Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations — genotype–phenotype correlations and effect of bisphosphonate treatment-Reference-Cited by-同舟云学术

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Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations — genotype–phenotype correlations and effect of bisphosphonate treatment

Published:2016-05 Issue: Volume:86 Page:53-57
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Sato Atsuko,Ouellet Jean,Muneta Takeshi,Glorieux Francis H.,Rauch Frank

Funder

Fonds de Recherche du Québec – Santé

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference31 articles.

1. New genes in bone development: what's new in osteogenesis imperfecta;Marini;J. Clin. Endocrinol. Metab.,2013

2. Vertebral morphometry in children and adolescents with osteogenesis imperfecta: effect of intravenous pamidronate treatment;Land;Bone,2006

3. Reshaping of vertebrae during treatment with neridronate or pamidronate in children with osteogenesis imperfecta;Semler;Horm. Res. Paediatr.,2011

4. Intravenous bisphosphonate therapy of young children with osteogenesis imperfecta: skeletal findings during follow up throughout the growing years;Palomo;J. Bone Miner. Res.,2015

5. Scoliosis in osteogenesis imperfecta;Renshaw;Clin. Orthop. Relat. Res.,1979

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4. The Role of Denosumab and Bisphosphonate in Osteogenesis Imperfecta: A Literature Review;Salud, Ciencia y Tecnología;2024-04-04

5. Medical Management for Fracture Prevention in Children with Osteogenesis Imperfecta;Calcified Tissue International;2024-03-29

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