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Journal of Neurosurgery|May 10, 2008
Presurgical and postsurgical assessment of the neurodevelopment of infants with single-suture craniosynostosis: comparison with controlsJacqueline R Starr, Kathleen A Kapp-Simon, Yona Keich Cloonan, et al.The Journal of Craniofacial Surgery|July 16, 2013
Laypersons' ratings of appearance in children with and without single-suture craniosynostosisBrent R Collett, Kristen E Gray, Kathleen A Kapp-Simon, et al.Neurosurgery|September 18, 2008
New severity indices for quantifying single-suture metopic craniosynostosisSalvador Ruiz-Correa, Jacqueline R Starr, H Jill Lin, et al.Neurosurgery|July 21, 2010
Little evidence of association between severity of trigonocephaly and cognitive development in infants with single-suture metopic synostosisJacqueline R Starr, H Jill Lin, Salvador Ruiz-Correa, et al.Paediatric Anaesthesia|April 17, 2012
Duration of exposure to cranial vault surgery: associations with neurodevelopment among children with single-suture craniosynostosisHeather L Naumann, Charles M Haberkern, Kristen E Pietila, et al.Birth Defects Research|March 31, 2019
Evaluation of prenatal diabetes mellitus and other risk factors for craniofacial microsomiaBabette Siebold, Carrie L Heike, Brian G Leroux, et al.The Journal of Pediatrics|April 25, 2018
Neurodevelopment of Infants with and without Craniofacial MicrosomiaMatthew L Speltz, Kathleen A Kapp-Simon, Alexis L Johns, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|November 29, 2016
Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical researchCarrie L Heike, Erin Wallace, Matthew L Speltz, et al.Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|September 28, 2007
Memory and response inhibition in young children with single-suture craniosynostosisKaren Toth, Brent Collett, Kathleen A Kapp-Simon, et al.American Journal of Medical Genetics. Part A|August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosisHeather C Mefford, Neil Shafer, Francesca Antonacci, et al.Pageof 8