| Issue |
Section |
Title |
File |
| Vol 17, No 1 (2018) |
Статьи |
Diagnostics of inherited functional platelet disorders (IFPD) in children: correlations between results of flow cytometry, clinical phenotype and results of light transmission aggregometry |
(Rus)
|
| Vol 16, No 1 (2017) |
Статьи |
Modern approach to diagnosis of inherited functional platelet disorders |
(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 4 (2018) |
CLINICAL OBSERVATIONS |
The case of rare hereditary thrombocytopenia with a predisposition to the development of acute myeloid leukemia in twin children |
(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) |
LITERATURE REVIEW |
Platelet functional activity: physiology and laboratory diagnostic methods |
(Rus)
|
| Vol 19, No 1 (2020) |
ORIGINAL ARTICLES |
Observation of granulocyte function during ex vivo thrombus formation for patients with ANKRD26-associated thrombocytopenia |
(Rus)
|
| Vol 19, No 3 (2020) |
ORIGINAL ARTICLES |
The current status of remote diagnosis of von Willebrand disease in children in Russia |
(Rus)
|
| Vol 19, No 4 (2020) |
ORIGINAL ARTICLES |
Results of extended phenotyping of von Willebrand disease in the remote diagnostic program in children |
(Rus)
|
| Vol 20, No 1 (2021) |
ORIGINAL ARTICLES |
Specifities of the storage pool and morphology of platelets in children with unspecified hemorrhagic syndrome |
(Rus)
|
| Vol 20, No 1 (2021) |
CLINICAL OBSERVATIONS |
Pseudotumor of the maxilla as first presentation of hemophilia B in a 1-year-old male |
(Rus)
|
| Vol 20, No 2 (2021) |
ORIGINAL ARTICLES |
Platelet phenotype in children with ANKRD26-related thrombocytopenia |
(Rus)
|
| Vol 20, No 3 (2021) |
ORIGINAL ARTICLES |
Thrombopoietin receptor agonists for the treatment of severe persistent and chronic immune trombocytopenia in children: clinical data of Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology |
(Rus)
|
| Vol 20, No 3 (2021) |
ORIGINAL ARTICLES |
Thrombopoietin receptor agonists for the treatment of severe persistent and chronic immune trombocytopenia in children: clinical data of Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology |
(Rus)
|
| Vol 20, No 3 (2021) |
CLINICAL OBSERVATIONS |
Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI |
(Rus)
|
| Vol 21, No 1 (2022) |
CLINICAL OBSERVATIONS |
Congenital combined vitamin K-dependent clotting factors deficiency: case reports |
(Rus)
|
| Vol 21, No 2 (2022) |
ORIGINAL ARTICLES |
The THROMB-HEM study: first results and future prospects |
(Rus)
|
| Vol 21, No 2 (2022) |
CLINICAL OBSERVATIONS |
Immune tolerance induction with a high-purity von Willebrand factor containing plasma-derived factor VIII concentrate in a child with hemophilia A with inhibitors |
(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 22, No 3 (2023) |
ORIGINAL ARTICLES |
A single-center experience of using immunofluorescence staining of blood smears for the diagnosis of hereditary thrombocytopathies |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Thrombocytopenia of newborns: an observational study |
(Rus)
|
| Vol 23, No 4 (2024) |
ORIGINAL ARTICLES |
Diagnosis of type 2B von Willebrand disease in children |
(Rus)
|
