109 related articles for article (PubMed ID: 6724355)
1. Hereditary antithrombin III deficiency: biochemical aspects.
Sas G
Haematologia (Budap); 1984; 17(1):81-6. PubMed ID: 6724355
[TBL] [Abstract][Full Text] [Related]
2. Heterogeneity of the "classical" antithrombin III deficiency.
Sas G; Petö I; Bánhegyi D; Blaskó G; Domján G
Thromb Haemost; 1980 Jun; 43(2):133-6. PubMed ID: 7455972
[TBL] [Abstract][Full Text] [Related]
3. Antithrombin III deficiency.
Cucuianu M; Blaga S; Pop S; Olinic D; Olinic N; Colhon D; Cristea A
Rom J Intern Med; 1994; 32(2):119-27. PubMed ID: 7920326
[TBL] [Abstract][Full Text] [Related]
4. AT III Barcelona: a familial quantitative-qualitative AT III deficiency.
Grau E; Fontcuberta J; Félez J; de Diego I; Soto R; Rutllant ML
Thromb Haemost; 1988 Feb; 59(1):13-7. PubMed ID: 3363529
[TBL] [Abstract][Full Text] [Related]
5. Antithrombin III "Northwick Park": a variant antithrombin with normal affinity for heparin but reduced heparin cofactor activity.
Howarth DJ; Samson D; Stirling Y; Seghatchian MJ
Thromb Haemost; 1985 Jun; 53(3):314-9. PubMed ID: 4049307
[TBL] [Abstract][Full Text] [Related]
6. Homozygous or compound heterozygous qualitative antithrombin III deficiency.
Cucuianu M; Blaga S; Pop S; Olinic D; Olinic N; Colhon D; Cristea A
Nouv Rev Fr Hematol (1978); 1994 Aug; 36(4):335-7. PubMed ID: 7971256
[TBL] [Abstract][Full Text] [Related]
7. Purification and characterization of hereditary abnormal antithrombin III with impaired thrombin binding.
Jørgensen M; Petersen LC; Thorsen S
J Lab Clin Med; 1984 Aug; 104(2):245-56. PubMed ID: 6747440
[TBL] [Abstract][Full Text] [Related]
8. [A case of familial antithrombin III variant complicated by recurrent pulmonary infarction].
Nakano Y; Sato A; Okano A; Chida K; Yasumi T
Nihon Kyobu Shikkan Gakkai Zasshi; 1993 Feb; 31(2):214-8. PubMed ID: 8515601
[TBL] [Abstract][Full Text] [Related]
9. A tentative classification of AT III congenital abnormalities.
Girolami A
Folia Haematol Int Mag Klin Morphol Blutforsch; 1987; 114(5):661-9. PubMed ID: 2448207
[TBL] [Abstract][Full Text] [Related]
10. Inherited antithrombin III deficiency and cerebral thrombosis in a child.
Ambruso DR; Jacobson LJ; Hathaway WE
Pediatrics; 1980 Jan; 65(1):125-31. PubMed ID: 7355006
[TBL] [Abstract][Full Text] [Related]
11. Antithrombin III Padua: a "new" congenital antithrombin III abnormality with normal or near normal activity, normal antigen, abnormal migration and no thrombotic disease.
Girolami A; Pengo V; Cappellato G; Vianello C; Procidano M; Cartei C
Folia Haematol Int Mag Klin Morphol Blutforsch; 1983; 110(1):98-111. PubMed ID: 6192061
[TBL] [Abstract][Full Text] [Related]
12. Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update.
Rodgers GM
Thromb Haemost; 2009 May; 101(5):806-12. PubMed ID: 19404531
[TBL] [Abstract][Full Text] [Related]
13. Distinction of two pathologic antithrombin III molecules: antithrombin III "Aalborg' and antithrombin III "Budapest'.
Sørensen PJ; Sas G; Petó I; Blaskó G; Kremmer T; Samu A
Thromb Res; 1982 May; 26(3):211-9. PubMed ID: 7112514
[TBL] [Abstract][Full Text] [Related]
14. An antithrombin III assay based on factor Xa inhibition provides a more reliable test to identify congenital antithrombin III deficiency than an assay based on thrombin inhibition.
Demers C; Henderson P; Blajchman MA; Wells MJ; Mitchell L; Johnston M; Ofosu FA; Fernandez-Rachubinski F; Andrew M; Hirsh J
Thromb Haemost; 1993 Mar; 69(3):231-5. PubMed ID: 8470046
[TBL] [Abstract][Full Text] [Related]
15. Inhibition of thrombin by antithrombin III and heparin cofactor II in vivo.
Liu L; Dewar L; Song Y; Kulczycky M; Blajchman MA; Fenton JW; Andrew M; Delorme M; Ginsberg J; Preissner KT
Thromb Haemost; 1995 Mar; 73(3):405-12. PubMed ID: 7545318
[TBL] [Abstract][Full Text] [Related]
16. Prothrombin fragment 1 + 2, thrombin-antithrombin III-complexes and fibrinopeptide A in spontaneously clotting whole blood in vitro. Effects of heparin addition and antithrombin III deficiency.
Herren T; Straub PW; Haeberli A
Thromb Haemost; 1994 Jan; 71(1):49-53. PubMed ID: 8165646
[TBL] [Abstract][Full Text] [Related]
17. Antithrombin III deficiency: clinical aspects.
Nagy I
Haematologia (Budap); 1984; 17(1):87-91. PubMed ID: 6724356
[TBL] [Abstract][Full Text] [Related]
18. Antithrombin III molecular variants with defective binding to heparin or to serine proteases: evidence of two different abnormal patterns identified by crossed immunoelectrofocusing.
Leone G; De Stefano V; Ferrelli R; Teofili L; Tengborn L; Vahtera E; Bizzi B
Thromb Haemost; 1988 Aug; 60(1):8-12. PubMed ID: 3187949
[TBL] [Abstract][Full Text] [Related]
19. Heparin cofactor activities in a family with hereditary antithrombin III deficiency: evidence for a second heparin cofactor in human plasma.
Griffith MJ; Carraway T; White GC; Dombrose FA
Blood; 1983 Jan; 61(1):111-8. PubMed ID: 6184096
[TBL] [Abstract][Full Text] [Related]
20. A new familial variant of antithrombin III: 'antithrombin III Paris'.
Wolf M; Boyer C; Lavergne JM; Larrieu MJ
Br J Haematol; 1982 Jun; 51(2):285-95. PubMed ID: 7082587
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
