Aleksandra Kozińska

Frequency and predictors of blood transfusion and splenectomy in pediatric hereditary spherocytosis – a single-center retrospective analysis

Aleksandra Osińska, Marta Druszcz, Maksymilian Seweryn, Natalia Czarnecka et autres

Introduction Hereditary spherocytosis (HS) is the most common hereditary hemolytic anemia among children in Europe. It is characterized by membrane protein defects leading to spherocyte formation and increased hemolysis. Hereditary spherocytosis can present with a wide spectrum of clinical severity, from asymptomatic …

pl (code pays fourni par la source)

Exploring treatment approaches for Neuromyelitis Optica Spectrum Disorders (NMOSD)

Aleksandra Kozińska, Anna Jamróz-Wiśniewska, Konrad Rejdak

Introduction and Objective.Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune demyelinating disease of the central nervous system, distinct from multiple sclerosis.Its pathogenesis is primarily associated with anti-AQP4-IgG antibodies, though some patients present with anti-MOG-IgG.The most common symptoms include optic neuritis and …

pl, us (code pays fourni par la source)

120P Pigmentation level of uveal melanoma and its development

Justyna Sopel, Aleksandra Kozińska, M. Szczygieł, A. Markiewicz et autres