Author Details

Khoreva, A. L.

Issue Section Title File
Vol 18, No 2 (2019) CLINICAL OBSERVATIONS The phenomenon of conversion of the donor-derived blood group to the patient’s original blood group after ABO-incompatible hematopoietic stem cell transplantation in a patient with Wiskott–Aldrich syndrome PDF
(Rus)
Vol 19, No 1 (2020) CLINICAL SIGNIFICANCE OF BASIC RESEARCH Specific features of intracellular calcium signalling, distinctive for Wiskott-Aldrich syndrome patients PDF
(Rus)
Vol 19, No 1 (2020) ШКОЛА ИММУНОЛОГА Rosay–Dorfman – like lymphadenopathy in a patient with Wiskott–Aldrich syndrome: diagnostic difficulties PDF
(Rus)
Vol 19, No 2 (2020) ORIGINAL ARTICLES Development of flow cytometry assay for Wiskott–Aldrich syndrome diagnosis by WASP protein evaluation PDF
(Rus)
Vol 19, No 4 (2020): supplement MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS The efficacy and safety of romiplostim in the treatment of thrombocytopenia in pediatric patients with Wiskott–Aldrich syndrome: the results of a retrospective study PDF
(Rus)
Vol 19, No 4 (2020): supplement MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS Non-infectious complications in the group of pediatric patients with chronic granulomatous disease PDF
(Rus)
Vol 19, No 4 (2020): supplement MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS Chromosomal aberrations as the cause of a complex phenotype in children with primary immunodeficiencies PDF
(Rus)
Vol 20, No 2 (2021) SCHOOL OF IMMUNOLOGY – EXPERT OPINION Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation PDF
(Rus)
Vol 20, No 2 (2021) SCHOOL OF IMMUNOLOGY – EXPERT OPINION Long-term persistent mixed chimerism in a patient with Wiskott–Aldrich syndrome after allogeneic hematopoietic stem cell transplantation PDF
(Rus)
Vol 21, No 4 (2022) SCHOOL OF IMMUNOLOGY – EXPERT OPINION A case report of autoinflammation and PLCy2-associated antibody deficiency and immune dysregulation PDF
(Rus)
Vol 21, No 4 (2022) CLINICAL OBSERVATIONS Newborn screening for primary immunodeficiencies as a way to detect syndromal disorders in neonates: a clinical case of 22q11.2DS syndrome PDF
(Rus)
Vol 22, No 3 (2023) ORIGINAL ARTICLES A single-center experience of using immunofluorescence staining of blood smears for the diagnosis of hereditary thrombocytopathies PDF
(Rus)