An update of ophthalmic management in craniosynostosis
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology and Child Health
Reference60 articles.
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2. Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis;Wilkie;Pediatrics,2010
3. Syndromic craniosynostosis: from history to hydrogen bonds;Cunningham;Orthod Craniofac Res,2007
4. Focus session on the changing “epidemiology” of craniosynostosis (comparing two quinquennia: 1985-1989 and 2003-2007) and its impact on the daily clinical practice: a review from Necker Enfants Malades;Di Rocco;Childs Nerv Syst,2009
5. Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications;Lattanzi;Childs Nerv Syst,2012
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2. The Outcome of Inferior Oblique Myectomy for Apparent Inferior Oblique Overaction Associated with Craniosynostosis;Korean Journal of Ophthalmology;2024-08-05
3. Lacrimal Obstruction in Craniosynostosis: Anatomical and Genetic Risk Factors;Ophthalmic Plastic & Reconstructive Surgery;2024-05-09
4. Skeletal expansion via craniofacial distraction osteogenesis technique in syndromic craniosynostosis: impact on ophthalmic parameters;International Ophthalmology;2024-03-19
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