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

Year Number of Results
1953 2
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1955 1
1961 2
1962 1
1964 2
1965 2
1966 1
1967 2
1968 6
1969 3
1970 4
1971 5
1972 5
1973 4
1974 3
1975 8
1976 5
1977 4
1978 6
1979 4
1980 3
1981 11
1982 12
1983 83
1984 103
1985 136
1986 149
1987 125
1988 114
1989 130
1990 98
1991 89
1992 80
1993 94
1994 64
1995 87
1996 75
1997 65
1998 66
1999 55
2000 57
2001 59
2002 65
2003 49
2004 65
2005 60
2006 60
2007 67
2008 71
2009 81
2010 67
2011 94
2012 107
2013 108
2014 119
2015 124
2016 114
2017 105
2018 107
2019 118
2020 149
2021 168
2022 144
2023 150
2024 127
2025 14

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3,876 results

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Page 1
Acquired Hemophilia A.
Pai M. Pai M. Hematol Oncol Clin North Am. 2021 Dec;35(6):1131-1142. doi: 10.1016/j.hoc.2021.07.007. Epub 2021 Sep 15. Hematol Oncol Clin North Am. 2021. PMID: 34535289 Review.
Acquired hemophilia A is a potentially severe bleeding disorder caused by antibodies against the patient's own factor VIII. ...Treatment of acquired hemophilia A involves control of bleeding, and eradication of the inhibitor....
Acquired hemophilia A is a potentially severe bleeding disorder caused by antibodies against the patient's own factor V
Principles of care for acquired hemophilia.
Dolan G, Benson G, Bowyer A, Eichler H, Hermans C, Jiménez-Yuste V, Ljung R, Pollard D, Santagostino E, Šalek SZ. Dolan G, et al. Eur J Haematol. 2021 Jun;106(6):762-773. doi: 10.1111/ejh.13592. Epub 2021 Mar 18. Eur J Haematol. 2021. PMID: 33527471 Free PMC article. Review.
OBJECTIVE: To establish clear priorities for the care of patients with acquired hemophilia A (AHA) by proposing 10 key principles of practical, holistic AHA management. METHOD: These principles were developed by the Zurich Haemophilia Forum, an expert …
OBJECTIVE: To establish clear priorities for the care of patients with acquired hemophilia A (AHA) by proposing 10 key …
International recommendations on the diagnosis and treatment of acquired hemophilia A.
Tiede A, Collins P, Knoebl P, Teitel J, Kessler C, Shima M, Di Minno G, d'Oiron R, Salaj P, Jiménez-Yuste V, Huth-Kühne A, Giangrande P. Tiede A, et al. Haematologica. 2020 Jul;105(7):1791-1801. doi: 10.3324/haematol.2019.230771. Epub 2020 May 7. Haematologica. 2020. PMID: 32381574 Free PMC article.
Acquired hemophilia A (AHA), a rare bleeding disorder caused by neutralizing autoantibodies against coagulation factor VIII (FVIII), occurs in both men and women without a previous history of bleeding. ...
Acquired hemophilia A (AHA), a rare bleeding disorder caused by neutralizing autoantibodies against coagulation factor
Acquired hemophilia A: Updated review of evidence and treatment guidance.
Kruse-Jarres R, Kempton CL, Baudo F, Collins PW, Knoebl P, Leissinger CA, Tiede A, Kessler CM. Kruse-Jarres R, et al. Am J Hematol. 2017 Jul;92(7):695-705. doi: 10.1002/ajh.24777. Epub 2017 Jun 5. Am J Hematol. 2017. PMID: 28470674 Free article. Review.
Acquired hemophilia A (AHA) is a rare disease resulting from autoantibodies (inhibitors) against endogenous factor VIII (FVIII) that leads to bleeding, which is often spontaneous and severe. ...
Acquired hemophilia A (AHA) is a rare disease resulting from autoantibodies (inhibitors) against endogenous factor VIII
[Acquired hemophilia].
Milanesio M, Tabares AH, Caeiro GA, Olmedo J, Montivero AR. Milanesio M, et al. Rev Fac Cien Med Univ Nac Cordoba. 2022 Mar 7;79(1):57-60. doi: 10.31053/1853.0605.v79.n1.34045. Rev Fac Cien Med Univ Nac Cordoba. 2022. PMID: 35312247 Free PMC article. Spanish.
INTRODUCTION: Acquired hemophilia is a hemostasis disorder that occurs due to the presence of inhibitory autoantibodies that are directed against coagulation factor VIII. ...CONCLUSION: Acquired hemophilia is a rare disorder of hemostasis that should b …
