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25. Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene. Picard V; Nowak-Göttl U; Biron-Andreani C; Fouassier M; Frere C; Goualt-Heilman M; de Maistre E; Regina S; Rugeri L; Ternisien C; Trichet C; Vergnes C; Aiach M; Alhenc-Gelas M Hum Mutat; 2006 Jun; 27(6):600. PubMed ID: 16705712 [TBL] [Abstract][Full Text] [Related]
26. Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiency. Cieśla M; Wypasek E; Corral J; Alhenc-Gelas M; Undas A Blood Coagul Fibrinolysis; 2015 Jan; 26(1):95-7. PubMed ID: 25083771 [TBL] [Abstract][Full Text] [Related]
27. Familial antithrombin III deficiency: its natural history, genetics, diagnosis and treatment. Cosgriff TM; Bishop DT; Hershgold EJ; Skolnick MH; Martin BA; Baty BJ; Carlson KS Medicine (Baltimore); 1983 Jul; 62(4):209-20. PubMed ID: 6877092 [No Abstract] [Full Text] [Related]
28. Antithrombin III: summary of first database update. Lane DA; Olds RJ; Thein SL Nucleic Acids Res; 1994 Sep; 22(17):3556-9. PubMed ID: 7937056 [TBL] [Abstract][Full Text] [Related]
29. Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin alpha-helix D molecular pathology. Steiner M; Steiner B; Rolfs A; Wangnick M; Burstein C; Freund M; Schuff-Werner P Ann Hematol; 2005 Jan; 84(1):56-8. PubMed ID: 15309521 [No Abstract] [Full Text] [Related]
33. Cerebral infarction in a heterozygote with variant antithrombin III. Arima T; Motomura M; Nishiura Y; Tsujihata M; Okajima K; Abe H; Nagataki S Stroke; 1992 Dec; 23(12):1822-5. PubMed ID: 1448834 [TBL] [Abstract][Full Text] [Related]
34. A novel antithrombin gene mutation: slippage and mispairing as a mechanism of genetic disease. Fitches AC; May SJ; Olds RJ Pathology; 1996 Nov; 28(4):339-42. PubMed ID: 9007953 [TBL] [Abstract][Full Text] [Related]
35. Familial antithrombin III deficiency. O'Donnell J; Day AJ; Snell AP N Z Med J; 1985 Jun; 98(781):481-3. PubMed ID: 3859772 [No Abstract] [Full Text] [Related]
36. [Discrepancy of biological antithrombins measured as progressive activity and heparin cofactor in a family with antithrombin III deficiency]. Matsuo T; Ohoki Y; Matsuo O Rinsho Byori; 1982 Sep; 30(9):1033-6. PubMed ID: 7176137 [No Abstract] [Full Text] [Related]
37. [A family with an estrogen-related thrombotic tendency and hereditary deficiency on antithrombin]. Brandt P Ugeskr Laeger; 1981; 143(34):2141-5. PubMed ID: 7281334 [No Abstract] [Full Text] [Related]
38. [Thrombophilia in a patient with congenital deficiency of AT III]. Miljić P; Colović M; Stanojević M; Elezović I; Bosković D Srp Arh Celok Lek; 1994; 122(11-12):344-6. PubMed ID: 17974415 [TBL] [Abstract][Full Text] [Related]
39. A novel mutation in the SerpinC1 gene presenting as unprovoked neonatal cerebral sinus venous thrombosis in a kindred. Kumar R; Moharir M; Yau I; Williams S Pediatr Blood Cancer; 2013 Jan; 60(1):133-6. PubMed ID: 22997155 [TBL] [Abstract][Full Text] [Related]
40. [Antithrombin-III levels in patients with acute cerebrovascular disease]. Han ZY Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1988 Feb; 21(1):41-2, 63. PubMed ID: 3402275 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]