Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dóra, Becsei"'
Autor:
Dóra Becsei, Erika Kiss, Ildikó Szatmári, András Arató, György Reusz, Attila J. Szabó, János Bókay, Petra Zsidegh
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 32, Iss , Pp 100897- (2022)
Background: Patients with phenylketonuria (PKU) must maintain a lifelong natural protein-restricted diet to prevent neuro-cognitive damage. Early diagnosis is established with newborn screening, with diet subsequently controlled by regular phenylalan
Externí odkaz:
https://doaj.org/article/cbab2b25d772421bae68fa62fa968aa9
Autor:
Dóra Becsei, Réka Hiripi, Erika Kiss, Ildiko Szatmári, András Arató, György Reusz, Attila J. Szabó, János Bókay, Petra Zsidegh
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100823- (2021)
Background: Phenylketonuria (PKU) is an inherited error of metabolism, screened at 48–72 h of life since 1975 in Hungary. The patients have to keep a strict lifelong protein-restricted diet, resulting in PKU and its treatment can lead to social and
Externí odkaz:
https://doaj.org/article/c86b781c43d54dd8be711f5703206934
Autor:
Petra Zsidegh, Dóra Becsei, E. Kiss, János Bókay, Attila Szabo, Ildikó Szatmári, György Reusz, Réka Hiripi, András Arató
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss, Pp 100823-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Background Phenylketonuria (PKU) is an inherited error of metabolism, screened at 48–72 h of life since 1975 in Hungary. The patients have to keep a strict lifelong protein-restricted diet, resulting in PKU and its treatment can lead to social and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e53ae522ab7b57fcb8bad2598ad1e5
https://doi.org/10.1016/j.ymgmr.2021.100823
https://doi.org/10.1016/j.ymgmr.2021.100823
Publikováno v:
Orvosképzés; 2020, Issue 3, p532-538, 7p