Issue |
Section |
Title |
File |
Vol 17, No 3 (2018) |
ORIGINAL ARTICLES |
Clinical experience using selective immunomodulating targeted therapy of Interstitial lymphocytic lung disease in a group of pediatric patients with primary immunodeficiencies |
 (Rus)
|
Vol 17, No 3 (2018) |
PROMISING STUDIES |
Therapy features of interstitial lymphocytic lung disease (ILLD) in patients with immune dysregulation syndromes: case report |
 (Rus)
|
Vol 18, No 3 (2019) |
CLINICAL OBSERVATIONS |
Clericusio syndrome (poikiloderm with neutropenia) |
 (Rus)
|
Vol 19, No 1 (2020) |
ШКОЛА ИММУНОЛОГА |
Rosay–Dorfman – like lymphadenopathy in a patient with Wiskott–Aldrich syndrome: diagnostic difficulties |
 (Rus)
|
Vol 19, No 3 (2020) |
ШКОЛА ИММУНОЛОГА |
A rare case of combined immunodeficiency due to a deletion of 11(q) – Jacobsen syndrome |
 (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 |
 (Rus)
|
Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Characteristics of a group of patients with WHIM syndrome |
 (Rus)
|
Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Chronic nonbacterial osteomyelitis: single center experience |
 (Rus)
|
Vol 20, No 1 (2021) |
ШКОЛА ИММУНОЛОГА |
Rare CVID-like phenotype of autoimmune lymphoproliferative syndrome |
 (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 3 (2021) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Clinical case of type I interferonopathy: homozygous STAT2 gain-of-function mutation |
 (Rus)
|
Vol 21, No 1 (2022) |
ORIGINAL ARTICLES |
Cryopyrin-associated periodic syndrome assess the efficacy and safety of anakinra therapy: a single center experience |
 (Rus)
|
Vol 21, No 3 (2022) |
ORIGINAL ARTICLES |
An autoinflammatory disease – PFAPA syndrome: a single-center experience |
 (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 1 (2023) |
CLINICAL OBSERVATIONS |
Secondary Fisher–Evans syndrome in a child with activated PI(3)kd syndrome and lymphoma |
 (Rus)
|
Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Genetic diversity in pediatric patients with inborn errors of immunity in Russia |
 (Rus)
|