Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Journal of Medical Biochemistry|March 31, 2017
Different Viewpoints: International Perspectives on Newborn ScreeningRodney J PollittActa Paediatrica (Oslo, Norway : 1992)|July 22, 2010
New technologies extend the scope of newborn blood-spot screening, but old problems remain unresolvedRodney J PollittApplied Health Economics and Health Policy|November 4, 2010
Cost effectiveness of establishing a neonatal screening programme for phenylketonuria in LibyaErikas Sladkevicius, Rodney J Pollitt, Ali Mgadmi, et al.Developmental Medicine and Child Neurology|September 8, 2011
Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiencyRuchi Sharma, Mark J Sharrard, Daniel J Connolly, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 18, 2006
The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an updateScott D Grosse, Muin J Khoury, Carol L Greene, et al.JIMD Reports|February 23, 2013
Riboflavin-responsive trimethylaminuria in a patient with homocystinuria on betaine therapyNigel J Manning, Elizabeth K Allen, Richard J Kirk, et al.Developmental Medicine and Child Neurology|January 27, 2007
Magnetic resonance spectroscopy changes following haemopoietic stem cell transplantation in children with cerebral adrenoleukodystrophyDaniel J Warren, Daniel J A Connolly, Iain D Wilkinson, et al.American Journal of Medical Genetics|September 5, 2002
Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathyAnne-Marie Lamhonwah, Simon E Olpin, Rodney J Pollitt, et al.Gastroenterology|February 24, 2010
Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)Jane Louise Hartley, Nicholas C Zachos, Ban Dawood, et al.The New England Journal of Medicine|November 13, 2014
Monocarboxylate transporter 1 deficiency and ketone utilizationPeter M van Hasselt, Sacha Ferdinandusse, Glen R Monroe, et al.Pageof 1