A combined approach using global coagulation assays quickly differentiates coagulation disorders with prolonged aPTT and low levels of FVIII activity
Author:
Funder
KAKENHI MEXT
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-016-2108-x.pdf
Reference22 articles.
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2. Kessler CM, Knöbl P. Acquired haemophilia: an overview for clinical practice. Eur J Haematol. 2015;95(Suppl 81):36–44.
3. Robertson B, Greaves M. Antiphospholipid syndrome: an evolving story. Blood Rev. 2006;20:201–12.
4. Baca V, Montiel G, Meillón L, Pizzuto J, Catalan T, Juan-Shum L, et al. Diagnosis of lupus anticoagulant in the lupus anticoagulant hypoprothrombinemia syndrome: report of two cases and review of the literature. Am J Hematol. 2002;71:200–7.
5. Oldenburg J, Pavlova A. Discrepancy between one-stage and chromogenic factor VIII activity assay results can lead to misdiagnosis of haemophilia A phenotype. Hamostaseologie. 2010;30:207–11.
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