Phenylketonuria - A Medical Dictionary, Bibliography, and by Icon Health Publications

By Icon Health Publications

This can be a 3-in-1 reference booklet. It offers a whole scientific dictionary overlaying thousands of phrases and expressions with regards to phenylketonuria. It additionally provides vast lists of bibliographic citations. ultimately, it offers details to clients on find out how to replace their wisdom utilizing a variety of web assets. The ebook is designed for physicians, scientific scholars getting ready for Board examinations, scientific researchers, and sufferers who are looking to familiarize yourself with examine devoted to phenylketonuria. in the event that your time is effective, this ebook is for you. First, you won't waste time looking out the web whereas lacking loads of proper details. moment, the publication additionally saves you time indexing and defining entries. ultimately, you won't waste time and cash printing 1000s of websites.

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Cmd=Retrieve&db=PubMed&list_ uids=11587123&dopt=Abstract • Associations between phenylalanine-to-tyrosine ratios and performance on tests of neuropsychological function in adolescents treated early and continuously for phenylketonuria. Author(s): Luciana M, Sullivan J, Nelson CA. Source: Child Development. 2001 November-December; 72(6): 1637-52. cmd=Retrieve&db=PubMed&list_ uids=11768137&dopt=Abstract • Barriers to successful dietary control among pregnant women with phenylketonuria. Author(s): Brown AS, Fernhoff PM, Waisbren SE, Frazier DM, Singh R, Rohr F, Morris JM, Kenneson A, MacDonald P, Gwinn M, Honein M, Rasmussen SA.

Source: Journal of Pediatric Psychology. 2001 December; 26(8): 477-84. cmd=Retrieve&db=PubMed&list_ uids=11700332&dopt=Abstract • Evaluation of 6-year application of the enzymatic colorimetric phenylalanine assay in the setting of neonatal screening for phenylketonuria. Author(s): Schulze A, Mayatepek E, Hoffmann GF. Source: Clinica Chimica Acta; International Journal of Clinical Chemistry. 2002 March; 317(1-2): 27-37. cmd=Retrieve&db=PubMed&list_ uids=11814455&dopt=Abstract Studies 37 • Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuria.

Cmd=Retrieve&db=PubMed&list_ uids=12504428&dopt=Abstract • Different phenotypic manifestations associated with identical phenylketonuria genotypes in two Spanish families. Author(s): Perez B, Desviat LR, Garcia MJ, Ugarte M. Source: Journal of Inherited Metabolic Disease. 1994; 17(3): 377-8. cmd=Retrieve&db=PubMed&list_ uids=7807962&dopt=Abstract • Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH gene. Author(s): Gizewska M, Cabalska B, Cyrytowski L, Nowacki P, Zekanowski C, Walczak M, Jozwiak I, Koziarska D.

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