Joanna Taybert
Warsaw, MZ 01211, Poland
Last Updated: 09/26/2026
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Found 7 publications
Medium-chain Acyl-CoA Dehydrogenase Deficiency Identified by MS/MS Newborn Screening Challenges.
Journal: Journal of mother and child
Published: July 18, 2025
Molecular Background and Disease Prevalence of Biotinidase Deficiency in a Polish Population-Data Based on the National Newborn Screening Programme.
Journal: Genes
Published: April 10, 2022
Treatment of classic phenylketonuria in Poland in the years 2009-2015 based on the database of the Polish National Health Fund.
Journal: Pediatric endocrinology, diabetes, and metabolism
Published: September 09, 2020
Medical care of patients with disorders of aromatic amino acid metabolism: a report based on the Polish National Health Fund data records.
Journal: Pediatric endocrinology, diabetes, and metabolism
Published: February 22, 2019
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome.
Journal: Journal of inherited metabolic disease
Published: February 24, 2016
Clinical and molecular characteristics of two transaldolase-deficient patients.
Journal: European journal of pediatrics
Published: August 01, 2013
Showing 1-7 of 7
Last Updated: 09/26/2026