Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1968
2025

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

Year Number of Results
1968 2
1969 1
1970 1
1974 2
1975 1
1976 4
1977 1
1978 1
1979 1
1980 5
1982 3
1983 3
1984 2
1985 9
1986 1
1987 2
1988 2
1989 11
1990 8
1991 5
1992 5
1993 9
1994 12
1995 7
1996 20
1997 13
1998 14
1999 12
2000 17
2001 22
2002 22
2003 14
2004 21
2005 31
2006 17
2007 23
2008 12
2009 16
2010 15
2011 13
2012 18
2013 20
2014 15
2015 20
2016 24
2017 21
2018 16
2019 17
2020 16
2021 15
2022 14
2023 23
2024 18
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

566 results

Results by year

Filters applied: . Clear all
Page 1
Syndromes of thrombotic microangiopathy.
George JN, Nester CM. George JN, et al. N Engl J Med. 2014 Aug 14;371(7):654-66. doi: 10.1056/NEJMra1312353. N Engl J Med. 2014. PMID: 25119611 Free article. Review.
This review article covers the diverse pathophysiological pathways that can lead to microangiopathic hemolytic anemia and a procoagulant state with or without damage to the kidneys and other organs....
This review article covers the diverse pathophysiological pathways that can lead to microangiopathic hemolytic anemia and a pr …
The diagnostic protocol for hereditary spherocytosis-2021 update.
Wu Y, Liao L, Lin F. Wu Y, et al. J Clin Lab Anal. 2021 Dec;35(12):e24034. doi: 10.1002/jcla.24034. Epub 2021 Oct 24. J Clin Lab Anal. 2021. PMID: 34689357 Free PMC article. Review.
The objective of this study was to propose a simple and practical diagnostic protocol, which can contribute to the diagnosis of HS and its differential diagnosis with different types of hemolytic anemia such as thalassemia (THAL), autoimmune hemolytic anem
The objective of this study was to propose a simple and practical diagnostic protocol, which can contribute to the diagnosis of HS and its d …
Understanding Sickle cell disease: Causes, symptoms, and treatment options.
Elendu C, Amaechi DC, Alakwe-Ojimba CE, Elendu TC, Elendu RC, Ayabazu CP, Aina TO, Aborisade O, Adenikinju JS. Elendu C, et al. Medicine (Baltimore). 2023 Sep 22;102(38):e35237. doi: 10.1097/MD.0000000000035237. Medicine (Baltimore). 2023. PMID: 37746969 Free PMC article. Review.
Patients with SCD may experience recurrent pain, fatigue, anemia, and increased infection susceptibility. Treatment options for SCD focus on managing symptoms and preventing complications. ...Finally, understanding the causes, symptoms, and treatment options for SCD is cru …
Patients with SCD may experience recurrent pain, fatigue, anemia, and increased infection susceptibility. Treatment options for SCD f …
Hemolytic anemia.
Dhaliwal G, Cornett PA, Tierney LM Jr. Dhaliwal G, et al. Am Fam Physician. 2004 Jun 1;69(11):2599-606. Am Fam Physician. 2004. PMID: 15202694 Free article. Review.
The etiologies of hemolysis often are categorized as acquired or hereditary. Common acquired causes of hemolytic anemia are autoimmunity, microangiopathy, and infection. Immune-mediated hemolysis, caused by antierythrocyte antibodies, can be secondary to malignancie …
The etiologies of hemolysis often are categorized as acquired or hereditary. Common acquired causes of hemolytic anemia are au …
Beta-thalassemia.
Cao A, Galanello R. Cao A, et al. Genet Med. 2010 Feb;12(2):61-76. doi: 10.1097/GIM.0b013e3181cd68ed. Genet Med. 2010. PMID: 20098328 Free article. Review.
Thalassemia major is a severe transfusion-dependent anemia. Thalassemia intermedia comprehend a clinically and genotypically very heterogeneous group of thalassemia-like disorders, ranging in severity from the asymptomatic carrier state to the severe transfusion-dependent …
