Issue |
Section |
Title |
File |
Vol 17, No 1 (2018) |
Статьи |
Bone marrow cell morphology in congenital diserythropoietic anemia: selective enrichment of the studied cell population for light and electron microscopy using a microarray and centrifugation in a density gradient |
 (Rus)
|
Vol 16, No 3 (2017) |
Статьи |
MRI T2*-mapping for liver iron assessment in pediatric patients with secondary iron overload |
 (Rus)
|
Vol 16, No 3 (2017) |
Статьи |
Inherited disorders of iron metabolism |
 (Rus)
|
Vol 14, No 3 (2015) |
CLINICAL OBSERVATIONS |
A clinical case report of acute intermittent porphyria in a patient aged 9 years |
 (Rus)
|
Vol 17, No 2 (2018) |
LITERATURE REVIEW |
Economic methods of medical technology assessment in hematology |
 (Rus)
|
Vol 18, No 3 (2019) |
ORIGINAL ARTICLES |
Epilemiological characteristics of Diamond–Blackfen anemia in pediatric population of the Russian Federation |
 (Rus)
|
Vol 18, No 3 (2019) |
ORIGINAL ARTICLES |
Fisher-Evans Syndrome in Children: an Analysis of Genetic Defects and Therapy Response |
 (Rus)
|
Vol 19, No 3 (2020) |
LITERATURE REVIEW |
Pyruvat kinase deficiency and nonspherocytic hemolytic anemia |
 (Rus)
|
Vol 19, No 4 (2020): supplement |
MATERIALS OF THE 3rd WORKING MEETING OF ALLERGISTS-IMMUNOLOGISTS |
Fisher–Evans syndrome in children: an analysis of data from the D. Rogachev NMRCPHOI |
 (Rus)
|
Vol 20, No 1 (2021) |
ШКОЛА ИММУНОЛОГА |
Rare CVID-like phenotype of autoimmune lymphoproliferative syndrome |
 (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 20, No 3 (2021) |
ORIGINAL ARTICLES |
Endothelial dysfunction in patients with hereditary spherocytosis and b-thalassemia |
 (Rus)
|
Vol 21, No 3 (2022) |
ORIGINAL ARTICLES |
Unstable abnormal hemoglobins found in Russia in the past 10 years |
 (Rus)
|
Vol 23, No 2 (2024) |
ORIGINAL ARTICLES |
Red blood cell filterability measurement in the diagnosis of hereditary spherocytosis |
 (Rus)
|
Vol 24, No 1 (2025) |
ORIGINAL ARTICLES |
Von Willebrand factor multimer profile and function in children and young adults with essential thrombocythemia |
 (Rus)
|
Vol 24, No 1 (2025) |
ORIGINAL ARTICLES |
Selective enrichment of rare bone marrow cell populations for electron microscopy |
 (Rus)
|