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Journal of Paediatrics and Child Health|October 25, 2011
Extended newborn screening: an update for the general paediatricianDavid Coman, Kaustuv BhattacharyaChild Neurology Open|May 16, 2017
De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin SyndromeAnand Ramineni, David ComanClinics and Practice|October 26, 2016
Persistent Hyperinsulinism in Kabuki Syndrome 2: Case Report and Literature ReviewHobia Gole, Raymond Chuk, David ComanDNA Repair|October 28, 2025
Lets talk about ataxia-telangiectasia: Meeting report of the AT clinical research conference June 2025David Coman, Penny Jeggo, Martin LavinClinics and Practice|October 3, 2018
<i>SYNE1</i>-related autosomal recessive cerebellar ataxia, congenital cerebellar hypoplasia, and cognitive impairmentLauren Swan, John Cardinal, David ComanJournal of Paediatrics and Child Health|December 3, 2014
Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical featureShekeeb S Mohammad, David Coman, Sophie CalvertClinical Nutrition (Edinburgh, Scotland)|July 22, 2008
New indications and controversies in arginine therapyDavid Coman, Joy Yaplito-Lee, Avihu BonehClinics and Practice|August 4, 2015
Septic Arthritis of the Temporomandibular Joint in an InfantRaymond Chuk, John Arvier, Barbara Laing, et al.Child Neurology Open|May 16, 2017
Pediatric Hereditary Neuralgic Amyotrophy: Successful Treatment With Intravenous Immunoglobulin and Insights Into <i>SEPT9</i> PathogenesisRaymond Chuk, Megan Sheppard, Geoff Wallace, et al.Clinical Case Reports|March 9, 2019
A novel familial 9q31.2q32 microdeletion: Muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short statureAnand K Ramineni, Trent Burgess, Penny Cruickshanks, et al.Pageof 7