Thalassemia major is a severe transfusion-dependent anemia. Thalassemia intermedia comprehend a clinically and genotypically very het …
Thrombotic microangiopathies of pregnancy: Differential diagnosis.
Gupta M, Feinberg BB, Burwick RM. Gupta M, et al. Pregnancy Hypertens. 2018 Apr;12:29-34. doi: 10.1016/j.preghy.2018.02.007. Epub 2018 Feb 16. Pregnancy Hypertens. 2018. PMID: 29674195 Review.
Thrombotic microangiopathy (TMA) disorders are characterized by microangiopathic hemolytic anemia, thrombocytopenia and end-organ injury. In pregnancy and postpartum, TMA is most commonly encountered with HELLP (hemolysis, elevated liver enzymes, low platelet count …
Thrombotic microangiopathy (TMA) disorders are characterized by microangiopathic hemolytic anemia, thrombocytopenia and end-or …
Thalassaemia in China.
Wang WD, Hu F, Zhou DH, Gale RP, Lai YR, Yao HX, Li C, Wu BY, Chen Z, Fang JP, Chen SJ, Liang Y. Wang WD, et al. Blood Rev. 2023 Jul;60:101074. doi: 10.1016/j.blre.2023.101074. Epub 2023 Mar 17. Blood Rev. 2023. PMID: 36963988 Review.
For example, regional differences in access to medical care and unequal economic development require innovations to reduce the medical, financial and psychological burdens of Chinese with thalassaemia and their families. In this review we discuss success in preventing and …
For example, regional differences in access to medical care and unequal economic development require innovations to reduce the medical, fina …
Plasma cell neoplasms and related entities-evolution in diagnosis and classification.
Fend F, Dogan A, Cook JR. Fend F, et al. Virchows Arch. 2023 Jan;482(1):163-177. doi: 10.1007/s00428-022-03431-3. Epub 2022 Nov 21. Virchows Arch. 2023. PMID: 36414803 Free PMC article. Review.
MM with recurrent genetic abnormalities includes MM with CCND family translocations, MM with MAF family translocations, MM with NSD2 translocation, and MM with hyperdiploidy, with the remaining cases classified as MM, NOS. ...
MM with recurrent genetic abnormalities includes MM with CCND family translocations, MM with MAF family translocations, MM wit …
Human parvovirus B19.
Heegaard ED, Brown KE. Heegaard ED, et al. Clin Microbiol Rev. 2002 Jul;15(3):485-505. doi: 10.1128/CMR.15.3.485-505.2002. Clin Microbiol Rev. 2002. PMID: 12097253 Free PMC article. Review.
Due to the tropism of B19 to erythroid progenitor cells, infection in individuals with an underlying hemolytic disorder causes transient aplastic crisis. In the immunocompromised host persistent B19 infection is manifested as pure red cell aplasia and chronic anemia
Due to the tropism of B19 to erythroid progenitor cells, infection in individuals with an underlying hemolytic disorder causes transi …
The hemoglobinopathies, molecular disease mechanisms and diagnostics.
Harteveld CL, Achour A, Arkesteijn SJG, Ter Huurne J, Verschuren M, Bhagwandien-Bisoen S, Schaap R, Vijfhuizen L, El Idrissi H, Koopmann TT. Harteveld CL, et al. Int J Lab Hematol. 2022 Sep;44 Suppl 1(Suppl 1):28-36. doi: 10.1111/ijlh.13885. Int J Lab Hematol. 2022. PMID: 36074711 Free PMC article. Review.
The disease mechanisms may involve duplicated alpha-globin genes, mosaic partial Uniparental Isodisomy of chromosome 11p15.4 where the HBB gene is located or haplo-insufficiency of a non-linked gene SUPT5H on chromosome 19q, first described in two Dutch families with beta- …
The disease mechanisms may involve duplicated alpha-globin genes, mosaic partial Uniparental Isodisomy of chromosome 11p15.4 where the HBB g …
566 results