| Issue |
Section |
Title |
File |
| Vol 17, No 1 (2018) |
Статьи |
Description of the familial case of Wiskott–Aldrich syndrome with mild phenotype |
(Rus)
|
| Vol 16, No 1 (2017) |
Статьи |
Herpesvirus infection following allogenic hematopoietic stem cell transplantation with TCRαβ and CD19 depletion: risk factors and outcome |
(Rus)
|
| Vol 17, No 2 (2018) |
ORIGINAL ARTICLES |
The Influence of Natural Killer Cell Alloreactivity on the Outcome of α/βTCR/CD19+ depleted Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Patients with Acute Leukemia |
(Rus)
|
| Vol 17, No 4 (2018) |
CLINICAL OBSERVATIONS |
The case of rare hereditary thrombocytopenia with a predisposition to the development of acute myeloid leukemia in twin children |
(Rus)
|
| Vol 18, No 3 (2019) |
CLINICAL OBSERVATIONS |
ANKRD26-related thrombocytopenia: case report and literature review of inherited thrombocytopenias with predisposition to malignancies |
(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 3 (2020) |
ORIGINAL ARTICLES |
Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2 |
(Rus)
|
| Vol 19, No 3 (2020) |
CLINICAL OBSERVATIONS |
Diagnostic challenges in pyruvate kinase deficiency |
(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 |
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 |
Characteristics of a group of patients with WHIM syndrome |
(Rus)
|
| Vol 20, No 2 (2021) |
ORIGINAL ARTICLES |
Platelet phenotype in children with ANKRD26-related thrombocytopenia |
(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) |
CLINICAL OBSERVATIONS |
Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI |
(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 3 (2022) |
SCHOOL OF IMMUNOLOGY – EXPERT OPINION |
Clinical characteristics of patients with the SAMD9/SAMD9L gene defects |
(Rus)
|
| Vol 21, No 3 (2022) |
ORIGINAL ARTICLES |
Clinical and laboratory characteristics of a group of patients with ataxia-telangiectasia syndrome |
(Rus)
|
| Vol 22, No 1 (2023) |
CLINICAL OBSERVATIONS |
Resistance to BRAF inhibitors in a patient with BRAF V600E-positive Langerhans cell histiocytosis |
(Rus)
|
| Vol 22, No 1 (2023) |
PROMISING STUDIES |
The use of droplet digital polymerase chain reaction for the molecular diagnosis and monitoring of treatment response in patients with Langerhans cell histiocytosis with the BRAF V600E mutation |
(Rus)
|
| Vol 22, No 1 (2023) |
ORIGINAL ARTICLES |
Treatment of lymphoid malignancies in patients with primary immunodeficiencies associated with DNA repair defects |
(Rus)
|
| Vol 22, No 3 (2023) |
CLINICAL OBSERVATIONS |
Age-dependent changes in platelet function of a patient with SLFN14-related macrothrombocytopenia |
(Rus)
|
| Vol 22, No 4 (2023) |
ORIGINAL ARTICLES |
Clinicogenomic associations in patients with Langerhans cell histiocytosis: a cohort study |
(Rus)
|
| Vol 23, No 1 (2024) |
ORIGINAL ARTICLES |
The results of a study on the effectiveness 37 and safety of treatment with vemurafenib and cytarabine/2-chloro-2′-deoxyadenosine combination in patients with Langerhans cell histiocytosis with BRAFV600E mutation |
(Rus)
|
| Vol 23, No 2 (2024) |
LITERATURE REVIEW |
Aplastic anemia in children: the current concept of differential diagnosis |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Thrombocytopenia of newborns: an observational study |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Genetic diversity in pediatric patients with inborn errors of immunity in Russia |
(Rus)
|
| Vol 23, No 4 (2024) |
CLINICAL OBSERVATIONS |
Iron-refractory iron deficiency anemia in children: first genetically confirmed cases in Russia |
(Rus)
|
