| Issue |
Section |
Title |
File |
| Vol 16, No 4 (2017) |
Статьи |
Genetic and clinical characteristics of a group of patients with hereditary angioedema type 1 and 2 |
(Rus)
|
| Vol 17, No 1 (2018) |
Статьи |
Sirolimus efficacy in treatment of autoimmune lymphoproliferative syndrome |
(Rus)
|
| Vol 17, No 1 (2018) |
Статьи |
Description of the familial case of Wiskott–Aldrich syndrome with mild phenotype |
(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 18, No 4 (2019) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Granulomatous inflammation in the manifestation of chronic granulomatous disease: a clinical case report |
(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 |
TREC/KREC analysis for the postnatal diagnosis of primary immunodeficiency diseases |
(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 20, No 4 (2021) |
ORIGINAL ARTICLES |
Analysis of familial cases of primary immunodeficiency in the context of genetic counseling |
(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 1 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
A case of medulloblastoma in a patient with hereditary angioedema with C1 inhibitor deficiency |
(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 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)
|
