94 related articles for article (PubMed ID: 11154130)
1. Antithrombin niigata: a novel missense mutation (Thr194-Ile) of the antithrombin gene results in type I deficiency.
Fuse I; Ozawa T; Higuchi W; Aizawa Y
Thromb Haemost; 2000 Dec; 84(6):1126. PubMed ID: 11154130
[No Abstract] [Full Text] [Related]
2. [Type I antithrombin deficiency due to 13389G deletion in antithrombin gene].
Fu Q; Xu X; Ding Q; Hu Y; Wang X; Wang H
Zhonghua Xue Ye Xue Za Zhi; 2002 Nov; 23(11):588-90. PubMed ID: 12482344
[TBL] [Abstract][Full Text] [Related]
3. [Type I hereditary antithrombin deficiency due to C2757T heterozygotic mutation in antithrombin gene].
Zhou RF; Dai Q; Fu QH; Wang WB; Xue S; Ding QL; Hu YQ; Wang XF; Wang HL
Zhonghua Yi Xue Za Zhi; 2005 Jun; 85(23):1640-2. PubMed ID: 16185535
[No Abstract] [Full Text] [Related]
4. Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency.
Ozawa T; Takikawa Y; Niiya K; Fujiwara T; Suzuki K; Sato S; Sakuragawa N
Thromb Haemost; 1997 Feb; 77(2):403. PubMed ID: 9157604
[No Abstract] [Full Text] [Related]
5. 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]
6. Identification of the novel signal peptide mutation, antithrombin-Siriraj causes type-I antithrombin deficiency in thai patients.
Chinthammitr Y; Chinchang W; Ruchutrakool T; Viprakasit V
Thromb Haemost; 2005 Sep; 94(3):678-9. PubMed ID: 16268490
[No Abstract] [Full Text] [Related]
7. Characterization of two novel mutations of the antithrombin gene observed in Japanese thrombophilic patients.
Kurihara M; Watanabe K; Inoue S; Wada Y; Ono M; Wakiyama M; Iida H; Kinoshita S; Hamasaki N
Thromb Res; 2005; 115(5):351-8. PubMed ID: 15733967
[TBL] [Abstract][Full Text] [Related]
8. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
Mahajan A; Chavali S; Kabra M; Chowdhury MR; Bharadwaj D
Haematologica; 2004 Dec; 89(12):1498-503. PubMed ID: 15590401
[TBL] [Abstract][Full Text] [Related]
9. [A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].
Zhang FH; Ding QL; Wu JS; Zhou RF; Wang XF; Xu XC
Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):598-601. PubMed ID: 17278425
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene.
Espinós C; Casaña P; Haya S; Cid AR; Aznar JA
Haematologica; 2003 Feb; 88(2):235-6. PubMed ID: 12604421
[No Abstract] [Full Text] [Related]
12. Factor IX Denver, ASN 346-->ASP mutation resulting in a dysfunctional protein with defective factor VIIIa interaction.
Lefkowitz JB; Nuss R; Haver T; Jacobson L; Thompson AR; Manco-Johnson M
Thromb Haemost; 2001 Sep; 86(3):862-70. PubMed ID: 11583320
[TBL] [Abstract][Full Text] [Related]
13. Identification of six novel mutations in type I antithrombin deficient Italian families.
Di Perna P; Vecchione G; D'Andrea G; Scenna G; Brancaccio V; Margaglione M
Haematologica; 2004 Jan; 89(1):117-8. PubMed ID: 14754620
[No Abstract] [Full Text] [Related]
14. A recurrent deletion in the antithrombin gene, AT106-108(-6 bp), identified by DNA heteroduplex detection.
Olds RJ; Lane DA; Beresford CH; Abildgaard U; Hughes PM; Thein SL
Genomics; 1993 Apr; 16(1):298-9. PubMed ID: 8486379
[No Abstract] [Full Text] [Related]
15. A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia.
Tarantino MD; Curtis SM; Johnson GS; Waye JS; Blajchman MA
Am J Hematol; 1999 Feb; 60(2):126-9. PubMed ID: 9929104
[TBL] [Abstract][Full Text] [Related]
16. Fibrinogen Tolaga Bay: a novel gammaAla341Val mutation causing hypofibrinogenaemia.
Davis RL; Brennan SO
Thromb Haemost; 2007 Nov; 98(5):1136-8. PubMed ID: 18000621
[No Abstract] [Full Text] [Related]
17. X-linked thrombophilia with a mutant factor IX (factor IX Padua).
Simioni P; Tormene D; Tognin G; Gavasso S; Bulato C; Iacobelli NP; Finn JD; Spiezia L; Radu C; Arruda VR
N Engl J Med; 2009 Oct; 361(17):1671-5. PubMed ID: 19846852
[TBL] [Abstract][Full Text] [Related]
18. [A heterozygous point mutation G13328A in antithrombin gene causes thrombosis].
Zhou RF; Shi GC; Fu QH; Wang WB; Xie S; Dai J; Ding QL; Hu YQ; Wang XF; Deng WW; Wang HL
Zhonghua Xue Ye Xue Za Zhi; 2005 Nov; 26(11):661-4. PubMed ID: 16620552
[TBL] [Abstract][Full Text] [Related]
19. Molecular genotyping of the Italian cohort of patients with hemophilia B.
Belvini D; Salviato R; Radossi P; Pierobon F; Mori P; Castaldo G; Tagariello G;
Haematologica; 2005 May; 90(5):635-42. PubMed ID: 15921378
[TBL] [Abstract][Full Text] [Related]
20. Novel missense mutation in the coagulation factor IX catalytic domain associated with severe haemophilia B--Factor IXDelhi.
Mahajan A; Sharma A; Chavali S; Kabra M; Chowdhury MR; Srinivasan N; Bharadwaj D
Haemophilia; 2004 Sep; 10(5):550-2. PubMed ID: 15357782
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]