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Journal Abstract Search
106 related items for PubMed ID: 7176889
1. [Characterization of a family with hereditary antithrombin III deficiency type I]. Lögering HL, Paar D. Med Welt; 1982 Nov 26; 33(47):1705-7. PubMed ID: 7176889 [No Abstract] [Full Text] [Related]
2. 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 17; 54(4):744-5. PubMed ID: 4089808 [Abstract] [Full Text] [Related]
3. [Familial deficiency of antithrombin III]. Coget JM, Dendien-Bernard S, Dupuis-Cuny C. Phlebologie; 1987 Dec 17; 40(2):381-91. PubMed ID: 3615614 [Abstract] [Full Text] [Related]
4. Clinical and genetic aspects of antithrombin III deficiency. Halal F, Quenneville G, Laurin S, Loulou G. Am J Med Genet; 1983 Apr 17; 14(4):737-50. PubMed ID: 6846404 [No Abstract] [Full Text] [Related]
6. [Familial antithrombin III deficiency and thromboembolic disease]. Watel A, Goudemand J, Zandecki M, Laisne C, Bertrand ME, Cosson A. Lille Med; 1978 Oct 17; 23(8):555-60. PubMed ID: 723422 [No Abstract] [Full Text] [Related]
7. Familial antithrombin III deficiency. O'Donnell J, Day AJ, Snell AP. N Z Med J; 1985 Jun 26; 98(781):481-3. PubMed ID: 3859772 [No Abstract] [Full Text] [Related]
9. Inherited antithrombin III deficiency in an Italian family, associated with venous and arterial thrombosis. Candrina R, Coppini A, Salvi A, Zuccato F, Del Bono R, Giustina G. Haematologica; 1985 Jun 26; 70(5):399-404. PubMed ID: 3937775 [No Abstract] [Full Text] [Related]
10. Antithrombin-III (AT-III) deficiency spanning four generations. Mazza JJ, Mueller-Rizner NJ, Roberts RC. Thromb Haemost; 1991 Dec 02; 66(6):737-8. PubMed ID: 1796421 [No Abstract] [Full Text] [Related]
12. [Antithrombin III, the most important inhibitor of hemostasis. Physiology and clinical aspects]. Neubauer M, Ramschak H, Lanzer G. Wien Med Wochenschr; 1986 Nov 30; 136(21-22):560-2. PubMed ID: 3825161 [Abstract] [Full Text] [Related]
13. Replacement therapy in patients with hereditary antithrombin III deficiency. Menache D. Semin Hematol; 1991 Jan 30; 28(1):31-8. PubMed ID: 2017690 [No Abstract] [Full Text] [Related]
14. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin. Brouwer JL, Lijfering WM, Ten Kate MK, Kluin-Nelemans HC, Veeger NJ, van der Meer J. Thromb Haemost; 2009 Jan 30; 101(1):93-9. PubMed ID: 19132194 [Abstract] [Full Text] [Related]
15. Role of antithrombin III as a regulator of in vivo coagulation. Bauer KA, Rosenberg RD. Semin Hematol; 1991 Jan 30; 28(1):10-8. PubMed ID: 2017686 [No Abstract] [Full Text] [Related]
16. [New variants of congenital antithrombin III deficiency]. Petö I, Bánhegyi D, Blaskó G, Sas G. Orv Hetil; 1980 Jun 22; 121(25):1507-9. PubMed ID: 7454260 [No Abstract] [Full Text] [Related]
17. [Molecular anomalies of coagulation inhibitors]. Aiach M. Nouv Rev Fr Hematol (1978); 1993 Jun 22; 35(3):265-6. PubMed ID: 8337141 [No Abstract] [Full Text] [Related]
18. A common point mutation producing type 1A antithrombin III deficiency: AT129 CGA to TGA (Arg to Stop). Olds RJ, Lane DA, Ireland H, Finazzi G, Barbui T, Abildgaard U, Girolami A, Thein SL. Thromb Res; 1991 Dec 01; 64(5):621-5. PubMed ID: 1808766 [No Abstract] [Full Text] [Related]
19. Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases. Finazzi G, Caccia R, Barbui T. Thromb Haemost; 1987 Dec 18; 58(4):1094. PubMed ID: 3328320 [No Abstract] [Full Text] [Related]
20. [Factor XII (Hageman factor) deficiency: a risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboembolism and myocardial infarction]. Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M. Wien Med Wochenschr; 1993 Dec 18; 143(2):43-50. PubMed ID: 8488686 [Abstract] [Full Text] [Related] Page: [Next] [New Search]