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Anna Pavlova

dmitry rogachev national medical research center of pediatric hematology, oncology and immunology
H-index:27
Citation Count:3,359
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Altered cytoskeletal integrity underlies impaired platelet shape change and defective thrombus formation in ETV6-related thrombocytopenia

ETV6相关血小板减少症中细胞骨架完整性的改变导致血小板形态变化受损和血栓形成缺陷

2026-04-280
OAAI
Weighted Ensemble Simulations Reveal Novel Conformations and Modulator Effects in Hepatitis B Virus Capsid Assembly

加权群集模拟揭示了乙型肝炎病毒衣壳组装的新型构象和调节剂效应

2025-11-010
PRE
INHERITED BONE MARROW FAILURE WITH A PREDISPOSITION TO MYELODYSPLASTIC SYNDROMES/ ACUTE MYELOID LEUKEMIA IN CHILDREN
2025-11-010
OAAI
Understanding Congenital FXI Deficiency: Genetic Diagnosis and Correlation of Variant Detection Rate to Factor XI Activity

理解先天性FXI缺乏症:基因诊断及变异检出率与因子XI活性的相关性

2025-10-010
PRE
The Diagnostic Assessment of Inherited Platelet Function Defects

遗传性血小板功能缺陷的诊断评估

2025-01-270
PRE
The Diagnostic Assessment of Platelet Function Defects

血小板功能缺陷的诊断评估

2025-01-271
PRE
Modulation of Haemostatic Balance in Combined von Willebrand Disease and Antithrombin Deficiency: A Comprehensive Family Study
2024-12-190
OA
Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiency
2024-02-012
PRE
Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations
2022-07-076
OAAI
Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study

Simococog Alfa (Nuwiq) 在先前未经治疗的严重血友病A患者中: NuProtect研究的最终结果

2021-02-1320
OAAI
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic Diagnosis
2021-01-1813
OAAI
Supercomputer-Based Ensemble Docking Drug Discovery Pipeline with Application to Covid-19
2020-12-16130
OAAI
The Clinical and Genetic Spectrum of 82 Patients WithRAGDeficiency Including a c.256_257delAA Founder Variant in Slavic Countries
2020-06-1015
OAAI
Recommendations for clinical laboratory testing for protein C deficiency, for the subcommittee on plasma coagulation inhibitors of the ISTH

对于ISTH血浆凝血抑制剂小组委员会的蛋白C缺乏症临床实验室测试的建议

2020-02-0134
PRE
Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease
2019-09-187
OAAI
The role of variant alleles of the mannose-binding lectin in the inhibitor development in severe hemophilia A
2019-07-013
PREAI
Beyond the bleeding rates- HEAD-US joint assessment in patients treated by late prophylaxis
2019-05-276
PREAI
In silico and in vitro evaluation of the impact of mutations in non-severe haemophilia A patients on assay discrepancies
2019-04-179
PREAI
Role of factor VIII-binding capacity of endogenous von Willebrand factor in the development of factor VIII inhibitors in patients with severe hemophilia A
2019-01-313
OA