Severe osteogenesis imperfecta Type-III and its challenging treatment in newborn and preschool children. A systematic review-Reference-Cited by-同舟云学术

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Severe osteogenesis imperfecta Type-III and its challenging treatment in newborn and preschool children. A systematic review

Published:2015-08 Issue:8 Volume:46 Page:1440-1446
ISSN:0020-1383
Container-title:Injury
language:en
Short-container-title:Injury

Author:

Sinikumpu Juha-Jaakko,Ojaniemi Marja,Lehenkari Petri,Serlo Willy

Funder

Finnish Medical Foundation

The Emil Aaltonen Foundation

Publisher

Elsevier BV

Subject

Orthopedics and Sports Medicine,Emergency Medicine

Reference51 articles.

1. Skeletal clinical characteristics of osteogenesis imperfecta caused by haploinsufficiency mutations in COL1A1;Amor;J Bone Miner Res,2013

2. Osteogenesis imperfecta in childhood: treatment strategies;Engelbert;Arch Phys Med Rehabil,1998

3. Osteogenesis imperfecta: a genetic, radiological, and epidemiological study;Andersen;Clin Genet,1989

4. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J Med Genet,1979

5. Hearing loss in patients with osteogenesis imperfecta. A clinical and audiological study of 201 patients;Pedersen;Scand Audiol,1984

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1. A novel sliding double flexible intramedullary nail technique for the management of lower extremity long bone fractures and deformities in osteogenesis imperfecta;Journal of Pediatric Orthopaedics B;2024-03-20

2. Osteogénesis imperfecta tipo III con presentación inusual;Revista Repertorio de Medicina y Cirugía;2023-10-18

3. The patient-related factors in revision procedures on tibia of patients with osteogenesis imperfecta treated with the Peter-Williams nail;Journal of Orthopaedic Surgery and Research;2023-07-26

4. Fixation techniques in lower extremity correction osteotomies and fractures in mild-to-severe osteogenesis imperfecta patients: evaluation of the results and complications;Journal of Orthopaedic Surgery and Research;2023-06-16

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