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Journal of Pediatric Ophthalmology and Strabismus|October 6, 2000
Ocular findings in glutaric aciduria type 1N A Kafil-Hussain, A Monavari, R Bowell, et al.Irish Medical Journal|February 6, 2019
Hyperammonaemia in Neonates and Young Children: Potential Metabolic Causes, Diagnostic Approaches and Clinical ConsequencesS Giva, J Finnegan, P Ihidero, et al.Irish Medical Journal|April 21, 2020
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) in the Irish Paediatric PopulationZ Mesbah, K Sing Ho, P Fitzsimons, et al.Irish Medical Journal|July 1, 2017
Rotavirus Gastroenteritis is Associated with Increased Morbidity and Mortality in Children with Inherited Metabolic DisordersA Smith, M Mannion, P O'Reilly, et al.Journal of Inherited Metabolic Disease|October 27, 2004
Glutaric aciduria type I: outcome in the Republic of IrelandE R Naughten, P D Mayne, A A Monavari, et al.JIMD Reports|June 27, 2019
Ten-year retrospective review (2003-2013) of 56 inpatient admissions to stabilize elevated phenylalanine levelsAnne Clark, Christine Merrigan, Ellen Crushell, et al.European Journal of Pediatrics|November 14, 2022
An approach to recognising and identifying metabolic presentations in the paediatric Irish Traveller populationE B Forman, S A Lynch, I Knerr, et al.European Journal of Pediatrics|November 26, 2016
A review of anaesthetic outcomes in patients with genetically confirmed mitochondrial disordersA Smith, E Dunne, M Mannion, et al.Irish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.Journal of Inherited Metabolic Disease|August 9, 2012
Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatmentK P Coss, P P Doran, C Owoeye, et al.Pageof 3