Found: 11
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Glycoprotein Ibα Promoter Drives Megakaryocytic Lineage-Restricted Expression After Hematopoietic Stem Cell Transduction Using a Self-Inactivating Lentiviral Vector.
- Published in:
- Stem Cells, 2007, v. 25, n. 6, p. 1571, doi. 10.1634/stemcells.2006-0321
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- Article
High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard–Soulier syndrome in French patients from the genetic isolate of Reunion Island.
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- British Journal of Haematology, 2020, v. 189, n. 3, p. e67, doi. 10.1111/bjh.16479
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- Article
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders.
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- British Journal of Haematology, 2015, v. 170, n. 4, p. 559, doi. 10.1111/bjh.13458
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- Article
Apoptotic Platelet Events Are Not Observed in Severe von Willebrand Disease-Type 2B Mutation p.V1316M.
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- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0143896
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- Article
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.
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- Human Genetics, 2010, v. 127, n. 1, p. 45, doi. 10.1007/s00439-009-0742-6
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- Article
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.
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- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02787-2
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- Article
Pulmonary Artery Thrombosis during Acute Chest Syndrome in Sickle Cell Disease.
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- American Journal of Respiratory & Critical Care Medicine, 2011, v. 184, n. 9, p. 1022, doi. 10.1164/rccm.201105-0783OC
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- Article
Déficit en granules denses plaquettaires : une cause sous-estimée de saignements inexpliqués: Document élaboré sous l'égide du Centrede référence des pathologies plaquettaires constitutionnelles.
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- Hematologie, 2017, v. 23, n. 4, p. 243, doi. 10.1684/hma.2017.1287
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- Article
Interferences by factor VIII and lupus anticoagulant in the modified one‐stage assay for emicizumab.
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- Haemophilia, 2023, v. 29, n. 6, p. 1661, doi. 10.1111/hae.14873
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- Article
FVIII dosages in persons with haemophilia A treated with extended half‐life products: From local biology to optimized patient management.
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- Haemophilia, 2019, v. 25, n. 6, p. e361, doi. 10.1111/hae.13801
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- Article
Management of congenital quantitative fibrinogen disorders: a Delphi consensus.
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- Haemophilia, 2016, v. 22, n. 6, p. 898, doi. 10.1111/hae.13061
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- Article