Ataksja Friedreicha — aktualne spojrzenie na chorobę

Zuzanna Niwińska

Vol 33, No 61 (2023): Continuous Publishing

Review paper

Phelan-McDermid syndrome and seizures provoked by fever — clinical and electroencephalographic comparisons of two patients

Anna Winczewska-Wiktor, Paulina Komasińska-Piotrowska, Ewa Gajewska, Barbara Steinborn

Vol 33, No 61 (2023): Continuous Publishing

Review paper

Vitamin B12 deficiency encephalopaty as a potentially reversible brain injury — case study based on several years of a patient’s observation

Anna Frączek-Szczepkowska

Vol 33, No 61 (2023): Continuous Publishing

Case report

Unraveling the complexities of CDKL5 deficiency disorder: Is an emerging treatment on the horizon?

Klaudia Bartoszewicz, Barbara Steinborn

Vol 33, No 61 (2023): Continuous Publishing

Review paper

Ensuring continuity and development of spinal muscular atrophy treatment in Poland

Katarzyna Kotulska-Jóźwiak, Monika Gos, Anna Kostera-Pruszczyk, Justyna Paprocka, Agnieszka Słowik, Marcin Czech, Jakub Gierczyński, Maria Mazurkiewicz-Bełdzińska

Vol 34, No 62 (2024): Continuous Publishing

Editorial

miRNAs as potential biomarkers for childhood epilepsy

Beata Rzepka-Migut, Justyna Paprocka

Vol 33, No 61 (2023): Continuous Publishing

Review paper

Limbic encephalitis in children

Maciej Kamiński, Justyna Paprocka

Vol 33, No 61 (2023): Continuous Publishing

Review paper

IX Zjazd Polskiego Towarzystwa Neurologów Dziecięcych

Krystyna Mitosek-Szewczyk

Vol 33, No 61 (2023): Continuous Publishing

Editorial

Treatment of drooling in children and adolescents with neurological disorders

Malwina Bocianiak, Barbara Steinborn

Vol 33, No 61 (2023): Continuous Publishing

Review paper

Research on the treatment of Rett syndrome

Oliwia Gorgoń-Dezor

Vol 33, No 61 (2023): Continuous Publishing

Case report

Damage to the nerve roots of the brachial plexus in the course of Lyme disease in a 15-year-old girl

Wiktoria Sielwanowska, Natalia Wilczek, Estera Penar, Karolina Witaszek, Magdalena Ociepa, Michał Pytlak, Magdalena Chrościńska-Krawczyk

Vol 34, No 62 (2024): Continuous Publishing

Case report

Progressive epileptic encephalopathy due to mutations in the HSD17B gene — bifunctional enzyme deficiency. A case report

Sylwia Maria Pawlak-Kurek, Łukasz Przysło

Vol 34, No 62 (2024): Continuous Publishing

Case report