¿Qué debe saber el pediatra de las hiperfenilalaninemias?-Reference-Cited by-同舟云学术

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¿Qué debe saber el pediatra de las hiperfenilalaninemias?

Published:2015-05 Issue:3 Volume:86 Page:214-218
ISSN:0370-4106
Container-title:Revista Chilena de Pediatría
language:es
Short-container-title:Revista Chilena de Pediatría

Author:

Bravo Paulina,Raimann Erna,Cabello Juan Francisco,Arias Carolina,Peredo Pilar,Castro Gabriela,Hamilton Valerie,Campo Karen,Cornejo Verónica

Publisher

Sociedad Chilena de Pediatria

Subject

Pediatrics, Perinatology, and Child Health

Link

https://www.sciencedirect.com/science/article/pii/S0370410615000674/pdfft?isDTMRedir=true&download=true

Reference9 articles.

1. Past, present and future of newborn screening in Chile;Cornejo;J Inherit Metab Dis,2010

2. Phenylketonuria due to phenylalanine hydroxylase deficiency: An unfolding story. Medical Research Council Working Party on Phenylketonuria;BMJ,1993

3. Human phenylalanine hydroxilase mutations and hyperphenylaninemia phenotypes: A metanalysis of genotype-phenotype correlations;Kayaalp;Am J Hum Genet.,1997

4. Phenylketonuria;Blau;Lancet.,2010

5. Errores innatos del metabolismo;Colombo,2003

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