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Items: 1 to 20 of 104

1.

Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiency.

Salomon O, Zivelin A, Livnat T, Dardik R, Loewenthal R, Avishai O, Steinberg DM, Rosove MH, O'Connell N, Lee CA, Seligsohn U.

Blood. 2003 Jun 15;101(12):4783-8.

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 15;85(2):429-32.

3.

Factor XI Deficiency.

Duga S, Salomon O.

Semin Thromb Hemost. 2009 Jun;35(4):416-25. doi: 10.1055/s-0029-1225764. Review.

PMID:
19598070
4.

Factor XI deficiency in Ashkenazi Jews in Israel.

Asakai R, Chung DW, Davie EW, Seligsohn U.

N Engl J Med. 1991 Jul 18;325(3):153-8.

6.

Factor XI deficiency in humans.

Seligsohn U.

J Thromb Haemost. 2009 Jul;7 Suppl 1:84-7. doi: 10.1111/j.1538-7836.2009.03395.x. Review.

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. doi: 10.1111/jth.12137.

8.

Defective binding of factor XI-N248 to activated human platelets.

Sun MF, Baglia FA, Ho D, Martincic D, Ware RE, Walsh PN, Gailani D.

Blood. 2001 Jul 1;98(1):125-9. Erratum in: Blood. 2007 Dec 15;110(13):4164.

10.

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. doi: 10.3324/haematol.12180.

11.

Acquired antibody to factor XI in a patient with congenital factor XI deficiency.

Stern DM, Nossel HL, Owen J.

J Clin Invest. 1982 Jun;69(6):1270-6.

12.

Factor XI gene mutations in factor XI deficient patients of the Czech Republic.

Castaman G, Giacomelli SH, Habart D, Asselta R, Duga S, Rodeghiero F.

Am J Hematol. 2008 Dec;83(12):916-9. doi: 10.1002/ajh.21286.

14.

Studies on a circulating anticoagulant inhibiting factor XI in a patient with congenital deficiency and carcinoma of the prostate.

Chediak J, Madej-Zevin P, Ratnoff OD, Goldsmith GH Jr, Everson B.

Br J Haematol. 1986 May;63(1):123-33.

PMID:
3486671
15.

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. doi: 10.1097/MBC.0b013e3282f6d256.

PMID:
18388506
16.
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18.

Factor XI activity and factor XI antigen in homozygous and heterozygous factor XI deficiency.

Rimon A, Schiffman S, Feinstein DI, Rapaport SI.

Blood. 1976 Aug;48(2):165-74.

20.

Inherited factor XI deficiency confers no protection against acute myocardial infarction.

Salomon O, Steinberg DM, Dardik R, Rosenberg N, Zivelin A, Tamarin I, Ravid B, Berliner S, Seligsohn U.

J Thromb Haemost. 2003 Apr;1(4):658-61.

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