Issue |
Section |
Title |
File |
Vol 18, No 3 (2019) |
ORIGINAL ARTICLES |
Fisher-Evans Syndrome in Children: an Analysis of Genetic Defects and Therapy Response |
 (Rus)
|
Vol 18, No 3 (2019) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
The phenomenon of reverse mutation in a patient with Wiskott–Aldrich syndrome |
 (Rus)
|
Vol 19, No 2 (2020) |
ORIGINAL ARTICLES |
Development of flow cytometry assay for Wiskott–Aldrich syndrome diagnosis by WASP protein evaluation |
 (Rus)
|
Vol 19, No 4 (2020) |
CLINICAL OBSERVATIONS |
Epstein–Barr virus-associated smooth muscle tumors in patients with primary immunodeficiencies |
 (Rus)
|
Vol 20, No 2 (2021) |
ORIGINAL ARTICLES |
Evans syndrome in children: the results of a retrospective study of 54 patients |
 (Rus)
|
Vol 20, No 2 (2021) |
ORIGINAL ARTICLES |
Platelet phenotype in children with ANKRD26-related thrombocytopenia |
 (Rus)
|
Vol 21, No 3 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Clinical characteristics of patients with the SAMD9/SAMD9L gene defects |
 (Rus)
|
Vol 21, No 4 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
A case report of autoinflammation and PLCy2-associated antibody deficiency and immune dysregulation |
 (Rus)
|
Vol 22, No 3 (2023) |
CLINICAL OBSERVATIONS |
Age-dependent changes in platelet function of a patient with SLFN14-related macrothrombocytopenia |
 (Rus)
|
Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Genetic diversity in pediatric patients with inborn errors of immunity in Russia |
 (Rus)
|