Disease | thromboembolism |
Phenotype | C0272375|antithrombin deficiency |
Sentences | 3 |
PubMedID- 23807486 | Antithrombin rybnik: a new point mutation (nt 683 g>t) associated with type i antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosis. |
PubMedID- 24686101 | Perioperative and peripartum prevention of venous thromboembolism in patients with hereditary antithrombin deficiency using recombinant antithrombin therapy. |
PubMedID- 23662090 | Prevention and treatment of venous thromboembolism in pregnancy in patients with hereditary antithrombin deficiency. |
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