Hereditary α2-antiplasmin deficiency
- 15 August 1983
- journal article
- research article
- Published by Elsevier in Thrombosis Research
- Vol. 31 (4) , 647-651
- https://doi.org/10.1016/0049-3848(83)90462-0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- A familial hemorrhagic diathesis in a Dutch family: an inherited deficiency of alpha 2-antiplasminBlood, 1982
- Diagnosis of Heterozygotes in Glanzmann’s ThrombastheniaThrombosis and Haemostasis, 1982
- Fibrinolytic states in a patient with congenital deficiency of alpha 2- plasmin inhibitorBlood, 1980
- The Thrombo‐Haemorrhagic BalanceActa Medica Scandinavica, 1980
- HOMOZYGOUS $alpha;2-ANTIPLASMIN DEFICIENCYThe Lancet, 1979
- Congenital Deficiency of α2-Plasmin Inhibitor Associated with Severe Hemorrhagic Tendency *Journal of Clinical Investigation, 1979
- α2-PLASMIN-INHIBITOR DEFICIENCY (MIYASATO DISEASE)The Lancet, 1978
- Increased Blood Fibrinolytic Activity after Aspirin IngestionNew England Journal of Medicine, 1977
- Demonstration of Low Content of Fibrinolytic Inhibitors in Individuals with High Fibrinolytic CapacityScandinavian Journal of Clinical and Laboratory Investigation, 1970
- Proteolytic Capacity in Human Plasma Part II Genetics, and clinical studyScandinavian Journal of Clinical and Laboratory Investigation, 1968