Treatment of Osteogenesis Imperfecta: Who, Why, What?
Author:
Publisher
S. Karger AG
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Reference28 articles.
1. Osteogenesis imperfecta
2. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta
3. Genetic heterogeneity in osteogenesis imperfecta.
4. Osteogenesis imperfecta in childhood: Treatment strategies
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1. Application of Orthopantomography in the Analysis of Bone Mineral Density in Patients with Osteogenesis Imperfecta;Applied Sciences;2024-02-27
2. Temporal analysis of therapeutic approaches to osteogenesis imperfecta in the context of pediatric orthopedics - an update;International Journal of Pregnancy & Child Birth;2023-12-20
3. Treatment with neridronate in children and adolescents with osteogenesis imperfecta: Data from open-label, not controlled, three-year Italian study;Bone;2017-10
4. Osteogenesis imperfecta in children and adolescents—new developments in diagnosis and treatment;Osteoporosis International;2016-08-05
5. Decreased fracture rate, pharmacogenetics and BMD response in 79 Swedish children with osteogenesis imperfecta types I, III and IV treated with Pamidronate;Bone;2016-06
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