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

Year Number of Results
1965 1
1970 1
1971 1
1975 2
1978 2
1979 1
1984 2
1987 2
1989 1
1990 1
1991 1
1992 5
1993 1
2000 2
2001 1
2003 2
2004 1
2005 1
2006 1
2007 2
2009 2
2010 5
2011 1
2012 1
2013 8
2014 2
2015 4
2016 5
2017 3
2018 1
2019 2
2020 4
2021 7
2022 5
2023 7
2024 0

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80 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.
Silent carriers of alpha thalassemia and persons with alpha or beta thalassemia trait are asymptomatic and require no treatment. Alpha thalassemia intermedia, or hemoglobin H disease, causes hemolytic anemia. Alpha thalassemia major with hemoglobin Bart's usu …
Silent carriers of alpha thalassemia and persons with alpha or beta thalassemia trait are asymptomatic and require no treatment. Alpha thala …
Non-transfusion-dependent thalassemias.
Musallam KM, Rivella S, Vichinsky E, Rachmilewitz EA. Musallam KM, et al. Haematologica. 2013 Jun;98(6):833-44. doi: 10.3324/haematol.2012.066845. Haematologica. 2013. PMID: 23729725 Free PMC article. Review.
The most commonly investigated forms are beta-thalassemia intermedia, hemoglobin E/beta-thalassemia, and alpha-thalassemia intermedia (hemoglobin H disease). However, transfusion-independence in such patients is not without side effects. ...
The most commonly investigated forms are beta-thalassemia intermedia, hemoglobin E/beta-thalassemia, and alpha-thalassemia intermedia (he …
The Clinical Phenotypes of Alpha Thalassemia.
Lal A, Vichinsky E. Lal A, et al. Hematol Oncol Clin North Am. 2023 Apr;37(2):327-339. doi: 10.1016/j.hoc.2022.12.004. Hematol Oncol Clin North Am. 2023. PMID: 36907606 Review.
Non-Transfusion-Dependent Thalassemia: A Panoramic Review.
Shash H. Shash H. Medicina (Kaunas). 2022 Oct 21;58(10):1496. doi: 10.3390/medicina58101496. Medicina (Kaunas). 2022. PMID: 36295656 Free PMC article. Review.
The most common forms of NTDT include beta-thalassemia intermedia, hemoglobin E/beta thalassemia, and hemoglobin H disease. Patients with NTDT develop several clinical complications, despite their regular transfusion independence. ...
The most common forms of NTDT include beta-thalassemia intermedia, hemoglobin E/beta thalassemia, and hemoglobin H disease …
Clinical and genetic characteristics of hemoglobin H disease in Iran.
Abolghasemi H, Kamfar S, Azarkeivan A, Karimi M, Keikhaei B, Abolghasemi F, Radfar MH, Eshghi P, Alavi S. Abolghasemi H, et al. Pediatr Hematol Oncol. 2022 Sep;39(6):489-499. doi: 10.1080/08880018.2021.2017529. Epub 2021 Dec 24. Pediatr Hematol Oncol. 2022. PMID: 34951342
Obstetric care for women with thalassemia.
Lao TT. Lao TT. Best Pract Res Clin Obstet Gynaecol. 2017 Feb;39:89-100. doi: 10.1016/j.bpobgyn.2016.09.002. Epub 2016 Sep 23. Best Pract Res Clin Obstet Gynaecol. 2017. PMID: 28341055 Review.
Although, successful pregnancy in thalassemia trait carriers and women with hemoglobin H disease is more common, there is still increased risk of obstetric and perinatal complications. ...
Although, successful pregnancy in thalassemia trait carriers and women with hemoglobin H disease is more common, there …
Clinical manifestations of α-thalassemia.
Vichinsky EP. Vichinsky EP. Cold Spring Harb Perspect Med. 2013 May 1;3(5):a011742. doi: 10.1101/cshperspect.a011742. Cold Spring Harb Perspect Med. 2013. PMID: 23543077 Free PMC article. Review.
The clinical spectrum ranges from an asymptomatic condition to a fatal in utero disease. Hemoglobin H disease results from mutations of three alpha-globin genes. ...
The clinical spectrum ranges from an asymptomatic condition to a fatal in utero disease. Hemoglobin H disease results f …
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare beta-Globin Mutations.
Qiu Y, Wei S, Hou W, Lai K, Zhu H, Li W, Li Q, Yang Z, Shu Q, Chen P, Mo W. Qiu Y, et al. Hemoglobin. 2023 Nov;47(2):52-55. doi: 10.1080/03630269.2023.2219008. Epub 2023 Jun 12. Hemoglobin. 2023. PMID: 37309066
In area where alpha-thalassemia and beta-thalassemia are prevalent, the coinheritance of hemoglobin H disease (Hb H disease) and beta-thalassemia are not uncommon and could result in complex thalassemia intermedia syndromes. ...
In area where alpha-thalassemia and beta-thalassemia are prevalent, the coinheritance of hemoglobin H disease (Hb H dis …
80 results