These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
119 related articles for article (PubMed ID: 7579427)
1. Two common mutations causing factor XI deficiency in Ashkenazi Jews may point to a European origin. Zoossmann-Diskin A Blood; 1995 Oct; 86(8):3267-8. PubMed ID: 7579427 [No Abstract] [Full Text] [Related]
2. One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews. Shpilberg O; Peretz H; Zivelin A; Yatuv R; Chetrit A; Kulka T; Stern C; Weiss E; Seligsohn U Blood; 1995 Jan; 85(2):429-32. PubMed ID: 7811996 [TBL] [Abstract][Full Text] [Related]
3. The two common mutations causing factor XI deficiency in Jews stem from distinct founders: one of ancient Middle Eastern origin and another of more recent European origin. Peretz H; Mulai A; Usher S; Zivelin A; Segal A; Weisman Z; Mittelman M; Lupo H; Lanir N; Brenner B; Shpilberg O; Seligsohn U Blood; 1997 Oct; 90(7):2654-9. PubMed ID: 9326232 [TBL] [Abstract][Full Text] [Related]
4. Molecular genetics aspects of factor XI deficiency and Glanzmann thrombasthenia. Seligsohn U; Peretz H Haemostasis; 1994; 24(2):81-5. PubMed ID: 7959366 [TBL] [Abstract][Full Text] [Related]
5. Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations. Asakai R; Chung DW; Ratnoff OD; Davie EW Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7667-71. PubMed ID: 2813350 [TBL] [Abstract][Full Text] [Related]
6. Factor XI deficiency in Ashkenazi Jews in Israel. Asakai R; Chung DW; Davie EW; Seligsohn U N Engl J Med; 1991 Jul; 325(3):153-8. PubMed ID: 2052060 [TBL] [Abstract][Full Text] [Related]
7. Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews. Peretz H; Salomon O; Mor-Cohen R; Usher S; Zucker M; Zivelin A; Seligsohn U J Thromb Haemost; 2013 Apr; 11(4):724-30. PubMed ID: 23332144 [TBL] [Abstract][Full Text] [Related]
8. Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews. Goldstein DB; Reich DE; Bradman N; Usher S; Seligsohn U; Peretz H Am J Hum Genet; 1999 Apr; 64(4):1071-5. PubMed ID: 10090892 [TBL] [Abstract][Full Text] [Related]
10. Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data. Colombo R Am J Hum Genet; 2000 Feb; 66(2):692-7. PubMed ID: 10677327 [TBL] [Abstract][Full Text] [Related]
11. Review: Factor XI deficiency: review and management in pregnant women. Martín-Salces M; Jimenez-Yuste V; Alvarez MT; Quintana M; Hernández-Navarro F Clin Appl Thromb Hemost; 2010 Apr; 16(2):209-13. PubMed ID: 19049995 [TBL] [Abstract][Full Text] [Related]
12. Four novel FXI gene mutations in three factor XI- deficient patients. de Raucourt E; de Mazancourt P; Quélin F Blood Coagul Fibrinolysis; 2008 Apr; 19(3):240-2. PubMed ID: 18388506 [TBL] [Abstract][Full Text] [Related]
13. Factor XI Deficiency. Duga S; Salomon O Semin Thromb Hemost; 2009 Jun; 35(4):416-25. PubMed ID: 19598070 [TBL] [Abstract][Full Text] [Related]
14. Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians. Zadra G; Asselta R; Tenchini ML; Castaman G; Seligsohn U; Mannucci PM; Duga S Haematologica; 2008 May; 93(5):715-21. PubMed ID: 18387979 [TBL] [Abstract][Full Text] [Related]
15. Factor XI: a review of its biochemistry and deficiency. Kitchens CS Semin Thromb Hemost; 1991 Jan; 17(1):55-72. PubMed ID: 2047881 [TBL] [Abstract][Full Text] [Related]
16. Severe factor XI deficiency in the Abruzzo region of Italy is associated to different FXI gene mutations. Castaman G; Giacomelli SH; Dragani A; Iuliani O; Duga S; Rodeghiero F Haematologica; 2008 Jun; 93(6):957-8. PubMed ID: 18515884 [No Abstract] [Full Text] [Related]
17. Severe factor XI deficiency caused by compound heterozygosity. Dai L; Mitchell M; Carson P; Creagh D; Cutler J; Savidge G; Alhaq A Br J Haematol; 2004 Jun; 125(6):817-8. PubMed ID: 15180874 [No Abstract] [Full Text] [Related]