Issue |
Section |
Title |
File |
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 |
ANKRD26-related thrombocytopenia: case report and literature review of inherited thrombocytopenias with predisposition to malignancies |
 (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 4 (2021) |
ORIGINAL ARTICLES |
Pediatric cystic nephroma: clinical and molecular genetic characteristics |
 (Rus)
|
Vol 20, No 3 (2021) |
CLINICAL OBSERVATIONS |
Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI |
 (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 4 (2022) |
CLINICAL OBSERVATIONS |
A familial case of DICER1 syndrome in a patient with pleuropulmonary blastoma |
 (Rus)
|
Vol 21, No 3 (2022) |
CLINICAL OBSERVATIONS |
MECOM-associated syndrome: a literature review and case reports |
 (Rus)
|
Vol 22, No 1 (2023) |
CLINICAL OBSERVATIONS |
Secondary Fisher–Evans syndrome in a child with activated PI(3)kd syndrome and lymphoma |
 (Rus)
|
Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Thrombocytopenia of newborns: an observational study |
 (Rus)
|