Document Detail

Familial functional antithrombin III deficiency.
MedLine Citation:
PMID:  7375809     Owner:  NLM     Status:  MEDLINE    
A family with a tendency to thrombosis and decreased antithrombin III (AT III) activity in plasma, but normal immunoreactive AT III is reported. 7 members of the family had the AT III defect, 4 of whom have had thrombotic episodes. The importance of biological determination of AT III when studying patients with recurrent thrombotic episodes is emphasized.
P J Sørensen; J Dyerberg; E Stoffersen; M K Jensen
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Scandinavian journal of haematology     Volume:  24     ISSN:  0036-553X     ISO Abbreviation:  Scand J Haematol     Publication Date:  1980 Feb 
Date Detail:
Created Date:  1980-07-28     Completed Date:  1980-07-28     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0404507     Medline TA:  Scand J Haematol     Country:  DENMARK    
Other Details:
Languages:  eng     Pagination:  105-9     Citation Subset:  IM    
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MeSH Terms
Antithrombin III / analysis,  genetics
Antithrombin III Deficiency*
Middle Aged
Pulmonary Embolism / blood,  complications,  genetics
Thrombophlebitis / blood,  complications,  genetics*
Reg. No./Substance:
81-81-2/Warfarin; 9000-94-6/Antithrombin III

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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