| 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 18, No 3 (2019) |
ORIGINAL ARTICLES |
Fisher-Evans Syndrome in Children: an Analysis of Genetic Defects and Therapy Response |
 (Rus)
|
| Vol 18, No 3 (2019) |
CLINICAL OBSERVATIONS |
Clericusio syndrome (poikiloderm with neutropenia) |
 (Rus)
|
| Vol 20, No 2 (2021) |
ORIGINAL ARTICLES |
Evans syndrome in children: the results of a retrospective study of 54 patients |
 (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) |
CLINICAL OBSERVATIONS |
MECOM-associated syndrome: a literature review and case reports |
 (Rus)
|
| Vol 23, No 2 (2024) |
LITERATURE REVIEW |
Aplastic anemia in children: the current concept of differential diagnosis |
 (Rus)
|
| Vol 24, No 4 (2025) |
ORIGINAL ARTICLES |
The characterization of genetic defects in children with congenital neutropenia |
 (Rus)
|
| Vol 24, No 4 (2025) |
LITERATURE REVIEW |
Modern concepts of clonal hematopoiesis and its clinical significance in the development of hematologic malignancies |
 (Rus)
|
| Vol 25, No 1 (2026) |
ORIGINAL ARTICLES |
Somatic oncogenic events in Shwachman–Diamond syndrome: molecular genetic characterization and clinical significance |
 (Rus)
|