Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1970 1
1971 2
1974 2
1976 2
1979 4
1980 5
1981 3
1982 5
1983 7
1984 6
1985 10
1986 3
1987 9
1988 7
1989 15
1990 21
1991 17
1992 20
1993 23
1994 17
1995 26
1996 28
1997 27
1998 46
1999 22
2000 30
2001 40
2002 24
2003 33
2004 22
2005 41
2006 16
2007 31
2008 55
2009 39
2010 46
2011 47
2012 52
2013 49
2014 51
2015 50
2016 85
2017 66
2018 68
2019 52
2020 51
2021 77
2022 56
2023 62
2024 10

Text availability

Article attribute

Article type

Publication date

Search Results

1,360 results

Results by year

Filters applied: . Clear all
Page 1
Current status of beta-thalassemia and its treatment strategies.
Ali S, Mumtaz S, Shakir HA, Khan M, Tahir HM, Mumtaz S, Mughal TA, Hassan A, Kazmi SAR, Sadia, Irfan M, Khan MA. Ali S, et al. Mol Genet Genomic Med. 2021 Dec;9(12):e1788. doi: 10.1002/mgg3.1788. Epub 2021 Nov 5. Mol Genet Genomic Med. 2021. PMID: 34738740 Free PMC article. Review.
Beta-thalassemia is caused by one or more mutations in the beta-globin gene. ...METHODS: Beta-thalassemia has been further divided into three main forms: thalassemia major, intermedia, and minor/silent carrier. ...
Beta-thalassemia is caused by one or more mutations in the beta-globin gene. ...METHODS: Beta-thalassemia
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.
Beta thalassemia major causes hemolytic anemia, poor growth, and skeletal abnormalities during infancy. Affected children will require regular lifelong blood transfusions. Beta thalassemia intermedia is less severe than beta thalassemia m
Beta thalassemia major causes hemolytic anemia, poor growth, and skeletal abnormalities during infancy. Affected children will
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.
beta-Thalassemia is caused by reduced (beta(+)) or absent (beta(0)) synthesis of the beta-globin chains of hemoglobin. Three clinical and hematological conditions of increasing severity are recognized: the beta-thalassemia carrier
beta-Thalassemia is caused by reduced (beta(+)) or absent (beta(0)) synthesis of the beta-globin chains o
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
Gene Therapy for Hemoglobinopathies: Beta-Thalassemia, Sickle Cell Disease.
Leonard A, Tisdale JF, Bonner M. Leonard A, et al. Hematol Oncol Clin North Am. 2022 Aug;36(4):769-795. doi: 10.1016/j.hoc.2022.03.008. Epub 2022 Jun 27. Hematol Oncol Clin North Am. 2022. PMID: 35773052 Review.
beta-thalassemia and sickle cell disease (SCD) are the most common monogenic diseases in the world and are potentially curable after allogeneic hematopoietic stem cell transplantation (HSCT) or autologous HSCT after genetic modification. ...
beta-thalassemia and sickle cell disease (SCD) are the most common monogenic diseases in the world and are potentially curable
Hematopoietic Stem Cell Gene-Addition/Editing Therapy in Sickle Cell Disease.
Germino-Watnick P, Hinds M, Le A, Chu R, Liu X, Uchida N. Germino-Watnick P, et al. Cells. 2022 Jun 4;11(11):1843. doi: 10.3390/cells11111843. Cells. 2022. PMID: 35681538 Free PMC article. Review.
Autologous hematopoietic stem cell (HSC)-targeted gene therapy provides a one-time cure for various genetic diseases including sickle cell disease (SCD) and beta-thalassemia. SCD is caused by a point mutation (20A > T) in the beta-globin gene. Since SCD is …
Autologous hematopoietic stem cell (HSC)-targeted gene therapy provides a one-time cure for various genetic diseases including sickle cell d …
Changing patterns in the epidemiology of beta-thalassemia.
Kattamis A, Forni GL, Aydinok Y, Viprakasit V. Kattamis A, et al. Eur J Haematol. 2020 Dec;105(6):692-703. doi: 10.1111/ejh.13512. Epub 2020 Sep 21. Eur J Haematol. 2020. PMID: 32886826 Free PMC article. Review.
Traditionally, beta-thalassemia has been more common in certain regions of the world such as the Mediterranean, Middle East, and Southeast Asia. However, the prevalence of beta-thalassemia is increasing in other regions, including Northern Europe and N …
Traditionally, beta-thalassemia has been more common in certain regions of the world such as the Mediterranean, Middle East, a …
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 …
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.
Beta-thalassemia is caused by the reduced (beta) or absent (beta) synthesis of the beta globin chains of the hemoglobin tetramer. ...The beta-thalassemia carrier state, which results from heterozygosity for beta-thalassem
Beta-thalassemia is caused by the reduced (beta) or absent (beta) synthesis of the beta globin chains of
Beta-thalassemia.
Galanello R, Origa R. Galanello R, et al. Orphanet J Rare Dis. 2010 May 21;5:11. doi: 10.1186/1750-1172-5-11. Orphanet J Rare Dis. 2010. PMID: 20492708 Free PMC article. Review.
Beta-thalassemias are caused by point mutations or, more rarely, deletions in the beta globin gene on chromosome 11, leading to reduced (beta+) or absent (beta0) synthesis of the beta chains of hemoglobin (Hb). ...Prognosis for individuals with beta
Beta-thalassemias are caused by point mutations or, more rarely, deletions in the beta globin gene on chromosome 11, leading t
1,360 results