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

Year Number of Results
1960 1
1961 1
1962 1
1963 1
1964 3
1965 6
1966 1
1967 2
1968 12
1969 16
1970 14
1971 17
1972 26
1973 20
1974 13
1975 11
1976 11
1977 13
1978 14
1979 9
1980 25
1981 12
1982 11
1983 13
1984 11
1985 14
1986 10
1987 12
1988 10
1989 16
1990 9
1991 16
1992 10
1993 13
1994 6
1995 12
1996 19
1997 12
1998 15
1999 16
2000 17
2001 13
2002 13
2003 20
2004 20
2005 19
2006 24
2007 19
2008 31
2009 27
2010 33
2011 36
2012 39
2013 54
2014 48
2015 48
2016 51
2017 46
2018 37
2019 38
2020 44
2021 43
2022 41
2023 54
2024 21

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1,179 results

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Page 1
Factor XIII Deficiency.
Karimi M, Bereczky Z, Cohan N, Muszbek L. Karimi M, et al. Semin Thromb Hemost. 2009 Jun;35(4):426-38. doi: 10.1055/s-0029-1225765. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598071 Review.
Factor XIII (FXIII) is a tetrameric zymogen (FXIII-A (2)B (2)) that is converted into an active transglutaminase (FXIIIa) by thrombin and Ca (2+) in the terminal phase of the clotting cascade. ...In addition, impaired wound healing and spontaneous abortion in women
Factor XIII (FXIII) is a tetrameric zymogen (FXIII-A (2)B (2)) that is converted into an active transglutaminase (FXIIIa) by t
Acquired factor XIII deficiency: A review.
Yan MTS, Rydz N, Goodyear D, Sholzberg M. Yan MTS, et al. Transfus Apher Sci. 2018 Dec;57(6):724-730. doi: 10.1016/j.transci.2018.10.013. Epub 2018 Oct 30. Transfus Apher Sci. 2018. PMID: 30446212 Review.
Acquired factor XIII (FXIII) deficiency is a rare bleeding disorder that can manifest with spontaneous or delayed life-threatening hemorrhage. ...Cases are described to illustrate the clinical features of acquired FXIII deficiency....
Acquired factor XIII (FXIII) deficiency is a rare bleeding disorder that can manifest with spontaneous or delayed life- …
Factor XIII deficiency diagnosis: Challenges and tools.
Karimi M, Peyvandi F, Naderi M, Shapiro A. Karimi M, et al. Int J Lab Hematol. 2018 Feb;40(1):3-11. doi: 10.1111/ijlh.12756. Epub 2017 Oct 13. Int J Lab Hematol. 2018. PMID: 29027765 Free article. Review.
Factor XIII deficiency (FXIIID) is a rare hereditary bleeding disorder arising from heterogeneous mutations, which can lead to life-threatening hemorrhage. ...
Factor XIII deficiency (FXIIID) is a rare hereditary bleeding disorder arising from heterogeneous mutations, which can
Factor XIII Deficiency: A Review of Clinical Presentation and Management.
Pelcovits A, Schiffman F, Niroula R. Pelcovits A, et al. Hematol Oncol Clin North Am. 2021 Dec;35(6):1171-1180. doi: 10.1016/j.hoc.2021.07.009. Epub 2021 Oct 2. Hematol Oncol Clin North Am. 2021. PMID: 34607717 Review.
Factor XIII (FXIII) deficiency is a rare autosomal recessive disorder that can result in life-threatening bleeding and early fetal loss. ...
Factor XIII (FXIII) deficiency is a rare autosomal recessive disorder that can result in life-threatening bleeding and
Factor XIII deficiency management: a review of the literature.
Odame JE, Chan AK, Wu JK, Breakey VR. Odame JE, et al. Blood Coagul Fibrinolysis. 2014 Apr;25(3):199-205. doi: 10.1097/MBC.0000000000000029. Blood Coagul Fibrinolysis. 2014. PMID: 24401950 Review.
Factor XIII (FXIII) deficiency is a rare congenital bleeding disorder estimated to affect 1 in 2 million live births. ...Common bleeding manifestations included umbilical cord bleeding, ICH and hematomas. Patients were generally placed on prophylactic fact
Factor XIII (FXIII) deficiency is a rare congenital bleeding disorder estimated to affect 1 in 2 million live births. .
Factor XIII deficiency.
Anwar R, Miloszewski KJ. Anwar R, et al. Br J Haematol. 1999 Dec;107(3):468-84. doi: 10.1046/j.1365-2141.1999.01648.x. Br J Haematol. 1999. PMID: 10583246 Free article. Review. No abstract available.
Factor XIII deficiency: an update.
Schroeder V, Kohler HP. Schroeder V, et al. Semin Thromb Hemost. 2013 Sep;39(6):632-41. doi: 10.1055/s-0033-1353392. Epub 2013 Aug 8. Semin Thromb Hemost. 2013. PMID: 23929307 Review.
Confirmation of suspected congenital factor XIII (FXIII) deficiency still represents a diagnostic challenge in the field of rare bleeding disorders. ...This review gives a detailed overview and update about congenital FXIII deficiency, its epidemiology …
Confirmation of suspected congenital factor XIII (FXIII) deficiency still represents a diagnostic challenge in the fiel …
Diagnosis of factor XIII deficiency.
Dorgalaleh A, Tabibian S, Hosseini MS, Farshi Y, Roshanzamir F, Naderi M, Kazemi A, Zaker F, Aghideh AN, Shamsizadeh M. Dorgalaleh A, et al. Hematology. 2016 Aug;21(7):430-9. doi: 10.1080/10245332.2015.1101975. Epub 2016 Mar 30. Hematology. 2016. PMID: 27077776 Review.
BACKGROUND: Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with estimated incidence of one per two million. All routine coagulation tests are normal in FXIII deficiency (FXIIID), which complicates the diagnosis of this disorder. …
BACKGROUND: Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with estimated incidence of one per t …
The impact of acquired coagulation factor XIII deficiency in traumatic bleeding and wound healing.
Kleber C, Sablotzki A, Casu S, Olivieri M, Thoms KM, Horter J, Schmitt FCF, Birschmann I, Fries D, Maegele M, Schöchl H, Wilhelmi M. Kleber C, et al. Crit Care. 2022 Mar 24;26(1):69. doi: 10.1186/s13054-022-03940-2. Crit Care. 2022. PMID: 35331308 Free PMC article. Review.
Factor XIII (FXIII) is a protein involved in blood clot stabilisation which also plays an important role in processes including trauma, wound healing, tissue repair, pregnancy, and even bone metabolism. ...This narrative review discusses altered FXIII levels in trau
Factor XIII (FXIII) is a protein involved in blood clot stabilisation which also plays an important role in processes includin
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.
Biswas A, Ivaskevicius V, Thomas A, Oldenburg J. Biswas A, et al. Hamostaseologie. 2014;34(2):160-6. doi: 10.5482/HAMO-13-08-0046. Epub 2014 Feb 7. Hamostaseologie. 2014. PMID: 24503678 Review.
The zymogenic plasma FXIII molecule is a heterotetramer composed of two catalytic FXIII-A and two protective FXIII-B subunits. Factor XIII deficiency resulting from inherited or acquired causes can result in pathological bleeding episodes. ...Here, we update …
The zymogenic plasma FXIII molecule is a heterotetramer composed of two catalytic FXIII-A and two protective FXIII-B subunits. Factor
1,179 results