Author:
Muntau Ania C.,Adams Darius J.,Bélanger-Quintana Amaya,Bushueva Tatiana V.,Cerone Roberto,Chien Yin-Hsiu,Chiesa Ana,Coşkun Turgay,de las Heras Javier,Feillet François,Katz Rachel,Lagler Florian,Piazzon Flavia,Rohr Fran,van Spronsen Francjan J.,Vargas Paula,Wilcox Gisela,Bhattacharya Kaustuv
Funder
BioMarin Pharmaceutical Inc
Nutricia
Vitaflo
BioMarin
Sanofi-Genzyme
Merck
Mead-Johnson
Genzyme
Merck-Serono
Danone
Alexion
Shire
Amicus Therapeutics
BioMarin Pharmaceutical, Inc
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference66 articles.
1. Phenylketonuria;Blau;Lancet,2010
2. Key European guidelines for the diagnosis and management of patients with phenylketonuria;van Spronsen;Lancet Diabetes Endocrinol.,2017
3. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014
4. Newborn PKU screening in Turkey: at present and organization for future;Ozalp;Turk. J. Pediatr.,2001
5. Detection of phenylketonuria by the newborn screening program in Thailand;Pangkanon;Southeast Asian J. Trop. Med. Public Health,2009
Cited by
47 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献