 2019. PMID: 31433868 Free article.

7

Nonremission and Recurrent Tumor-Induced Osteomalacia: A Retrospective Study.

Li X, Jiang Y, Huo L, Wu H, Liu Y, Jin J, Yu W, Lv W, Zhou L, Xia Y, Wang O, Li M, Xing X, Chi Y, Jiajue R, Cui L, Meng X, Xia W. Li X, et al. Among authors: li m. J Bone Miner Res. 2020 Mar;35(3):469-477. doi: 10.1002/jbmr.3903. Epub 2019 Nov 15. J Bone Miner Res. 2020. PMID: 31643101 Free PMC article.

8

Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita.

Zheng WB, Li LJ, Zhao DC, Wang O, Jiang Y, Xia WB, Xing XP, Li M. Zheng WB, et al. Among authors: li lj, li m. Mol Genet Genomic Med. 2020 Mar;8(3):e1139. doi: 10.1002/mgg3.1139. Epub 2020 Jan 23. Mol Genet Genomic Med. 2020. PMID: 31972903 Free PMC article.

9

Age-, Site-, and Sex-Specific Normative Centile Curves for HR-pQCT-Derived Microarchitectural and Bone Strength Parameters in a Chinese Mainland Population.

Yu F, Xu Y, Hou Y, Lin Y, Jiajue R, Jiang Y, Wang O, Li M, Xing X, Zhang L, Qin L, Hsieh E, Xia W. Yu F, et al. Among authors: li m. J Bone Miner Res. 2020 Nov;35(11):2159-2170. doi: 10.1002/jbmr.4116. Epub 2020 Jul 21. J Bone Miner Res. 2020. PMID: 32564403 Free PMC article.

10

A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta.

Hu J, Li LJ, Zheng WB, Zhao DC, Wang O, Jiang Y, Xing XP, Li M, Xia W. Hu J, et al. Among authors: li lj, li m. Mol Genet Genomic Med. 2020 Dec;8(12):e1525. doi: 10.1002/mgg3.1525. Epub 2020 Nov 9. Mol Genet Genomic Med. 2020. PMID: 33166085 Free PMC article.

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