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 16, No 4 (2017) |
Статьи |
Genetic and clinical characteristics of a group of patients with hereditary angioedema type 1 and 2 |
 (Rus)
|
Vol 16, No 1 (2017) |
Статьи |
MYH9-related inherited thrombocytopenia |
 (Rus)
|
Vol 14, No 4 (2015) |
CLINICAL OBSERVATIONS |
Clinical manifestations and laboratory features of acute parvovirus infection in children with oncohematological diseases (Review of literature and clinical case reports) |
 (Rus)
|
Vol 18, No 2 (2019) |
ШКОЛА ИММУНОЛОГА |
Clinical case of proteasome-associated autoinflammatory syndrome-2 (PRAAS2) |
 (Rus)
|
Vol 19, No 3 (2020) |
ORIGINAL ARTICLES |
The spectrum of genetic variants of the a- and b-globin clusters in patients with hemoglobinopathies living in the Republic of Dagestan |
 (Rus)
|
Vol 19, No 4 (2020) |
ORIGINAL ARTICLES |
Low-grade gliomas with the V600E mutation in the BRAF gene in children: clinical features and treatment options |
 (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 2 (2021) |
ORIGINAL ARTICLES |
Non-spherocytic hemolytic anemia caused by erythrocyte pyruvate kinase defiiency: the analysis of genetic defects in pediatric patients, living in Russian Federation |
 (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)
|