147 related articles for article (PubMed ID: 3272307)
1. [Hereditary abnormalities of antithrombin III in patients with recurrent thrombophlebitis].
Bekić-Kaluza S; Rezaković D; Musa M
Med Arh; 1986; 40(1-2):51-3. PubMed ID: 3272307
[No Abstract] [Full Text] [Related]
2. Familial antithrombin III deficiency.
Winter JH; Fenech A; Ridley W; Bennett B; Cumming AM; Mackie M; Douglas AS
Q J Med; 1982; 51(204):373-95. PubMed ID: 7156320
[TBL] [Abstract][Full Text] [Related]
3. [Comparative studies of the antithrombin III level and plasminogen activator activity in patients with thrombophlebitis].
Tymiński W; Czestochowska E; Swiecicki P
Pol Tyg Lek; 1985 Oct; 40(43):1202-4. PubMed ID: 4088936
[No Abstract] [Full Text] [Related]
4. Familial functional antithrombin III deficiency.
Sørensen PJ; Dyerberg J; Stoffersen E; Jensen MK
Scand J Haematol; 1980 Feb; 24(2):105-9. PubMed ID: 7375809
[TBL] [Abstract][Full Text] [Related]
5. [Thrombosis patients with familial antithrombin-III deficiency treated with heparin and antithrombin].
Brandt P
Ugeskr Laeger; 1981; 143(34):2145-8. PubMed ID: 7281335
[No Abstract] [Full Text] [Related]
6. [Diagnosis of thrombophilia - hereditary deficiency of antithrombin III].
Al'pidovskiĭ VK; Lagutina NIa; Fedulova GA; Gerasimov AA
Probl Gematol Pereliv Krovi; 1982 Mar; 27(3):51-5. PubMed ID: 6806802
[No Abstract] [Full Text] [Related]
7. [A family with venous thrombosis and hereditary antithrombin III deficiency].
Michiels JJ; van Vliet HD
Ned Tijdschr Geneeskd; 1986 Jan; 130(1):28-31. PubMed ID: 3951576
[No Abstract] [Full Text] [Related]
8. The prevalence of hereditary antithrombin-III deficiency in patients with a history of venous thromboembolism.
Vikydal R; Korninger C; Kyrle PA; Niessner H; Pabinger I; Thaler E; Lechner K
Thromb Haemost; 1985 Dec; 54(4):744-5. PubMed ID: 4089808
[TBL] [Abstract][Full Text] [Related]
9. A functional abnormal antithrombin III (AT III) deficiency: AT III Charleville.
Aiach M; Nora M; Fiessinger JN; Roncato M; François D; Gelas MA
Thromb Res; 1985 Sep; 39(5):559-70. PubMed ID: 4082101
[TBL] [Abstract][Full Text] [Related]
10. Purification and partial characterization of a hereditary abnormal antithrombin III fraction of a patient with recurrent thrombophlebitis.
Tran TH; Bounameaux H; Bondeli C; Honkanen H; Marbet GA; Duckert F
Thromb Haemost; 1980 Oct; 44(2):87-91. PubMed ID: 7455996
[No Abstract] [Full Text] [Related]
11. Antithrombin III Toyama: a hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitis.
Sakuragawa N; Takahashi K; Kondo S; Koide T
Thromb Res; 1983 Jul; 31(2):305-17. PubMed ID: 6636045
[TBL] [Abstract][Full Text] [Related]
12. [The genetics of thrombosis].
Girolami A; Simioni P; Zanardi S; Coser E; Signora S
Haematologica; 1991 Jun; 76 Suppl 3():249-60. PubMed ID: 1836447
[No Abstract] [Full Text] [Related]
13. Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.
Michiels JJ; van der Luit L; van Vliet HH; Jochmans K; Lissens W
Thromb Res; 1995 May; 78(3):251-4. PubMed ID: 7631305
[No Abstract] [Full Text] [Related]
14. Antithrombin III deficiency in a Romanian family. Pathogenic role of concomitantly increased plasma level of clotting factors VII and X.
Cucuianu M; Comes L; Roman S; Boeru A
Med Interne; 1984; 22(1):13-7. PubMed ID: 6710043
[TBL] [Abstract][Full Text] [Related]
15. [Congenital deficiency of antithrombin III].
Finazzi G; Barbui T
Haematologica; 1990; 75 Suppl 2():6-13. PubMed ID: 2201606
[No Abstract] [Full Text] [Related]
16. [Plasma antithrombin III activity in patients with pulmonary thromboembolism].
Vertun B; Filipecki S; Szczepański M; Wawrzyńska L; Rózycka J
Pol Tyg Lek; 1992 Aug 18-31; 47(34-35):726-9. PubMed ID: 1488357
[TBL] [Abstract][Full Text] [Related]
17. [Severe pulmonary embolism and recurrent thrombophlebitis caused by hereditary antithrombin III deficiency].
Rey JL; Delobel J; Claisse JF; Quiret JC; Bor P; Bernasconi P
Arch Mal Coeur Vaiss; 1979 Aug; 72(8):919-23. PubMed ID: 115439
[TBL] [Abstract][Full Text] [Related]
18. A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis.
Grundy CB; Holding S; Millar DS; Kakkar VV; Cooper DN
Hum Genet; 1992 Mar; 88(6):707-8. PubMed ID: 1551681
[No Abstract] [Full Text] [Related]
19. Inherited hypercoagulable states in children.
Whitlock JA; Janco RL; Phillips JA
Am J Pediatr Hematol Oncol; 1989; 11(2):170-3. PubMed ID: 2526603
[TBL] [Abstract][Full Text] [Related]
20. Familial deficiency of antithrombin III: evidence for heterogeneity existing within the family.
d'Souza S; Ekert H
Aust N Z J Med; 1984 Dec; 14(6):835-40. PubMed ID: 6598052
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
