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Clinica Chimica Acta; International Journal of Clinical Chemistry|November 9, 2004
Determination of creatinine in urine by tandem mass spectrometryRenata Husková, Petr Chrastina, Tomás Adam, et al.
Drug Metabolism and Personalized Therapy|March 7, 2022
The markers of the organic acidemias and their ratios in healthy neonates in Serbian populationAnđelo Beletić, Aleksandra Tijanić, Petr Chrastina, et al.
Nucleosides, Nucleotides & Nucleic Acids|June 25, 2026
The impact of vitamin B12 deficiency on urinary profile of de novo purine synthesis intermediates: consequences of the methylfolate trapJakub Krijt, Václava Škopová, Jitka Sokolová, et al.
Journal of Inherited Metabolic Disease|May 13, 2022
The role of ERNDIM diagnostic proficiency schemes in improving the quality of diagnostic testing for inherited metabolic diseasesDéborah Mathis, Joanne Croft, Petr Chrastina, et al.
Casopis Lekaru Ceskych|December 2, 2010
[Clinical, biochemical and molecular characteristics in 11 Czech children with tyrosinemia type I]Alzbeta Vondrácková, Markéta Tesarová, Martin Magner, et al.
European Journal of Pediatrics|August 24, 2018
Neonatal screening in the Czech Republic: increased prevalence of selected diseases in low birthweight neonatesJan David, Petr Chrastina, Hana Vinohradska, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 21, 2021
Extremely low birthweight neonates with phenylketonuria require special dietary managementMarketa Zemanova, Petr Chrastina, Vaclav Sebron, et al.
Neuro Endocrinology Letters|September 10, 2021
X-linked adrenoleukodystrophy: phenotype-genotype correlation in hemizygous males and heterozygous females with ABCD1 mutationsMarketa Zemanova, Petr Chrastina, Lenka Dvorakova, et al.
Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquee, Nutrition Et Metabolisme|February 28, 2015
Carnitine supplementation alleviates lipid metabolism derangements and protects against oxidative stress in non-obese hereditary hypertriglyceridemic ratsMonika Cahova, Petr Chrastina, Hana Hansikova, et al.
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