ARCHIVE
2/2025 vol. 100
Recommendations for the diagnosis of respiratory syncytial virus (RSV) infection in children. The Polish Society of Paediatrics and the National Paediatric Consultant’s recommendations
August Wrotek, Teresa Jackowska, Artur Mazur, Tomasz Szczepański, Ewa Toporowska-Kowalska, Łukasz Dembiński, Iwona Beń-Skowronek, Anna Medyńska, Katarzyna Plata-Nazar, Jan Styczyński, Piotr Hartmann, Tomasz Jarmoliński, Anna Turska-Kmieć, Jarosław Peregud-Pogorzelski
Pediatr Pol 2025;100(2):117-128
ORIGINAL PAPER
A retrospective analysis of newborns with congenital teratomas
Małgorzata Kamińska, Aleksandra Bartoś, Maria Marta Orzeł, Beata Borek-Dzięcioł, Katarzyna Gutowska-Malina, Joanna Schreiber-Zamora, Bożena Kociszewska-Najman
Pediatr Pol 2025;100(2):129-134
ORIGINAL PAPER
Assessment of nutritional status and the occurrence of complications in children with obesity based on its severity
Pediatr Pol 2025;100(2):135-140
ORIGINAL PAPER
The clinical course of varicella and herpes zoster in children with inflammatory bowel disease – a prospective study
Magdalena Chazan, Ewa Talarek, Kinga Kowalska-Duplaga, Katarzyna Kamila Bąk-Drabik, Mariusz Szczepanik, Sabina Więcek, Marcin Banasiuk, Andrzej Radzikowski, Aleksandra Banaszkiewicz
Pediatr Pol 2025;100(2):141-150
ORIGINAL PAPER
Nurses’ knowledge of paediatric gastrostomy care
Beata Winnicka, Łukasz Dembiński, Marcin Banasiuk, Marcin Dziekiewicz, Izabella Łazowska-Przeorek, Katarzyna Karolewska-Bochenek, Aleksandra Banaszkiewicz
Pediatr Pol 2025;100(2):151-156
REVIEW PAPER
Amplatzer occluders – a breakthrough in the interventional treatment of congenital heart defects. 27 years of experience
Pediatr Pol 2025;100(2):157-160
REVIEW PAPER
Reviving hope – the journey of diagnosing and treating Guillain-Barré syndrome
Anna Oleszczuk, Julia Kozieł, Szymon Kosmala, Noemi Kufrejska, Paweł Hawranik, Katarzyna Jurkiewicz, Marcelina Kurek, Magdalena Chrościńska-Krawczyk
Pediatr Pol 2025;100(2):166-172
CASE REPORT
Hepatitis-like onset of systemic lupus erythematosus in a 9-year-old female patient
Pediatr Pol 2025;100(2):177-182
CASE REPORT
A rare presentation of giant teratoma in the mediastinum of an adolescent – a case report and treatment outcome
Pediatr Pol 2025;100(2):183-188
CASE REPORT
Chronic kidney disease in a 7-year-old boy with an ultra-rare REN gene mutation. A case report and the literature review
Pediatr Pol 2025;100(2):189-194
CASE REPORT
A long way to a simple diagnosis – a case report of an overlooked juvenile polyp
Pediatr Pol 2025;100(2):195-198
CASE REPORT
Mutation of the NOP10 gene as a cause of steroid-resistant nephrotic syndrome coexisting with cataract, hearing loss, and enterocolitis
Pediatr Pol 2025;100(2):199-202
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