Bozena Didycz

Krakow, MA, Poland

Last Updated: 09/26/2026

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Found 17 publications

Professional activity, gender and disease-related emotions: The impact on parents' experiences in caring for children with phenylketonuria.

Professional activity, gender and disease-related emotions: The impact on parents' experiences in caring for children with phenylketonuria.

Journal: Molecular genetics and metabolism reports

Published: May 17, 2023

Phenylketonuria Patients' and Their Caregivers' Perception of the Pandemic Lockdown: The Results of a National Online Survey.

Phenylketonuria Patients' and Their Caregivers' Perception of the Pandemic Lockdown: The Results of a National Online Survey.

Journal: Children (Basel, Switzerland)

Published: November 22, 2021

Management precautions for risk of obesity are necessary among infants with PKU carrying the rs113883650 variant of the LAT1 gene: A cross-sectional study.

Management precautions for risk of obesity are necessary among infants with PKU carrying the rs113883650 variant of the LAT1 gene: A cross-sectional study.

Journal: PloS one

Published: August 21, 2021

The Impact of the First 2020 COVID-19 Lockdown on the Metabolic Control of Patients with Phenylketonuria.

The Impact of the First 2020 COVID-19 Lockdown on the Metabolic Control of Patients with Phenylketonuria.

Journal: Nutrients

Published: April 30, 2021

The Impact of the COVID-19 Pandemic on the Perception of Health and Treatment-Related Issues among Patients with Phenylketonuria in Poland-The Results of a National Online Survey.

The Impact of the COVID-19 Pandemic on the Perception of Health and Treatment-Related Issues among Patients with Phenylketonuria in Poland-The Results of a National Online Survey.

Journal: International journal of environmental research and public health

Published: March 29, 2021

Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria.

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

Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?

Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?

Journal: Nutrients

Published: September 15, 2019

Weaning practices in phenylketonuria vary between health professionals in Europe.

Weaning practices in phenylketonuria vary between health professionals in Europe.

Journal: Molecular genetics and metabolism reports

Published: October 12, 2018

Early feeding practices in infants with phenylketonuria across Europe.

Early feeding practices in infants with phenylketonuria across Europe.

Journal: Molecular genetics and metabolism reports

Published: June 07, 2018

Can untreated PKU patients escape from intellectual disability? A systematic review.

Can untreated PKU patients escape from intellectual disability? A systematic review.

Journal: Orphanet journal of rare diseases

Published: May 04, 2018

Blood phenylalanine instability strongly correlates with anxiety in phenylketonuria.

Blood phenylalanine instability strongly correlates with anxiety in phenylketonuria.

Journal: Molecular genetics and metabolism reports

Published: November 03, 2017

The Use of d2 and Benton Tests for Assessment of Attention Deficits and Visual Memory in Teenagers with Phenylketonuria.

The Use of d2 and Benton Tests for Assessment of Attention Deficits and Visual Memory in Teenagers with Phenylketonuria.

Journal: JIMD reports

Published: July 24, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026