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

Year Number of Results
1970 1
1973 1
1974 3
1975 3
1976 1
1978 1
1979 2
1980 3
1981 3
1982 2
1983 3
1984 2
1985 4
1986 4
1987 4
1988 8
1989 24
1990 25
1991 21
1992 19
1993 17
1994 12
1995 23
1996 17
1997 26
1998 26
1999 18
2000 19
2001 17
2002 10
2003 30
2004 23
2005 31
2006 20
2007 19
2008 28
2009 26
2010 28
2011 17
2012 28
2013 31
2014 24
2015 34
2016 37
2017 42
2018 30
2019 24
2020 22
2021 29
2022 38
2023 33
2024 14

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857 results

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Page 1
Alpha and beta thalassemia.
Muncie HL Jr, Campbell J. Muncie HL Jr, et al. Am Fam Physician. 2009 Aug 15;80(4):339-44. Am Fam Physician. 2009. PMID: 19678601 Free article. Review.
Alpha thalassemia intermedia, or hemoglobin H disease, causes hemolytic anemia. Alpha thalassemia major with hemoglobin Bart's usually results in fatal hydrops fetalis. ...
Alpha thalassemia intermedia, or hemoglobin H disease, causes hemolytic anemia. Alpha thalassemia major with hem
Clinical Classification, Screening and Diagnosis for Thalassemia.
Viprakasit V, Ekwattanakit S. Viprakasit V, et al. Hematol Oncol Clin North Am. 2018 Apr;32(2):193-211. doi: 10.1016/j.hoc.2017.11.006. Hematol Oncol Clin North Am. 2018. PMID: 29458726 Review.
At present, thalassemia diseases are classified into transfusion-dependent thalassemia and non-transfusion-dependent thalassemia. This classification is based on the clinical severity of patients determining whether they do require regular blood transfusions …
At present, thalassemia diseases are classified into transfusion-dependent thalassemia and non-transfusion-dependent thalas
beta-Thalassemia.
Origa R. Origa R. Genet Med. 2017 Jun;19(6):609-619. doi: 10.1038/gim.2016.173. Epub 2016 Nov 3. Genet Med. 2017. PMID: 27811859 Free article. Review.
Three clinical and hematological conditions of increasing severity are recognized: the beta-thalassemia carrier state, thalassemia intermedia, and thalassemia major, a severe transfusion-dependent anemia. ...Factors include the inheritance of mild/silent beta …
Three clinical and hematological conditions of increasing severity are recognized: the beta-thalassemia carrier state, thalassemia
Thalassemia in Indonesia.
Wahidiyat PA, Sari TT, Rahmartani LD, Iskandar SD, Pratanata AM, Yapiy I, Setianingsih I, Atmakusuma TD, Lubis AM. Wahidiyat PA, et al. Hemoglobin. 2022 Jan;46(1):39-44. doi: 10.1080/03630269.2021.2023565. Hemoglobin. 2022. PMID: 35950580 Review.
Indonesia is located along the 'Thalassemia Belt' and a hotspot for hemoglobinopathies. Around 3.0-10.0% of the population carry beta-thalassemia (beta-thal) and 2.6-11.0% of the population carry alpha-thalassemia (alpha-thal). ...In line with t …
Indonesia is located along the 'Thalassemia Belt' and a hotspot for hemoglobinopathies. Around 3.0-10.0% of the population carry beta …
Molecular basis of alpha-thalassemia.
Farashi S, Harteveld CL. Farashi S, et al. Blood Cells Mol Dis. 2018 May;70:43-53. doi: 10.1016/j.bcmd.2017.09.004. Epub 2017 Sep 21. Blood Cells Mol Dis. 2018. PMID: 29032940 Free article. Review.
alpha-Thalassemia is an inherited, autosomal recessive, disorder characterized by a microcytic hypochromic anemia. ...Deletions and point mutations in the alpha-globin genes and their regulatory elements have been studied extensively in carriers and patients
alpha-Thalassemia is an inherited, autosomal recessive, disorder characterized by a microcytic hypochromic anemia. ...Deletion
The alpha-thalassemias.
Piel FB, Weatherall DJ. Piel FB, et al. N Engl J Med. 2014 Nov 13;371(20):1908-16. doi: 10.1056/NEJMra1404415. N Engl J Med. 2014. PMID: 25390741 Free article. Review.
More than 100 varieties of alpha-thalassemia have been identified. Their geographic distribution and the challenges associated with screening, diagnosis, and management suggest that alpha-thalassemias should have a higher priority on global public health agen …
More than 100 varieties of alpha-thalassemia have been identified. Their geographic distribution and the challenges associated …
Laboratory diagnosis of thalassemia.
Brancaleoni V, Di Pierro E, Motta I, Cappellini MD. Brancaleoni V, et al. Int J Lab Hematol. 2016 May;38 Suppl 1:32-40. doi: 10.1111/ijlh.12527. Epub 2016 May 16. Int J Lab Hematol. 2016. PMID: 27183541 Review.
HbA2 determination is the most decisive test for beta-carrier detection although it can be disturbed by the presence of delta-thalassemia defects. In alpha-thalassemia, HbA2 can be lower than normal and it assumes significant value when iron deficiency is exc …
HbA2 determination is the most decisive test for beta-carrier detection although it can be disturbed by the presence of delta-thalassemia
Alpha-thalassaemia.
Harteveld CL, Higgs DR. Harteveld CL, et al. Orphanet J Rare Dis. 2010 May 28;5:13. doi: 10.1186/1750-1172-5-13. Orphanet J Rare Dis. 2010. PMID: 20507641 Free PMC article. Review.
Alpha thalassaemia most frequently results from deletion of one or both alpha genes from the chromosome and can be classified according to its genotype/phenotype correlation. ...Molecular analysis is usually required to confirm the haematological observations
Alpha thalassaemia most frequently results from deletion of one or both alpha genes from the chromosome and can be clas
Prevalence and Management of beta-Thalassemia in India.
Yadav SS, Panchal P, Menon KC. Yadav SS, et al. Hemoglobin. 2022 Jan;46(1):27-32. doi: 10.1080/03630269.2021.2001346. Epub 2022 Feb 7. Hemoglobin. 2022. PMID: 35129043 Review.
India bears a huge burden of hemoglobinopathies, and the most prevalent is thalassemia. The different types of thalassemia include minor, major and intermedia, based on the alpha/beta-globin chain inequality. This review aimed to understand the current preval …
India bears a huge burden of hemoglobinopathies, and the most prevalent is thalassemia. The different types of thalassemia inc …
Sickle Cell Disease.
Piel FB, Steinberg MH, Rees DC. Piel FB, et al. N Engl J Med. 2017 Apr 20;376(16):1561-1573. doi: 10.1056/NEJMra1510865. N Engl J Med. 2017. PMID: 28423290 Free article. Review. No abstract available.
857 results