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	1.	Clinical experience with intravenous Augmentin in the treatment of paediatric infections. [electronic resource] by Ploechl, E Huber, E G Producer: 19860725 In: The Journal of international medical research vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency. [electronic resource] by Ploechl, E Bachmann, C Colombo, J P Gibson, K M Producer: 19900305 In: Journal of inherited metabolic disease vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Late-onset ornithine transcarbamylase deficiency in two families with different mutations in the same codon. [electronic resource] by Ploechl, E Ploechl, W Stoeckler-Ipsiroglu, S Pokorny, H Wermuth, B Producer: 20010621 In: Clinical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Outcome of tyrosinaemia type III. [electronic resource] by Ellaway, C J Holme, E Standing, S Preece, M A Green, A Ploechl, E Ugarte, M Trefz, F K Leonard, J V Producer: 20020918 In: Journal of inherited metabolic disease vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria. [electronic resource] by Tomoeda, K Awata, H Matsuura, T Matsuda, I Ploechl, E Milovac, T Boneh, A Scott, C R Danks, D M Endo, F Producer: 20001228 In: Molecular genetics and metabolism vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)