Transforming growth factor-β1 gene mutations and phenotypes in pediatric patients with Camurati-Engelmann disease
Author:
Publisher
Spandidos Publications
Subject
Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Camurati–Engelmann Disease: A Case-Based Review About an Ultrarare Bone Dysplasia;European Journal of Rheumatology;2023-03-07
2. Clinical characteristics and identification of a novel TGFB1 variant in three unrelated Chinese families with Camurati‐Engelmann disease;Molecular Genetics & Genomic Medicine;2022-03-21
3. Alendronate disturbs femoral growth due to changes during immunolocalization of transforming growth factor-β1 and bone morphogenetic protein-2 in epiphyseal plate;World Journal of Experimental Medicine;2020-01-08
4. Significant Improvement of Clinical Symptoms, Bone Lesions, and Bone Turnover after Long-Term Zoledronic Acid Treatment in Patients with a Severe Form of Camurati-Engelmann Disease;Molecular Syndromology;2017
5. Clinical diagnosis and mutation analysis of a Chinese family with Camurati-Engelmann disease;Molecular Medicine Reports;2016-12-12
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