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phenylketonuria
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Petr Chrastina
External person at First Faculty of Medicine
40 publications
Publications
publication
Extremely low birthweight neonates with phenylketonuria require special dietary management
2021 |
First Faculty of Medicine, Central Library of Charles University
publication
Epidemiology of rare diseases detected by newborn screening in the Czech Republic
2019 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Newborn screening of inherited metabolic diseases in the Czech Republic
+1
2018 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Results of expanded newborn screening in the Czech Republic
2014 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Neonatal screening in the Czech Republic
2010 |
First Faculty of Medicine, Third Faculty of Medicine
publication
První český pacient s deficitem aminoacylázy 1
2023 |
First Faculty of Medicine
publication
The role of ERNDIM diagnostic proficiency schemes in improving the quality of diagnostic testing for inherited metabolic diseases
2022 |
First Faculty of Medicine
publication
X-linked adrenoleukodystrophy: phenotype-genotype correlation in hemizygous males and heterozygous females with ABCD1 mutations
2021 |
First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University
publication
Impact of newborn screening and early dietary management on clinical outcome of patients with long chain 3-hydroxyacyl-coa dehydrogenase deficiency and medium chain acyl-coa dehydrogenase deficiency-a retrospective nationwide study
2021 |
First Faculty of Medicine, Third Faculty of Medicine, Faculty of Mathematics and Physics
publication
Newborn screening for homocystinurias: Recent recommendations versus current practice
2019 |
First Faculty of Medicine, Faculty of Mathematics and Physics
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