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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1965 1
1966 1
1968 3
1971 2
1973 1
1977 3
1979 3
1980 2
1981 1
1982 1
1983 2
1984 5
1985 1
1986 5
1987 4
1988 3
1989 4
1990 2
1991 1
1992 3
1993 4
1994 3
1996 1
1998 4
1999 3
2000 3
2001 3
2002 6
2003 2
2004 2
2005 2
2006 7
2007 5
2008 8
2009 2
2010 3
2011 3
2012 4
2013 5
2014 3
2015 4
2016 6
2017 5
2018 7
2019 9
2020 7
2021 7
2022 7
2023 12
2024 1

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171 results

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Page 1
Congenital factor XI deficiency: an update.
Duga S, Salomon O. Duga S, et al. Semin Thromb Hemost. 2013 Sep;39(6):621-31. doi: 10.1055/s-0033-1353420. Epub 2013 Aug 8. Semin Thromb Hemost. 2013. PMID: 23929304 Review.
Severe factor XI (FXI) deficiency is an injury-related bleeding disorder, common in Ashkenazi Jews (with two mutations prevailing), but rare worldwide (with heterogeneous mutations). ...The acceptance of FXI as a risk factor for thrombosis is a new con …
Severe factor XI (FXI) deficiency is an injury-related bleeding disorder, common in Ashkenazi Jews (with two mutations …
Congenital factor XI deficiency and risk of heart failure in humans.
Lova A, Pagán J, de la Morena G, Vázquez DJ, Cerezo-Manchado JJ, Bravo-Pérez C, Miñano A, Tomás A, Vicente V, Lozano ML, Corral J, de la Morena-Barrio ME. Lova A, et al. J Thromb Haemost. 2023 Sep;21(9):2626-2629. doi: 10.1016/j.jtha.2023.06.013. Epub 2023 Jun 17. J Thromb Haemost. 2023. PMID: 37336435 No abstract available.
Congenital factor XI deficiency with multiple tooth extractions (Case report).
Kato T, Yamada M, Watanabe T, Yamanaka S, Fukuhara S, Nakao K. Kato T, et al. Exp Ther Med. 2023 Sep 15;26(5):509. doi: 10.3892/etm.2023.12208. eCollection 2023 Nov. Exp Ther Med. 2023. PMID: 37840565 Free PMC article.
Congenital factor XI deficiency (CFXI) is a rare blood disorder that occurs in one of every one million individuals. ...
Congenital factor XI deficiency (CFXI) is a rare blood disorder that occurs in one of every one million individu …
Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families.
Dorgalaleh A, Gholaminezhad M, Shiravand Y, Naderi M, Safa M. Dorgalaleh A, et al. Blood Coagul Fibrinolysis. 2019 Dec;30(8):409-412. doi: 10.1097/MBC.0000000000000862. Blood Coagul Fibrinolysis. 2019. PMID: 31644447
: Congenital factor XI (FXI) deficiency is a mild trauma-related bleeding disorder with estimated worldwide prevalence of one per 1 million. ...FXI deficiency is a mild bleeding disorder that is caused by heterogeneous molecular defects....
: Congenital factor XI (FXI) deficiency is a mild trauma-related bleeding disorder with estimated worldwide prev …
Combined Congenital Hypodysfibrinogemia and Factor XI Deficiency in a Chinese Family.
Peng Y, Nie L, Qin C, Wan L, Zhou P. Peng Y, et al. Acta Haematol. 2020;143(5):472-477. doi: 10.1159/000505012. Epub 2020 Jan 24. Acta Haematol. 2020. PMID: 31982874
Both congenital hypodysfibrinogenemia and factor XI deficiency are rare coagulopathies caused by mutations within the fibrinogen and F11 genes, respectively. To investigate the pathogenesis of combined congenital hypodysfibrinogenemia with fa …
Both congenital hypodysfibrinogenemia and factor XI deficiency are rare coagulopathies caused by mutations withi …
Clinical Evaluation of Factor XIa Inhibitor Drugs: JACC Review Topic of the Week.
Harrington J, Piccini JP, Alexander JH, Granger CB, Patel MR. Harrington J, et al. J Am Coll Cardiol. 2023 Feb 28;81(8):771-779. doi: 10.1016/j.jacc.2022.11.057. J Am Coll Cardiol. 2023. PMID: 36813377 Free article. Review.
Factor XI/XIa (FXI/FXIa) represents a potential target for improved precision in anticoagulation because it is involved primarily in thrombus formation and plays a much smaller role in clotting and hemostasis. ...This theory is supported by observational data showin …
Factor XI/XIa (FXI/FXIa) represents a potential target for improved precision in anticoagulation because it is involved primar …
Factor XI and factor XII as targets for new anticoagulants.
Weitz JI. Weitz JI. Thromb Res. 2016 May;141 Suppl 2:S40-5. doi: 10.1016/S0049-3848(16)30363-2. Thromb Res. 2016. PMID: 27207423 Review.
Thus, thrombosis is attenuated in mice deficient in factor XII or factor XI and patients with congenital factor XII deficiency do not bleed and those with factor XI deficiency rarely have spontaneous bleeding. ...Ther …
Thus, thrombosis is attenuated in mice deficient in factor XII or factor XI and patients with congenital fact …
Congenital factor XI deficiency in a domestic shorthair cat.
Troxel MT, Brooks MB, Esterline ML. Troxel MT, et al. J Am Anim Hosp Assoc. 2002 Nov-Dec;38(6):549-53. doi: 10.5326/0380549. J Am Anim Hosp Assoc. 2002. PMID: 12428887
Plasma mixing studies indicated factor deficiency or dysfunction rather than factor inhibition. Feline factor XI deficiency in one adult cat has been previously reported but was attributed to factor XI inhibitors. The signal …
Plasma mixing studies indicated factor deficiency or dysfunction rather than factor inhibition. Feline factor …
The use of desmopressin in congenital factor XI deficiency: a systematic review.
Franchini M, Manzato F, Salvagno GL, Montagnana M, Lippi G. Franchini M, et al. Ann Hematol. 2009 Oct;88(10):931-5. doi: 10.1007/s00277-009-0792-9. Epub 2009 Jul 17. Ann Hematol. 2009. PMID: 19609524 Review.
Factor XI (FXI) deficiency is a rare inherited coagulation disorder characterized by infrequent spontaneous bleeding, but increased risk of hemorrhagic complications especially after trauma or surgery. ...The current knowledge on the use of the latter agent i …
Factor XI (FXI) deficiency is a rare inherited coagulation disorder characterized by infrequent spontaneous bleeding, b …
Congenital factor XI deficiency caused by a novel F11 missense variant: a case report.
Gotovac Jerčić K, Blažeković A, Hančević M, Bilić E, Borovečki F. Gotovac Jerčić K, et al. Croat Med J. 2020 Feb 29;61(1):62-65. doi: 10.3325/cmj.2020.61.62. Croat Med J. 2020. PMID: 32118380 Free PMC article.
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population but relatively common among Ashkenazi Jews. ...Homozygotes or compound heterozygotes typically show severe FXI deficiency, whereas heterozygotes show part …
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population but relatively common …
171 results