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Organization of the Care of Patients with Hyperphenylalaninemia in Slovakia
Authors: Strnová J.. Ürge O. 1 2; M. Beránková 1
Authors‘ workplace: Klinika pre deti a dorast A. Getlíka, SZU, NsP sv. Cyrila a Metoda, Bratislava1 prednostka doc. MUDr. K. Furková, CSc. Klinika laboratórnej medicíny, FNsP akademika L. Dérera, Bratislava2 prednosta prof. MUDr. RNDr. G. Kováč, CSc., MBA
Published in: Čes-slov Pediat 2003; (7): 421-422.
Category:
Overview
The authors describe organization of the care of patients suffering from hyperphenylalaninemia in Slovakia.The paper analyzes the method of active search for this hereditary metabolic disorder from the beginning to thepresent time and how the long-term complex care of the patients with hyperphenylalaninemia is provided.
Key words:
hyperphenylalaninemia, screening, complex care
Labels
Neonatology Paediatrics General practitioner for children and adolescents
Article was published inCzech-Slovak Pediatrics
2003 Issue 7-
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Most read in this issue- MCAD Deficiency - Our Experience with Four Symptomatic Patients
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- Tandem Mass Spectrometry - The Future of Newborn Screening of Inborn Errors of Metabolism
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