113 related articles for article (PubMed ID: 7831651)
1. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis.
Chowdhury V; Lane DA; Mille B; Auberger K; Gandenberger-Bachem S; Pabinger I; Olds RJ; Thein SL
Thromb Haemost; 1994 Aug; 72(2):198-202. PubMed ID: 7831651
[TBL] [Abstract][Full Text] [Related]
2. Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.
Kuhle S; Lane DA; Jochmanns K; Male C; Quehenberger P; Lechner K; Pabinger I
Thromb Haemost; 2001 Oct; 86(4):1007-11. PubMed ID: 11686316
[TBL] [Abstract][Full Text] [Related]
3. Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.
Orlando C; Heylen O; Lissens W; Jochmans K
Thromb Res; 2015 Jun; 135(6):1179-85. PubMed ID: 25837307
[TBL] [Abstract][Full Text] [Related]
4. Life-threatening thrombosis in mice with targeted Arg48-to-Cys mutation of the heparin-binding domain of antithrombin.
Dewerchin M; Hérault JP; Wallays G; Petitou M; Schaeffer P; Millet L; Weitz JI; Moons L; Collen D; Carmeliet P; Herbert JM
Circ Res; 2003 Nov; 93(11):1120-6. PubMed ID: 14592998
[TBL] [Abstract][Full Text] [Related]
5. [Homozygous antithrombin type HBS deficiency; a family study].
Guermazi S; Elloumi-ZghaL H; Ben Hassine L; Romani S; Khalfallah N; Abdelhak S; Dellagi K
Pathol Biol (Paris); 2007 Jun; 55(5):256-61. PubMed ID: 17140748
[TBL] [Abstract][Full Text] [Related]
6. Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors.
David D; Ribeiro S; Ferrão L; Gago T; Crespo F
Am J Hematol; 2004 Jun; 76(2):163-71. PubMed ID: 15164384
[TBL] [Abstract][Full Text] [Related]
7. Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate.
Baud O; Picard V; Durand P; Duchemin J; Proulle V; Alhenc-Gelas M; Devictor D; Dreyfus M
J Pediatr; 2001 Nov; 139(5):741-3. PubMed ID: 11713457
[TBL] [Abstract][Full Text] [Related]
8. Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency.
van Boven HH; Reitsma PH; Rosendaal FR; Bayston TA; Chowdhury V; Bauer KA; Scharrer I; Conard J; Lane DA
Thromb Haemost; 1996 Mar; 75(3):417-21. PubMed ID: 8701400
[TBL] [Abstract][Full Text] [Related]
9. [Type I antithrombin deficiency as a cause of arterial and venous thrombosis in a family with severe thrombophilia].
Tóth O; Dávid M; Habon T; Nagy A; Keszthelyi Z; Kovács N; Losonczy H
Orv Hetil; 2005 Oct; 146(41):2121-5. PubMed ID: 16304806
[TBL] [Abstract][Full Text] [Related]
10. "Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.
Simioni P; Scudeller A; Radossi P; Gavasso S; Girolami B; Tormene D; Girolami A
Thromb Haemost; 1996 Mar; 75(3):422-6. PubMed ID: 8701401
[TBL] [Abstract][Full Text] [Related]
11. The molecular basis of antithrombin deficiency in Belgian and Dutch families.
Jochmans K; Lissens W; Seneca S; Capel P; Chatelain B; Meeus P; Osselaer JC; Peerlinck K; Seghers J; Slacmeulder M; Stibbe J; van de Loo J; Vermylen J; Liebaers I; De Waele M
Thromb Haemost; 1998 Sep; 80(3):376-81. PubMed ID: 9759613
[TBL] [Abstract][Full Text] [Related]
12. The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.
Arruda VR; von Zuben PM; Chiaparini LC; Annichino-Bizzacchi JM; Costa FF
Thromb Haemost; 1997 May; 77(5):818-21. PubMed ID: 9184384
[TBL] [Abstract][Full Text] [Related]
13. Hereditary homozygous heparin cofactor II deficiency and the risk of developing venous thrombosis.
Villa P; Aznar J; Vaya A; España F; Ferrando F; Mira Y; Estellés A
Thromb Haemost; 1999 Sep; 82(3):1011-4. PubMed ID: 10494755
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease.
Zöller B; He X; Dahlbäck B
Thromb Haemost; 1995 May; 73(5):743-5. PubMed ID: 7482396
[TBL] [Abstract][Full Text] [Related]
16. Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.
Rossi E; Chiusolo P; Za T; Marietti S; Ciminello A; Leone G; De Stefano V
Thromb Haemost; 2007 Sep; 98(3):695-7. PubMed ID: 17849067
[No Abstract] [Full Text] [Related]
17. Homozygous variant of antithrombin with lack of affinity for heparin: management of severe thrombotic complications associated with intrauterine fetal demise.
Bauters A; Zawadzki C; Bura A; Théry C; Watel A; Subtil D; Aiach M; Emmerich J; Jude B
Blood Coagul Fibrinolysis; 1996 Oct; 7(7):705-10. PubMed ID: 8958394
[TBL] [Abstract][Full Text] [Related]
18. Anticoagulant proteins in childhood venous and arterial thrombosis: a review.
Segel GB; Francis CA
Blood Cells Mol Dis; 2000 Oct; 26(5):540-60. PubMed ID: 11112387
[TBL] [Abstract][Full Text] [Related]
19. Acute mesenteric and aortic thrombosis associated with antithrombin deficiency: a rare occurrence.
Calcaterra D; Martin JT; Ferneini AM; De Natale RW
Ann Vasc Surg; 2010 Apr; 24(3):415.e5-7. PubMed ID: 19932950
[TBL] [Abstract][Full Text] [Related]
20. Antithrombin and its deficiency states.
Lane DA; Olds RR; Thein SL
Blood Coagul Fibrinolysis; 1992 Jun; 3(3):315-41. PubMed ID: 1643210
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
