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

Year Number of Results
1964 1
1967 2
1969 1
1970 5
1971 2
1972 1
1973 6
1974 4
1975 1
1976 4
1977 3
1978 2
1979 2
1980 5
1981 2
1982 1
1983 6
1984 1
1985 4
1986 4
1987 1
1988 4
1989 12
1990 10
1991 6
1992 5
1993 6
1994 8
1995 7
1996 6
1997 2
1998 16
1999 8
2000 8
2001 12
2002 14
2003 24
2004 16
2005 21
2006 13
2007 16
2008 15
2009 19
2010 15
2011 18
2012 11
2013 20
2014 20
2015 23
2016 19
2017 23
2018 30
2019 20
2020 23
2021 12
2022 13
2023 16
2024 8

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524 results

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Page 1
Thrombocytopenia: an update.
Smock KJ, Perkins SL. Smock KJ, et al. Int J Lab Hematol. 2014 Jun;36(3):269-78. doi: 10.1111/ijlh.12214. Int J Lab Hematol. 2014. PMID: 24750673 Review.
Investigation of the etiology of thrombocytopenia requires careful consideration of clinical history and laboratory features. ...This review article aims to summarize and address appropriate work-up of the major and/or life-threatening causes of thrombocytopenia and …
Investigation of the etiology of thrombocytopenia requires careful consideration of clinical history and laboratory features. ...This …
An update on pathogenesis and diagnosis of thrombotic thrombocytopenic purpura.
Joly BS, Coppo P, Veyradier A. Joly BS, et al. Expert Rev Hematol. 2019 Jun;12(6):383-395. doi: 10.1080/17474086.2019.1611423. Epub 2019 May 20. Expert Rev Hematol. 2019. PMID: 31107120 Review.
Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, consumption thrombocytopenia, and organ injury. TTP pathophysiology is based on a severe ADAMTS13 deficienc …
Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare and life-threatening thrombotic microangiopathy characterized by microangi …
Drug-Induced Thrombocytopenia: Mechanisms and Laboratory Diagnostics.
Danese E, Montagnana M, Favaloro EJ, Lippi G. Danese E, et al. Semin Thromb Hemost. 2020 Apr;46(3):264-274. doi: 10.1055/s-0039-1697930. Epub 2019 Sep 28. Semin Thromb Hemost. 2020. PMID: 31563127 Review.
Thrombocytopenia is a condition characterized by a decreased number of platelets in peripheral blood, which can be caused by a myriad of both congenital and acquired disorders. Drug-induced thrombocytopenia (DIT) deserves a special focus since its cumulative …
Thrombocytopenia is a condition characterized by a decreased number of platelets in peripheral blood, which can be caused by a myriad …
ADAMTS proteins in human disorders.
Mead TJ, Apte SS. Mead TJ, et al. Matrix Biol. 2018 Oct;71-72:225-239. doi: 10.1016/j.matbio.2018.06.002. Epub 2018 Jun 6. Matrix Biol. 2018. PMID: 29885460 Free PMC article. Review.
Thrombotic thrombocytopenic purpura.
Kremer Hovinga JA, Coppo P, Lämmle B, Moake JL, Miyata T, Vanhoorelbeke K. Kremer Hovinga JA, et al. Nat Rev Dis Primers. 2017 Apr 6;3:17020. doi: 10.1038/nrdp.2017.20. Nat Rev Dis Primers. 2017. PMID: 28382967 Review.
Thrombotic thrombocytopenic purpura (TTP; also known as Moschcowitz disease) is characterized by the concomitant occurrence of often severe thrombocytopenia, microangiopathic haemolytic anaemia and a variable degree of ischaemic organ damage, particularly affecting the bra …
Thrombotic thrombocytopenic purpura (TTP; also known as Moschcowitz disease) is characterized by the concomitant occurrence of often severe …
Inherited Platelet Disorders: An Updated Overview.
Palma-Barqueros V, Revilla N, Sánchez A, Zamora Cánovas A, Rodriguez-Alén A, Marín-Quílez A, González-Porras JR, Vicente V, Lozano ML, Bastida JM, Rivera J. Palma-Barqueros V, et al. Int J Mol Sci. 2021 Apr 26;22(9):4521. doi: 10.3390/ijms22094521. Int J Mol Sci. 2021. PMID: 33926054 Free PMC article. Review.
Frontiers in pathophysiology and management of thrombotic thrombocytopenic purpura.
Kubo M, Matsumoto M. Kubo M, et al. Int J Hematol. 2023 Mar;117(3):331-340. doi: 10.1007/s12185-023-03552-8. Epub 2023 Feb 9. Int J Hematol. 2023. PMID: 36757521 Review.
TTP is caused by markedly reduced ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) activity. Hereditary or congenital TTP (cTTP) is caused by ADAMTS13 gene mutations. In acquired or immune TTP (iTTP), ADAMTS13 activity is reduced …
TTP is caused by markedly reduced ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) activity. Her …
Clinical and laboratory diagnosis of TTP: an integrated approach.
Chiasakul T, Cuker A. Chiasakul T, et al. Hematology Am Soc Hematol Educ Program. 2018 Nov 30;2018(1):530-538. doi: 10.1182/asheducation-2018.1.530. Hematology Am Soc Hematol Educ Program. 2018. PMID: 30504354 Free PMC article. Review.
Thrombotic thrombocytopenia purpura (TTP) is a rare, life-threatening disease with an incidence of approximately 2 persons per million per year. ...In patients with TTP, inhibitor tests may be useful for distinguishing immune-mediated from congenital TTP. In this ar …
Thrombotic thrombocytopenia purpura (TTP) is a rare, life-threatening disease with an incidence of approximately 2 persons per millio …
Vascular tumors.
Mansfield SA, Williams RF, Iacobas I. Mansfield SA, et al. Semin Pediatr Surg. 2020 Oct;29(5):150975. doi: 10.1016/j.sempedsurg.2020.150975. Epub 2020 Sep 16. Semin Pediatr Surg. 2020. PMID: 33069294 Review.
Treatment recommendations are summarized based on the current literature. Congenital and infantile hemangiomas are covered separately in a separate chapter in this issue....
Treatment recommendations are summarized based on the current literature. Congenital and infantile hemangiomas are covered separately …
524 results