Wen-bin Zheng
Key Laboratory Of Endocrinology, Chinese Academy Of Medical Sciences And Peking Union Medical College, Shuaifuyuan No. 1, Dongcheng District
Beijing, 100730, China
Beijing, 100730, China
Last Updated: 09/26/2026
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Found 8 publications
The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta.
Journal: Frontiers in endocrinology
Published: March 17, 2022
Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V.
Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V.
Journal: Calcified tissue international
Published: September 22, 2021
A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta.
Journal: Molecular genetics & genomic medicine
Published: July 17, 2020
Effects of Bisphosphonates on Osteoporosis Induced by Duchenne Muscular Dystrophy: A Prospective Study.
Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
Published: February 11, 2020
A novel variant in AIRE causing a rare, non‑classical autoimmune polyendocrine syndrome type 1.
Journal: Molecular medicine reports
Published: November 15, 2019
Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita.
Journal: Molecular genetics & genomic medicine
Published: August 10, 2019
Paralysis Resulting from Calcific Discitis with Acute Herniation.
Journal: Chinese medical journal
Published: October 26, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026