| Issue |
Section |
Title |
File |
| Vol 15, No 1 (2016) |
IMAGES |
Clinical case: Castleman’s disease |
(Rus)
|
| Vol 17, No 2 (2018) |
ШКОЛА ИММУНОЛОГА |
Clinical case of IgG4-related disease |
(Rus)
|
| 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 17, No 4 (2018) |
ШКОЛА ИММУНОЛОГА |
Treatment approaches to hyper-IgE syndrome: a clinical case report |
(Rus)
|
| Vol 18, No 2 (2019) |
ШКОЛА ИММУНОЛОГА |
Clinical case of proteasome-associated autoinflammatory syndrome-2 (PRAAS2) |
(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 3 (2020) |
ORIGINAL ARTICLES |
Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2 |
(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 |
(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 |
(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 |
Chronic nonbacterial osteomyelitis: single center experience |
(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 4 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
A case report of autoinflammation and PLCy2-associated antibody deficiency and immune dysregulation |
(Rus)
|
| Vol 22, No 2 (2023) |
ORIGINAL ARTICLES |
Experience with the use of Hizentra, an immunoglobulin preparation for subcutaneous administration, in patients with primary immunodeficiency diseases |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
An assessment of efficacy and safety of replacement therapy with subcutaneous immunoglobulin 16.5% administered by rapid push method in patients with inborn errors of immunity: the results of a prospective multicenter study |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Genetic diversity in pediatric patients with inborn errors of immunity in Russia |
(Rus)
|
| Vol 24, No 1 (2025) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Immune thrombocytopenia as the first symptom of primary immunodeficiency with immune dysregulation: a clinical case report and literature review |
(Rus)
|
