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Volumn 32, Issue 1, 2010, Pages 76-78

The frequency of β-globin gene haplotypes, α-thalassemia and genetic polymorphisms of methylenetetrahydrofolate reductase, factor V leiden and prothrombin genes in children with sickle cell disease in Rio de Janeiro, Brazil;Frequência dos haplótipos da globina beta, da talassemia alfa e dos polimorfismos genéticos dos genes da metilenotetrahidrofolato redutase, do fator v leiden e da protrombina em crianças com doença falciforme no rio de Janeiro, Brasil

Author keywords

Blood coagulation; Factor V leiden; Hemoglobinopathies; Prothrombin; Sickle cell disease; Thalassemia

Indexed keywords


EID: 77952760286     PISSN: 15168484     EISSN: None     Source Type: Journal    
DOI: 10.1590/s1516-84842010000100017     Document Type: Letter
Times cited : (6)

References (7)
  • 1
    • 34249020755 scopus 로고    scopus 로고
    • Niger-Congo speaking populations and the formation of the Brazilian gene pool: Mt DNA and Y-chromosome data
    • Hünemeier T, Carvalho C, Marrero RA, Salzano FM, Junho Pena SD, Bortolini MC. Niger-Congo speaking populations and the formation of the Brazilian gene pool: mt DNA and Y-chromosome data. Am J Phys Anthropol. 2007; 133(2):854-67.
    • (2007) Am J Phys Anthropol , vol.133 , Issue.2 , pp. 854-867
    • Hünemeier, T.1    Carvalho, C.2    Marrero, R.A.3    Salzano, F.M.4    Junho, P.S.D.5    Bortolini, M.C.6
  • 3
    • 0025776006 scopus 로고
    • High prevalence of -thalassemia in a black population of Brazil
    • Sonati MF, Costa, FF, Botura C. High prevalence of -thalassemia in a black population of Brazil. Hemoglobin. 1991; 15:309-11.
    • (1991) Hemoglobin , vol.15 , pp. 309-311
    • Sonati, M.F.1    Costa, F.F.2    Botura, C.3
  • 5
    • 0031825212 scopus 로고    scopus 로고
    • Prothrombin mutant, Factor v Leiden and thermolabile variant ofmethylenetetrahydrofolate reductase amog patients with sickle cell disease in Brazil
    • Andrade FL, Annichino-Bizzacchi AJM, Saad ST, Costa FF, Arruda VR. Prothrombin mutant, Factor v Leiden and thermolabile variant ofmethylenetetrahydrofolate reductase amog patients with sickle cell disease in Brazil. Am J Hematol.1998;59:46-50.
    • (1998) Am J Hematol , vol.59 , pp. 46-50
    • Andrade, F.L.1    Annichino-Bizzacchi, A.J.M.2    Saad, S.T.3    Costa, F.F.4    Arruda, V.R.5
  • 6
    • 33847643697 scopus 로고    scopus 로고
    • Noguiti MAE, et al.The clinical impacto of MTHFR polymorphisms on the vascular complications of sickle cell disease
    • Neto FM, Lourenço DM, Noguiti MAE, et al.The clinical impacto of MTHFR polymorphisms on the vascular complications of sickle cell disease. Braz Med Biol Res. 2006;39(10):1291-5.
    • (2006) Braz Med Biol Res , vol.39 , Issue.10 , pp. 1291-1295
    • Neto, F.M.1    Lourenço, D.M.2
  • 7
    • 4544305476 scopus 로고    scopus 로고
    • AC677T methylenetetrahydrofolate reductase (MTHFR) polymorphisms and G20210A mutation in the prothrombin gene of sickle cell anemia patients from Northeast Brazil
    • Couto FD, Vilas Boas W, Lyra I, Zanette A, Dupuit MF, Almeida MN, et al. AC677T methylenetetrahydrofolate reductase (MTHFR) polymorphisms and G20210A mutation in the prothrombin gene of sickle cell anemia patients from Northeast Brazil. Hemoglobin. 2004;28(3):237-41.
    • (2004) Hemoglobin , vol.28 , Issue.3 , pp. 237-241
    • Couto, F.D.1    Vilas, B.W.2    Lyra, I.3    Zanette, A.4    Dupuit, M.F.5    Almeida, M.N.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.