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	1.	Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management. [electronic resource] by Monavari, A A Naughten, E R Producer: 20000301 In: Archives of disease in childhood vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Late-infantile 3-methylcrotonyl-CoA carboxylase deficiency presenting as global developmental delay. [electronic resource] by Yap, S Monavari, A A Thornton, P Naughten, E Producer: 19980611 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Type 1 Tyrosinaemia. [electronic resource] by Mannion, M A Smith, A Mayne, P Monavari, A A Producer: 20181022 In: Irish medical journal vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	4.	Long chain fatty acid oxidation defects in children: importance of detection and treatment options. [electronic resource] by Hayes, B Lynch, B O'Keefe, M Monavari, A A Treacy, E P Producer: 20080118 In: Irish journal of medical science vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Should children with inherited metabolic disorders receive varicella vaccination? [electronic resource] by Varghese, M Cafferkey, M O'Regan, M Monavari, A A Treacy, E P Producer: 20110128 In: Archives of disease in childhood vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) in the Irish Paediatric Population. [electronic resource] by Mesbah, Z Sing Ho, K Fitzsimons, P Monavari, A A Mayne, P D Crushell, E Producer: 20200709 In: Irish medical journal vol. 112 Availability: No items available. Save to lists Add to cart (remove)
	7.	Glutaric aciduria type I: outcome in the Republic of Ireland. [electronic resource] by Naughten, E R Mayne, P D Monavari, A A Goodman, S I Sulaiman, G Croke, D T Producer: 20050505 In: Journal of inherited metabolic disease vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Glutaric aciduria and suspected child abuse. [electronic resource] by Morris, A A Hoffmann, G F Naughten, E R Monavari, A A Collins, J E Leonard, J V Producer: 19991013 In: Archives of disease in childhood vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A review of anaesthetic outcomes in patients with genetically confirmed mitochondrial disorders. [electronic resource] by Smith, A Dunne, E Mannion, M O'Connor, C Knerr, I Monavari, A A Hughes, J Eustace, N Crushell, E Producer: 20170808 In: European journal of pediatrics vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mitochondrial cytopathies, phenotypic heterogeneity and a high incidence. [electronic resource] by Ryan, E King, M D Rustin, P Mayne, P D Brown, G K Monavari, A A Walsh, R Treacy, E P Producer: 20070104 In: Irish medical journal vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	11.	Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatment. [electronic resource] by Coss, K P Doran, P P Owoeye, C Codd, M B Hamid, N Mayne, P D Crushell, E Knerr, I Monavari, A A Treacy, E P Producer: 20130924 In: Journal of inherited metabolic disease vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Pregnancy management and outcome in patients with four different tetrahydrobiopterin disorders. [electronic resource] by Kuseyri, O Weissbach, A Bruggemann, N Klein, C Giżewska, M Karall, D Scholl-Bürgi, S Romanowska, H Krzywińska-Zdeb, E Monavari, A A Knerr, I Yapıcı, Z Leuzzi, V Opladen, T Producer: 20191107 In: Journal of inherited metabolic disease vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARS. [electronic resource] by Casey, Jillian P Slattery, Suzanne Cotter, Melanie Monavari, A A Knerr, Ina Hughes, Joanne Treacy, Eileen P Devaney, Deirdre McDermott, Michael Laffan, Eoghan Wong, Derek Lynch, Sally Ann Bourke, Billy Crushell, Ellen Producer: 20160920 In: Journal of inherited metabolic disease vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. [electronic resource] by Hoffmann, G F Athanassopoulos, S Burlina, A B Duran, M de Klerk, J B Lehnert, W Leonard, J V Monavari, A A Müller, E Muntau, A C Naughten, E R Plecko-Starting, B Superti-Furga, A Zschocke, J Christensen, E Producer: 19970114 In: Neuropediatrics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)