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Author

E. Raykina

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Open access Aug 2026

The molecular genetic spectrum of hereditary spherocytosis in the Russian population

Introduction. Hereditary spherocytosis (HS) is a hereditary hemolytic anemia caused by defects in erythrocyte membrane and cytoskeleton due to mutations mainly in five genes: ANK1, SPTB, SPTA1, SLC4A1, and EPB42. The genetic landscape of HS is characterized by considerable interpopulation variability. Aim – to investi...

M. Lunyakova, E. Raykina, S. G. Kapranova et al. · 0 citations
Open access Aug 2026

The role of allogeneic hematopoietic stem cell transplantation in the treatment of rare inherited bone marrow failure syndromes with cancer predisposition

Performing allo-HSCT before the development of advanced clonal evolution and malignant transformation is associated with improved long-term outcomes, suggesting a personalized approach based on the underlying genetic defect, clinical disease course, and evidence of clonal evolution allows for timely transplantation and...

M. S. Vasilyeva, A. Maschan, E. Raykina et al. · 0 citations

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