146 related articles for article (PubMed ID: 8735803)
21. Identification of eight point mutations in protein S deficiency type I--analysis of 15 pedigrees.
Gómez E; Poort SR; Bertina RM; Reitsma PH
Thromb Haemost; 1995 May; 73(5):750-5. PubMed ID: 7482398
[TBL] [Abstract][Full Text] [Related]
22. Genetic analysis in Japanese kindreds of congenital type I antithrombin deficiency causing thrombosis.
Nakahara Y; Tsuji H; Nakagawa K; Masuda H; Kitamura H; Nishimura H; Kasahara T; Sugano T; Sawada S; Nakagawa M
Thromb Haemost; 1997 Apr; 77(4):616-9. PubMed ID: 9134630
[TBL] [Abstract][Full Text] [Related]
23. Novel mutation (E113X) of antithrombin III gene (AT3) in a woman with gestational recurrent thrombosis.
Yamada H; Hoshi N; Kato EH; Ebina Y; Kishida T; Sagawa T; Matsuno K; Fujimoto S
Am J Med Genet; 2000 Apr; 91(5):348-50. PubMed ID: 10766996
[TBL] [Abstract][Full Text] [Related]
24. [Molecular basis of hereditary antithrombin defects in 10 Czech families].
Hrachovinová I; Habart D; Salaj P; Matysková M; Vorlová Z
Cas Lek Cesk; 2000 Sep; 139(19):596-8. PubMed ID: 11192751
[TBL] [Abstract][Full Text] [Related]
25. Antithrombin cambridge II (Ala384Ser): clinical, functional and haplotype analysis of 18 families.
Perry DJ; Daly ME; Tait RC; Walker ID; Brown K; Beauchamp NJ; Preston FE; Gyde H; Harper PL; Carrell RW
Thromb Haemost; 1998 Feb; 79(2):249-53. PubMed ID: 9493570
[TBL] [Abstract][Full Text] [Related]
26. Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations.
Long GL; Tomczak JA; Rainville IR; Dreyfus M; Schramm W; Schwarz HP
Thromb Haemost; 1994 Oct; 72(4):526-33. PubMed ID: 7878626
[TBL] [Abstract][Full Text] [Related]
27. [Antithrombin deficiency due to heterozygous antithrombin gene mutation and a pedigree study].
Ye X; Feng Y; Jin PP; Zhou XH; Ding QL; Wang XF
Zhonghua Xue Ye Xue Za Zhi; 2007 Sep; 28(9):587-9. PubMed ID: 18246812
[TBL] [Abstract][Full Text] [Related]
28. Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutation.
De Siervi A; Rossetti MV; Parera VE; Astrin KH; Aizencang GI; Glass IA; Batlle AM; Desnick RJ
Am J Med Genet; 1999 Oct; 86(4):366-75. PubMed ID: 10494093
[TBL] [Abstract][Full Text] [Related]
29. Molecular basis of antithrombin deficiency.
Luxembourg B; Delev D; Geisen C; Spannagl M; Krause M; Miesbach W; Heller C; Bergmann F; Schmeink U; Grossmann R; Lindhoff-Last E; Seifried E; Oldenburg J; Pavlova A
Thromb Haemost; 2011 Apr; 105(4):635-46. PubMed ID: 21264449
[TBL] [Abstract][Full Text] [Related]
30. [Cerebrovascular accidents with familial antithrombin III deficiency--gene analysis study].
Tsukahara S; Iizuka T; Suzuki N; Sakai F
Rinsho Shinkeigaku; 2002 Mar; 42(3):207-11. PubMed ID: 12474289
[TBL] [Abstract][Full Text] [Related]
31. Screening for mutations in the antithrombin III gene causing recurrent venous thrombosis by single-strand conformation polymorphism analysis.
Millar DS; Lopez A; White D; Abraham G; Laursen B; Holding S; Reverter JC; Reynaud J; Martinowitz U; Hayes JP
Hum Mutat; 1993; 2(4):324-6. PubMed ID: 8401542
[No Abstract] [Full Text] [Related]
32. Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds.
Sacks SH; Old JM; Reeders ST; Weatherall DJ; Douglas AS; Winter JH; Rizza CR
J Med Genet; 1988 Jan; 25(1):20-4. PubMed ID: 3162535
[TBL] [Abstract][Full Text] [Related]
33. Molecular analysis and genotype-phenotype correlation in patients with antithrombin deficiency from Southern Italy.
Castaldo G; Cerbone AM; Guida A; Tandurella I; Ingino R; Tufano A; Ceglia C; Di Minno MN; Ruocco AL; Di Minno G
Thromb Haemost; 2012 Apr; 107(4):673-80. PubMed ID: 22398878
[TBL] [Abstract][Full Text] [Related]
34. Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene.
Soria JM; Berg LP; Fontcuberta J; Kakkar VV; Estivill X; Cooper DN; Sala N
Thromb Haemost; 1996 Jun; 75(6):870-6. PubMed ID: 8822578
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. Genetic analysis should be included in clinical practice when screening for antithrombin deficiency.
Zeng W; Tang L; Jian XR; Li YQ; Guo T; Wang QY; Liu H; Wu YY; Cheng ZP; Hu B; Lu X; Yu JM; Deng J; Wang HF; Sun CY; Yang Y; Hu Y
Thromb Haemost; 2015 Feb; 113(2):262-71. PubMed ID: 25298121
[TBL] [Abstract][Full Text] [Related]
37. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
Miyata T; Zheng YZ; Sakata T; Tsushima N; Kato H
Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
[TBL] [Abstract][Full Text] [Related]
38. Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families.
Andersen BD; Bisgaard ML; Lind B; Philips M; Villoutreix B; Thorsen S
Thromb Haemost; 2001 Dec; 86(6):1392-9. PubMed ID: 11776305
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Ectopic transcript analysis in human antithrombin deficiency.
Perry DJ
Blood Coagul Fibrinolysis; 1995 Sep; 6(6):531-6. PubMed ID: 7578894
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]