Joanna Zolkowska
Warsaw, MZ, Poland
Last Updated: 09/26/2026
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Found 8 publications
Comparison of phenylalanine tolerance in singleton and twin pregnancies in patients with phenylketonuria.
Journal: The Journal of international medical research
Published: September 23, 2020
Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria.
Journal: Molecular genetics and metabolism reports
Published: July 11, 2020
Diversity of phenylalanine tolerance in pregnant phenylketonuria patients homozygous for the p.R408W mutation: the need for improved understanding of phenylalanine homeostasis.
Journal: Journal of biological regulators and homeostatic agents
Published: March 25, 2019
Weaning practices in phenylketonuria vary between health professionals in Europe.
Journal: Molecular genetics and metabolism reports
Published: October 12, 2018
Low increase in phenylalanine tolerance during pregnancies in PKU woman with high prepregnancy BMI and postconceptional initiation of diet: A case report.
Journal: International journal of reproductive biomedicine
Published: August 12, 2018
Early feeding practices in infants with phenylketonuria across Europe.
Journal: Molecular genetics and metabolism reports
Published: June 07, 2018
Singleton and twin pregnancies of PKU patients - individual variability of phenylalanine tolerance: experience of a single treatment center (Preliminary report)
Journal: Developmental period medicine
Published: January 02, 2018
High plasma folate in patients with phenylketonuria
Journal: Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego
Published: May 04, 2016
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Last Updated: 09/26/2026