Issue |
Section |
Title |
File |
Vol 17, No 1 (2018) |
Статьи |
Description of the familial case of Wiskott–Aldrich syndrome with mild phenotype |
 (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) |
CLINICAL OBSERVATIONS |
Family case hemolytic anemia due to abnormal unstable hemoglobin with low oxygen affinity (Hb Cheverly) |
 (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 3 (2020) |
ORIGINAL ARTICLES |
Haematological complications of X-linked lymphoproliferative syndrome type 1 and 2 |
 (Rus)
|
Vol 19, No 3 (2020) |
CLINICAL OBSERVATIONS |
Transfusion-dependent phenotype of thalassemia in case of combined carriage of globin genes abnormalities: a-globin gene triplikation and b-thalassemia |
 (Rus)
|
Vol 19, No 4 (2020) |
CLINICAL OBSERVATIONS |
Epstein–Barr virus-associated smooth muscle tumors in patients with primary immunodeficiencies |
 (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) |
CLINICAL OBSERVATIONS |
First cases of Hb Lepore in the Russian Federation |
 (Rus)
|
Vol 20, No 3 (2021) |
CLINICAL OBSERVATIONS |
Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI |
 (Rus)
|
Vol 21, No 3 (2022) |
ORIGINAL ARTICLES |
Unstable abnormal hemoglobins found in Russia in the past 10 years |
 (Rus)
|
Vol 21, No 3 (2022) |
CLINICAL OBSERVATIONS |
Rare unstable hemoglobin Hakkari in Russia: a case report and literature review |
 (Rus)
|