Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Boris Privrodski"'
Publikováno v:
Balkan Medical Journal, Vol 36, Iss 1, Pp 60-61 (2019)
Externí odkaz:
https://doaj.org/article/5090011239df41498167a7ccd9e0e19a
Autor:
Ivana Kavecan, Milan Obrenovic, Jadranka Jovanovic Privrodski, Boris Privrodski, Mihajlo Jeckovic
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 6, Pp 445-446 (2018)
Externí odkaz:
https://doaj.org/article/979f1005b8734810840205fed8d53dd9
Autor:
Boris Privrodski, Tatjana Redzek-Mudrinic, Ivana Kavecan, Milan Obrenovic, Jadranka Jovanovic
Publikováno v:
Medical review. 70:411-415
Introduction. Phenylketonuria is an inborn disorder of metabolism, a rare, hereditary disease caused by deficiency of phenylalanine hydroxylase enzyme necessary for conversion of phenylalanine into tyrosine. The aim of this study is to determine the
Autor:
Jadranka Jovanovic Privrodski, Ivana Kavecan, Tatjana Redzek Mudrinic, Milan Obrenovic, Boris Privrodski
Publikováno v:
Endocrine Abstracts.
Autor:
Jadranka Jovanovic Privrodski, Boris Privrodski, Ivana Kavecan, Radojica Savic, Tatjana Redzek Mudrinic, Milan Obrenovic
Publikováno v:
Journal of cutaneous medicine and surgery. 23(2)
Publikováno v:
Balkan Medical Journal
Balkan Medical Journal, Vol 36, Iss 1, Pp 60-61 (2019)
Balkan Medical Journal, Vol 36, Iss 1, Pp 60-61 (2019)
Publikováno v:
Endocrine Abstracts.
Autor:
Boris Privrodski, Ivana Kavecan, Milan Obrenovic, Jadranka Jovanovic Privrodski, Mihajlo Jeckovic
Publikováno v:
Balkan Medical Journal, Vol 35, Iss 6, Pp 445-446 (2018)
Balkan Medical Journal
Balkan Medical Journal