INTRODUCTION: Acquired hemophilia is a hemostasis disorder that occurs due to the presence of inhibitory autoantibodies that a …
Acquired hemophilia A.
Webert KE. Webert KE. Semin Thromb Hemost. 2012 Oct;38(7):735-41. doi: 10.1055/s-0032-1326779. Epub 2012 Sep 1. Semin Thromb Hemost. 2012. PMID: 22941793 Review.
Acquired hemophilia A is a rare, autoimmune disorder that is caused by autoantibodies that act as inhibitors to factor VIII. ...The treatment of acquired hemophilia A has two main goals: (1) to treat and/or prevent bleeding complications
Acquired hemophilia A is a rare, autoimmune disorder that is caused by autoantibodies that act as inhibitors to factor
[Acquired hemophilia A].
Amano K. Amano K. Rinsho Ketsueki. 2018;59(6):756-763. doi: 10.11406/rinketsu.59.756. Rinsho Ketsueki. 2018. PMID: 29973457 Review. Japanese.
Successively, the disease was more readily recognized, and a revised version of the guidelines was published in December 2017. Bleeding in patients with acquired hemophilia A is typically more severe than that in patients with congenital hemophilia
Successively, the disease was more readily recognized, and a revised version of the guidelines was published in December 2017. Bleeding in p …
Diagnosis and laboratory monitoring of acquired hemophilia A.
Platton S, Sivapalaratnam S, Raheja P. Platton S, et al. Hematology Am Soc Hematol Educ Program. 2023 Dec 8;2023(1):11-18. doi: 10.1182/hematology.2023000460. Hematology Am Soc Hematol Educ Program. 2023. PMID: 38066923 Free PMC article.
Acquired hemophilia A (AHA) is a rare disorder in which autoantibodies against factor VIII (FVIII) lead to a bleeding phenotype that varies from life-threatening to no bleeding at all. ...
Acquired hemophilia A (AHA) is a rare disorder in which autoantibodies against factor VIII (FVIII) lead to a bleeding p
Treatment guidelines for acquired hemophilia A.
Windyga J, Baran B, Odnoczko E, Buczma A, Drews K, Laudanski P, Pietrzak B, Sieroszewski P. Windyga J, et al. Ginekol Pol. 2019;90(6):353-364. doi: 10.5603/GP.2019.0063. Ginekol Pol. 2019. PMID: 31276188 Free article. Review. No abstract available.
Consensus on hemophilia in Mexico.
López-Arroyo JL, Pérez-Zúñiga JM, Merino-Pasaye LE, Saavedra-González A, Alcivar-Cedeño LM, Álvarez-Vera JL, Anaya-Cuellar I, Arana-Luna LL, Ávila-Castro D, Bates-Martín RA, Cesarman-Maus G, Chávez-Aguilar LA, Peña-Celaya JA, Espitia-Ríos ME, Estrada-Domínguez P, Fermín-Caminero D, Flores-Patricio W, Chávez JG, García-Lee MT, González-Pérez MDC, González-Rubio MDC, González-Villareal MG, Ramírez-Moreno F, Hernández-Colin AK, Hernández-Ruiz E, Herrera-Olivares W, Leyto-Cruz F, Loera-Fragoso S, Martínez-Ríos A, Miranda-Madrazo MR, Morales-Hernández A, Nava-Villegas L, Orellana-Garibay JJ, Palma-Moreno OG, Paredes-Lozano EP, Peña-Alcántara P, Pérez-Lozano U, Pichardo-Cepín YM, Reynoso-Pérez AC, Rodríguez-Serna M, Rojas-Castillejos F, Romero-Rodelo H, Ruíz-Contreras JI, Segura-García A, Silva-Vera K, Soto-Cisneros PM, Tapia-Enríquez AL, Tavera-Rodríguez MG, Teomitzi-Sánchez Ó, Tepepa-Flores F, Valencia-Rivas MD, Valle-Cárdenas T, Varela-Constantino A, Javier-Morales A, Martínez-Ramírez MA, Tena-Cano S, Terrazas-Marín R, Vilchis-González SP, Villela-Peña A, Mena-Zepeda V, Ibarra MA. López-Arroyo JL, et al. Gac Med Mex. 2021;157(Suppl 1):S1-S35. doi: 10.24875/GMM.M21000463. Gac Med Mex. 2021. PMID: 33819260 Free article. English.
Hemophilia is a hemorrhagic disorder with a sex-linked inherited pattern, characterized by an inability to amplify coagulation due to a deficiency in coagulation factor VIII (hemophilia A or classic) or factor IX (hemophilia B). ...Finally, relevant re
Hemophilia is a hemorrhagic disorder with a sex-linked inherited pattern, characterized by an inability to amplify coagulation due to
3,876 results