Found: 6
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Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations.
- Published in:
- British Journal of Haematology, 2019, v. 186, n. 4, p. e100, doi. 10.1111/bjh.15931
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- Publication type:
- Article
New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.
- Published in:
- British Journal of Haematology, 2019, v. 184, n. 5, p. 855, doi. 10.1111/bjh.15176
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- Publication type:
- Article
Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA‐DRB1*11 and DQB1*03 antigens.
- Published in:
- 2018
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- Publication type:
- Case Study
Activated Platelet‐Derived and Leukocyte‐Derived Circulating Microparticles and the Risk of Thrombosis in Heparin‐Induced Thrombocytopenia: A Role for PF4‐Bearing Microparticles?
- Published in:
- Cytometry. Part B, 2018, v. 94, n. 2, p. 334, doi. 10.1002/cyto.b.21507
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- Publication type:
- Article
Presence of anti-ADAMTS13 antibodies in obesity.
- Published in:
- European Journal of Clinical Investigation, 2012, v. 42, n. 11, p. 1197, doi. 10.1111/j.1365-2362.2012.02710.x
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- Publication type:
- Article
A performance-based framework for adaptive seismic aftershock risk assessment.
- Published in:
- Earthquake Engineering & Structural Dynamics, 2014, v. 43, n. 14, p. 2179, doi. 10.1002/eqe.2444
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- Publication type:
- Article