| Issue |
Section |
Title |
File |
| Vol 16, No 4 (2017) |
Статьи |
Clinical and laboratory characteristics of a group of patients with autoimmune lymphoproliferative syndrome |
(Rus)
|
| Vol 17, No 1 (2018) |
Статьи |
Sirolimus efficacy in treatment of autoimmune lymphoproliferative syndrome |
(Rus)
|
| Vol 14, No 3 (2015) |
CLINICAL PHARMACOLOGY AND PHARMACOTHERAPY |
Intravenous 5% normal human immunoglobulin I.G. Vena in therapy of primary immunodeficiencies in children |
(Rus)
|
| Vol 15, No 1 (2016) |
IMAGES |
BCG-related macrophage activation syndrom e in patients with severe combined immunodeficiency after hematopoietic stem cell transplantation |
(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 3 (2020) |
ORIGINAL ARTICLES |
Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2 |
(Rus)
|
| Vol 19, No 4 (2020) |
ORIGINAL ARTICLES |
Verification of X-linked lymphoproliferative syndrome type 1 and 2 using a flow cytometry method |
(Rus)
|
| Vol 19, No 4 (2020) |
CLINICAL OBSERVATIONS |
Epstein–Barr virus-associated smooth muscle tumors in patients with primary immunodeficiencies |
(Rus)
|
| Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Immunoglobulin replacement therapy in patients with primary immunodeficiency diseases in Russia |
(Rus)
|
| Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Influence of clinical and immunophenotypic variants of severe combined immunodeficiency on severity and outcomes of opportunistic infections |
(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 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 |
(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 |
(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 2 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
A familial case of Louis–Bar syndrome |
(Rus)
|
| Vol 21, No 3 (2022) |
ORIGINAL ARTICLES |
Clinical and laboratory characteristics of a group of patients with ataxia-telangiectasia syndrome |
(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 |
X-linked agammaglobulinemia: a review of literature and a case report |
(Rus)
|
| Vol 22, No 1 (2023) |
ORIGINAL ARTICLES |
The assessment of the efficacy and safety of the personalized rehabilitation of the second stage using modern methods and technologies in children with primary immunodeficiencies |
(Rus)
|
| Vol 22, No 1 (2023) |
ORIGINAL ARTICLES |
Treatment of lymphoid malignancies in patients with primary immunodeficiencies associated with DNA repair defects |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Thrombocytopenia of newborns: an observational study |
(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)
|
