Osteogenesis Imperfecta and hearing loss in the paediatric population
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference17 articles.
1. Osteogenesis imperfecta;Forlino JM;Lancet,2016
2. Management of osteogenesis imperfecta at the Chris Hani Baragwanath hospital;Oduah;SA Orthop J,2017
3. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J. Med. Genet.,1979
4. New perspectives on osteogenesis imperfecta;Forlino;Nat. Rev. Endocrinol.,2011
5. Osteogenesis imperfecta: phenotypic and intraoperative findings observed in patients treated surgically at the world hearing centre;Skarżyński;J Int Adv Otol,2018
Cited by 4 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. Annual hearing screening in children with osteogenesis imperfecta: Results from the first five years in glasgow;International Journal of Pediatric Otorhinolaryngology;2024-11
2. Characterization of hearing loss in pediatric patients with osteogenesis imperfecta;International Journal of Pediatric Otorhinolaryngology;2024-08
3. A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies;JBMR Plus;2024-03-04
4. The International Standard Set of Outcome Measures for the Assessment of Hearing in People with Osteogenesis Imperfecta;Otology & Neurotology;2023-06-16
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