Works matching IS 00015792 AND DT 2023 AND VI 146 AND IP 3
Results: 12
Acquired Von Willebrand Syndrome following a SARS-CoV2 Infection.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 226, doi. 10.1159/000529740
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- Article
Front & Back Matter.
- Published in:
- Acta Haematologica, 2023, v. 146, n. 3, p. 1, doi. 10.1159/000531365
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- Article
Therapeutic Efficacy of Platelet Transfusion and Analysis of Influencing Factors in 364 patients.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 214, doi. 10.1159/000529542
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A Longitudinal Assessment of the Natural Change in Haemoglobin, Haematocrit, and Mean Corpuscular Volume with Age.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 206, doi. 10.1159/000529356
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- Article
Macrocytosis in Mitochondrial DNA Deletion Syndromes.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 220, doi. 10.1159/000529311
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- Article
High Expression of CD300A Predicts Poor Survival in Acute Myeloid Leukemia.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 196, doi. 10.1159/000529078
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- Article
Disparity Analysis of Clinical Features and Prognostic Evaluation of Hemophagocytic Lymphohistiocytosis in Pediatric and Adult Patients: A Retrospective Multicenter Study of 525 Cases in HHLWG.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 185, doi. 10.1159/000528934
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- Article
Efficacy and Incidence of Treatment-Related Adverse Events of Thrombopoietin Receptor Agonists in Adults with Immune Thrombocytopenia: A Systematic Review and Network Meta-Analysis of Randomized Controlled Study.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 173, doi. 10.1159/000528642
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- Article
Erdheim-Chester Disease with BRAF V600E Mutation and a Concomitant Myeloid Malignancy Sharing NRAS and IDH2 Mutations.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 245, doi. 10.1159/000528550
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- Article
On Behalf of the SFGM-TC: Prophylactic Donor Lymphocyte Infusion in Patients Treated with Allogeneic Stem-Cell Transplantation for High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 230, doi. 10.1159/000528184
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- Article
Glomerulonephritis Secondary to Acute Promyelocytic Leukemia that Resolved after Induction Therapy.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 240, doi. 10.1159/000528088
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- Article
Two Novel Heterozygous Mutations (p.γPhe230Val and p.AαAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families.
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- Acta Haematologica, 2023, v. 146, n. 3, p. 252, doi. 10.1159/000527952
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- Article