Topic Metabolic diseases in children
REVIEW PAPER
Modification of gut microbiota in the treatment of childhood obesity
Pediatr Pol 2026;62(2):154-160
ORIGINAL PAPER
Integrating diet and exercise to effectively reduce fat mass in children with obesity during weight reduction program
Pediatr Pol 2026;62(2):140-145
ORIGINAL PAPER
Analysis of selected biomarkers of obesity-related complications in the paediatric population
Oliwia Piaskowska, Anna Jakubowska, Agnieszka Matera-Witkiewicz, Mateusz Sikora, Magdalena Krupińska, Agnieszka Bargenda-Lange, Anna Medyńska, Katarzyna Zatońska, Katarzyna Połtyn-Zaradna, Tomasz Zatoński, Katarzyna Kiliś-Pstrusińska
Pediatr Pol 2026;62(1):36-42
Editor's Choice
REVIEW PAPER
A brief guide to the genetics of autism spectrum disorders
Pediatr Pol 2026;62(1):57-67
Editor's Choice
ORIGINAL PAPER
Long-term trends in physical fitness and body mass among 10- year-olds in Gdansk: findings from a 12-year intervention programme
Magdalena Dettlaff-Dunowska, Aleksandra Lemanowicz-Kustra, Michał Brzeziński, Oliver Sowulewski, Katarzyna Plata-Nazar, Agnieszka Szlagatys-Sidorkiewicz
Pediatr Pol 2026;62(1):23-28
ORIGINAL PAPER
Assessment of the nutritional status of children in the Lodzkie Voivodeship – “Growing Healthy” Project, pilot study
Bogumiła Alicja Górczewska, Elżbieta Woźniak, Jakub Krzysztof Nowicki, Dominika Matczak, Agata Petrovic, Paulina Adamiecka, Ewa Rychlowska, Żaneta Lewandowska, Agnieszka Byrwa-Sztaba, Elżbieta Jakubowska-Pietkiewicz
Pediatr Pol 2025;61(4):332-339
CASE REPORT
Menkes disease – a rare disorder requiring interdisciplinary management
Magdalena Jaworek, Przemysław Hałubiec, Magdalena Janeczko, Małgorzata Steczkowska, Andrzej Jaworek, Sławomir Kroczka, Anna Wojas-Pelc, Przemko Kwinta
Pediatr Pol 2025;61(4):370-375
REVIEW PAPER
The usability of bioelectrical impedance analysis in overweight and obese children
Pediatr Pol 2025;61(3):253-259
ORIGINAL PAPER
Assessment of nutritional status and the occurrence of complications in children with obesity based on its severity
Pediatr Pol 2025;61(2):135-140
ORIGINAL PAPER
Evaluation of the levels of kidney injury molecule-1 and cystatin C as early biomarkers for prediction of acute kidney injury complications in paediatric male patients – a case-control study
Pediatr Pol 2025;61(1):38-51
ORIGINAL PAPER
The continuous glucose monitoring system correlates poorly with the glucose infusion rate
Pediatr Pol 2025;61(1):23-28
REVIEW PAPER
Inherited glycosylphosphatidylinositol deficiency disorders: a new group of inherited metabolic disorders
Michał Patalan, Alicja Leśniak, Justyna Paprocka, Agnieszka Zubkiewicz-Kucharska, Kaja Giżewska-Kacprzak, Marta Glińska, Lidia Babiak-Choroszczak, Maria Giżewska, Robert Śmigiel
Pediatr Pol 2024;99(4):329-334
REVIEW PAPER
A genetic disease under the multiform mask – infantile-onset of Pompe disease
Pediatr Pol 2024;99(3):218-224
CASE REPORT
MYT1L mutation in a patient with severe early-onset obesity and intellectual disability
Pediatr Pol 2024;99(2):164-166
CASE REPORT
Bilateral infectious urolithiasis as a risk factor for acute kidney failure in a 3-year-old boy
Karina Madej-Świątkowska, Magdalena Błasiak, Monika Miklaszewska, Andrzej Haliński, Adam Haliński, Katarzyna Zachwieja, Anna Moczulska, Dorota Drożdż
Pediatr Pol 2024;99(2):149-152
ORIGINAL PAPER
Feeding problems, eating disorders, and nutritional status of Polish children and adolescents with neurodevelopmental disorders – a cross-sectional pilot study
Martina Grot, Agnieszka Białek-Dratwa, Karolina Krupa-Kotara, Mateusz Grajek, Maciej Nigowski, Elżbieta Szczepańska, Oskar Kowalski
Pediatr Pol 2024;99(1):37-45
ORIGINAL PAPER
Association between the metabolic profile of urolithiasis in children with idiopathic hypercalciuria and the composition of the stone assessed by infrared spectroscopy
Małgorzata Placzyńska, Joanna Milart, Arkadiusz Lubas, Joanna Samotyjek, Beata Jurkiewicz, Bolesław Kalicki, Katarzyna Jobs
Pediatr Pol 2023;98(4):271-277
ORIGINAL PAPER
A recent overview of non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: pathophysiology, recognition, and management
Pediatr Pol 2023;98(4):307-319
CASE REPORT
Accidentally detected nephrocalcinosis in a boy with a homozygous R396W mutation in the CYP24A1 gene – 7-year follow-up
Jakub Krzysztof Nowicki, Anna Maćkowska, Małgorzata Rychwalska, Marcin Zaniew, Elżbieta Jakubowska-Pietkiewicz
Pediatr Pol 2023;98(4):351-361
REVIEW PAPER
Effect of vitamin D level on COVID-19 and the risk of complications in children
Pediatr Pol 2023;98(2):140-144
CASE REPORT
Deletion of the RNF6 gene in a patient with epileptic encephalopathy – a case report and literature review
Pediatr Pol 2022;97(3):264-268
CASE REPORT
From the hypertransaminasemia symptoms to the recognition of late-onset Pompe disease in a 12-year-old boy
Pediatr Pol 2021;96(3):220-222
ORIGINAL PAPER
The amount of monounsaturated, polyunsaturated, and saturated fatty acids in the diet of fifteen-year-olds boys and girls in correlation with body mass index values
Pediatr Pol 2021;96(1):38-46
CASE REPORT
Gordon syndrome in an 11-year-old boy: long-term follow-up
Andrzej Badeński, Marta Badeńska, Omar Bjanid, Justyna Czubilińska-Łada, Aleksandra Gliwińska, Anna Bogdał, Olga Kupczyk, Maria Szczepańska
Pediatr Pol 2020;95(3):184-190
ORIGINAL PAPER
Skeletal complications in the course of neurofibromatosis in children
Pediatr Pol 2019;94(3):151-157
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