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Year Number of Results
1953 1
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1961 7
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1964 8
1965 4
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1967 4
1968 9
1969 10
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1971 10
1972 18
1973 17
1974 22
1975 12
1976 15
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1978 18
1979 14
1980 16
1981 22
1982 20
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1987 32
1988 30
1989 54
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1992 84
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1994 69
1995 71
1996 50
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1998 81
1999 65
2000 69
2001 66
2002 70
2003 71
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2005 82
2006 101
2007 90
2008 85
2009 104
2010 130
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Page 1
Showing results for thalassemia c
Search for Thalasselis C instead (2 results)
Thalassemia in Malaysia.
Alwi ZB, Syed-Hassan SR. Alwi ZB, et al. Hemoglobin. 2022 Jan;46(1):45-52. doi: 10.1080/03630269.2022.2057326. Hemoglobin. 2022. PMID: 35950577 Review.
Between 4.5 and 5.0% of the Malaysian population were reported to be carriers of this disease and 3.0-40.0% were Hb E (c.79G>A) carriers. In 2013, the Malaysian Thalassaemia Registry reported a total of 5712 registered thalassemia patients, of which 1847 h …
Between 4.5 and 5.0% of the Malaysian population were reported to be carriers of this disease and 3.0-40.0% were Hb E (c.79G>A) ca …
beta-Thalassemias.
Taher AT, Musallam KM, Cappellini MD. Taher AT, et al. N Engl J Med. 2021 Feb 25;384(8):727-743. doi: 10.1056/NEJMra2021838. N Engl J Med. 2021. PMID: 33626255 Review. No abstract available.
[Molecular genetic characteristics of a family which coinheritance of rare-88 C>G (HBB:c.-138 C>G) beta-thalassemia mutation with alpha-thalassemia and review of the literature].
Li W, Chen LT, Yu Y, Wang J, Li CY, Cai TE, Lu CJ, Li DX, Tian XJ. Li W, et al. Zhonghua Yu Fang Yi Xue Za Zhi. 2023 Feb 6;57(2):253-258. doi: 10.3760/cma.j.cn112150-20220818-00823. Zhonghua Yu Fang Yi Xue Za Zhi. 2023. PMID: 36797585 Review. Chinese.
The molecular genetic characteristics of a family with rare -88 C>G (HBB: c.-138 C>G) beta-thalassemia gene mutation were studied using cohort study. ...While her grandmother and younger brother were not carrier of thalassemia. In conclusi …
The molecular genetic characteristics of a family with rare -88 C>G (HBB: c.-138 C>G) beta-thalassemia gen …
Thalassemia in Viet Nam.
Bach KQ, Nguyen HTT, Nguyen TH, Nguyen MB, Nguyen TA. Bach KQ, et al. Hemoglobin. 2022 Jan;46(1):62-65. doi: 10.1080/03630269.2022.2069032. Hemoglobin. 2022. PMID: 35950578 Review.
The population of Viet Nam, is 96.2 million, of which 13.8% are carriers of thalassemia genes. Thalassemia/hemoglobinopathies carriers exist at different frequencies in all 54 ethnic groups of the country. ...The ethnic groups in the Northern Highland region have hi …
The population of Viet Nam, is 96.2 million, of which 13.8% are carriers of thalassemia genes. Thalassemia/hemoglobinopathies …
Thalassemia in Sri Lanka.
Premawardhena AP, Madushanka HDP. Premawardhena AP, et al. Hemoglobin. 2022 Jan;46(1):71-73. doi: 10.1080/03630269.2022.2025826. Hemoglobin. 2022. PMID: 35950586 Review.
The island nation of Sri Lanka with 22 million people (in 2020) has an estimated 2000 patients with severe thalassemia. The majority have beta-thalassemia (beta-thal) major (beta-TM), and Hb E (HBB: c.79G>A)/beta-thal accounts for most of the remainder. .. …
The island nation of Sri Lanka with 22 million people (in 2020) has an estimated 2000 patients with severe thalassemia. The majority …
Thalassemia in India.
Colah RB, Seth T. Colah RB, et al. Hemoglobin. 2022 Jan;46(1):20-26. doi: 10.1080/03630269.2021.2008958. Hemoglobin. 2022. PMID: 35950587 Review.
The GDP spent on health is one of the lowest (1.3%) resulting in high out-of-pocket expenses. The beta-thalassemias are prevalent with an estimated 7500-12000 new births each year. Hb S (HBB: c.20A>T) and Hb E (HBB: c.79G>A) are also common regionally. …
The GDP spent on health is one of the lowest (1.3%) resulting in high out-of-pocket expenses. The beta-thalassemias are prevalent wit …
Vitamin C Deficiency and Oxidant Levels in Children With Transfusion-Dependent b-Thalassemia.
Bhat KV, Sharma RA, Sharma SM, Joshi P, Dias BF, Shah N, Setia M, Manglani MV. Bhat KV, et al. Indian Pediatr. 2021 Jul 15;58(7):631-634. Epub 2021 Mar 26. Indian Pediatr. 2021. PMID: 33772531 Free article.
METHODS: This case-control study enrolled 100 children with transfusion-dependent b-thalassemia and 30 healthy controls. MDA levels before and after administration of vitamin C were performed randomly in 36 children with low vitamin C levels. ...CONCLUSIONS: …
METHODS: This case-control study enrolled 100 children with transfusion-dependent b-thalassemia and 30 healthy controls. MDA levels b …
Beta-thalassemia in Bulgaria.
Petkov GH, Efremov GD, Efremov DG, Dimovski A, Tchaicarova P, Tchaicarov R, Rogina B, Agarwal S, Kutlar A, Kutlar F, et al. Petkov GH, et al. Hemoglobin. 1990;14(1):25-33. doi: 10.3109/03630269009002252. Hemoglobin. 1990. PMID: 2200762 Review.
Analyses of DNA from 64 patients with thalassemia major using the hybridization technique of amplified DNA with radiolabeled synthetic oligonucleotide probes identified 13 different beta-thalassemia mutations. ...Promoter mutations were rare and the frequencies of t …
Analyses of DNA from 64 patients with thalassemia major using the hybridization technique of amplified DNA with radiolabeled syntheti …
Beta-thalassemia in Yugoslavia.
Dimovski A, Efremov DG, Jankovic L, Juricic D, Zisovski N, Stojanovski N, Nikolov N, Petkov GT, Reese AL, Stoming TA, et al. Dimovski A, et al. Hemoglobin. 1990;14(1):15-24. doi: 10.3109/03630269009002251. Hemoglobin. 1990. PMID: 2200761 Review.
This study concerned the evaluation of beta-thalassemia alleles in nearly 50 patients with beta-thalassemia major and in 130 -thalassemia heterozygotes using gene amplification and dot-blot hybridization with synthetic probes. ...The poly A mutation with clas …
This study concerned the evaluation of beta-thalassemia alleles in nearly 50 patients with beta-thalassemia major and in 130 - …
Thalassemia.
Cohen AR, Galanello R, Pennell DJ, Cunningham MJ, Vichinsky E. Cohen AR, et al. Hematology Am Soc Hematol Educ Program. 2004:14-34. doi: 10.1182/asheducation-2004.1.14. Hematology Am Soc Hematol Educ Program. 2004. PMID: 15561674 Review.
Thrombosis is recognized with increasing frequency as a significant complication of thalassemia major and thalassemia intermedia, and pulmonary hypertension is now the focus of intense study. ...The use of intrauterine transfusions to sustain the viability of fetuse …
Thrombosis is recognized with increasing frequency as a significant complication of thalassemia major and thalassemia intermed …
4,365 results