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

Year Number of Results
1969 1
1975 3
1976 2
1977 1
1978 1
1979 1
1980 1
1981 2
1984 1
1985 3
1986 1
1987 2
1988 1
1989 3
1993 3
1994 3
1996 1
1997 1
1998 2
1999 2
2000 1
2001 3
2002 4
2004 2
2005 2
2007 3
2008 4
2009 2
2010 2
2011 6
2012 9
2013 3
2014 5
2015 5
2016 3
2017 2
2018 2
2019 2
2020 3
2021 6
2022 6
2023 4
2024 0

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100 results

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Page 1
Hemophilia A (Factor VIII Deficiency).
Seaman CD, Xavier F, Ragni MV. Seaman CD, et al. Hematol Oncol Clin North Am. 2021 Dec;35(6):1117-1129. doi: 10.1016/j.hoc.2021.07.006. Epub 2021 Aug 10. Hematol Oncol Clin North Am. 2021. PMID: 34389199 Review.
Diagnosis of factor VIII deficiency.
Verbruggen B, Meijer P, Novákova I, Van Heerde W. Verbruggen B, et al. Haemophilia. 2008 Jul;14 Suppl 3:76-82. doi: 10.1111/j.1365-2516.2008.01715.x. Haemophilia. 2008. PMID: 18510526 Review.
The correct diagnosis of factor VIII deficiency and the assessment of severity of the disease are essential for a patient-tailored treatment strategy. ...
The correct diagnosis of factor VIII deficiency and the assessment of severity of the disease are essential for a patie …
Current challenges in the management of hemophilia.
Bauer KA. Bauer KA. Am J Manag Care. 2015 Mar;21(6 Suppl):S112-22. Am J Manag Care. 2015. PMID: 26168206 Free article. Review.
Hemophilia is characterized by genetic mutations resulting in the deficiency of factors critical to the normal process of coagulation, sometimes resulting in spontaneous bleeding into soft tissue, joints, and internal organs. The 2 most common subtypes are hemophilia A, or fac
Hemophilia is characterized by genetic mutations resulting in the deficiency of factors critical to the normal process of coagulation, somet …
Inherited bleeding disorders in older women.
Kadir RA, Sharief LA, Lee CA. Kadir RA, et al. Maturitas. 2012 May;72(1):35-41. doi: 10.1016/j.maturitas.2012.02.008. Epub 2012 Mar 22. Maturitas. 2012. PMID: 22445218 Review.
The commonest IBD is von Willebrand disease (VWD), a deficiency of von Willebrand factor (VWF), with a prevalence 1% in the general population and 13% in women with menorrhagia. Other IBDs include carriers of haemophilia A (factor VIII deficiency) and haemoph …
The commonest IBD is von Willebrand disease (VWD), a deficiency of von Willebrand factor (VWF), with a prevalence 1% in the general populati …
Gene therapy in an era of emerging treatment options for hemophilia B.
Monahan PE. Monahan PE. J Thromb Haemost. 2015 Jun;13 Suppl 1(0 1):S151-60. doi: 10.1111/jth.12957. J Thromb Haemost. 2015. PMID: 26149016 Free PMC article. Review.
Factor IX deficiency (hemophilia B) is less common than factor VIII deficiency (hemophilia A), and innovations in therapy for hemophilia B have generally lagged behind those for hemophilia A. ...
Factor IX deficiency (hemophilia B) is less common than factor VIII deficiency (hemophilia A), and innovations in thera …
Combined Factor V and VIII Deficiency with LMAN1 Mutation: A Report of 3 Saudi Siblings.
Alsheikh S, Alghamdi R, Alqatari A, Alfareed A, AlSaleh M. Alsheikh S, et al. Am J Case Rep. 2022 Sep 18;23:e937312. doi: 10.12659/AJCR.937312. Am J Case Rep. 2022. PMID: 36116005 Free PMC article.
BACKGROUND Combined factor V and factor VIII deficiency (F5F8D) is a rare bleeding disorder with an incidence of 1: 1 000 000. ...
BACKGROUND Combined factor V and factor VIII deficiency (F5F8D) is a rare bleeding disorder with an incidence of 1: 1 0 …
Autoantibodies to coagulation factors: from pathophysiology to diagnosis and therapy.
Cugno M, Gualtierotti R, Tedeschi A, Meroni PL. Cugno M, et al. Autoimmun Rev. 2014 Jan;13(1):40-8. doi: 10.1016/j.autrev.2013.08.001. Epub 2013 Aug 14. Autoimmun Rev. 2014. PMID: 23954454 Review.
The most common disorder associated with coagulation factor autoantibodies is acquired factor VIII deficiency, which is characterized by hemorrhages involving soft tissues, muscles and skin; hemarthroses are less frequent than in the inherited form. ...
The most common disorder associated with coagulation factor autoantibodies is acquired factor VIII deficiency, which is …
von Willebrand disease and pregnancy: a practical approach for the diagnosis and treatment.
Pacheco LD, Costantine MM, Saade GR, Mucowski S, Hankins GD, Sciscione AC. Pacheco LD, et al. Am J Obstet Gynecol. 2010 Sep;203(3):194-200. doi: 10.1016/j.ajog.2010.02.036. Epub 2010 Apr 24. Am J Obstet Gynecol. 2010. PMID: 20417473 Review.
Patients may have extensive mucosal bleeding (because of platelet dysfunction) and prolonged bleeding after surgery (because of factor VIII deficiency). Up to 6 different subtypes of the disease have been described, and diagnosis is based on clinical suspicio …
Patients may have extensive mucosal bleeding (because of platelet dysfunction) and prolonged bleeding after surgery (because of factor
100 results