Long-term follow-up of patients with phenylketonuria treated with tetrahydrobiopterin: a seven years experience

BACKGROUND: Phenylketonuria (PKU) is an autosomal recessive disorder caused by the deficiency of phenylalanine hydroxylase that catalyzes the conversion of phenylalanine to tyrosine, using tetrahydrobiopterin (BH4) as coenzyme. Besides dietary phenylalanine restriction, new therapeutic options are e...

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Detalles Bibliográficos
Autores principales: Scala, Iris, Concolino, Daniela, Casa, Roberto Della, Nastasi, Anna, Ungaro, Carla, Paladino, Serena, Capaldo, Brunella, Ruoppolo, Margherita, Daniele, Aurora, Bonapace, Giuseppe, Strisciuglio, Pietro, Parenti, Giancarlo, Andria, Generoso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351928/
https://www.ncbi.nlm.nih.gov/pubmed/25757997
http://dx.doi.org/10.1186/s13023-015-0227-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351928/
https://www.ncbi.nlm.nih.gov/pubmed/25757997
http://dx.doi.org/10.1186/s13023-015-0227-8

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