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Pediatric Hematology and Oncology|August 28, 2010
Language skills in a child with Leber hereditary optic neuropathy following intrathecal chemotherapy for acute lymphoblastic leukemiaFiona M Lewis, David J Coman, Bruce E Murdoch
JIMD Reports|February 23, 2013
Differential phonological awareness skills in children with classic galactosemia: a descriptive study of four casesFiona M Lewis, David J Coman, Maryann Syrmis, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|July 11, 2013
Charting a seven-year trajectory of language outcomes for a child with galactosemiaFiona M Lewis, David J Coman, Maryann Syrmis, et al.
Developmental Neurorehabilitation|January 3, 2013
Pre-linguistic communication skill development in an infant with a diagnosis of galactosaemiaFiona M Lewis, David J Coman, Sarah Kilcoyne, et al.
The Journal of Pediatrics|April 16, 2008
Enzyme replacement therapy for mucopolysaccharidoses: opinions of patients and familiesDavid J Coman, Ian M Hayes, Veronica Collins, et al.
JIMD Reports|February 23, 2013
Enzyme replacement therapy and extended newborn screening for mucopolysaccharidoses: opinions of treating physiciansDavid J Coman, Ian M Hayes, Veronica Collins, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|November 5, 2013
Fumarase deficiency in dichorionic diamniotic twinsSimone Tregoning, Wendy Salter, David R Thorburn, et al.
Pediatric Research|December 3, 2009
Galactosemia, a single gene disorder with epigenetic consequencesDavid J Coman, David W Murray, Jennifer C Byrne, et al.
Journal of Paediatrics and Child Health|May 23, 2006
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndromeDavid J Coman, K G Sinclair, C J Burke, et al.
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