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
|
-
1
-
-
34249020755
-
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
-
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
-
4
-
-
55349132333
-
Clinical and molecular characteristics of sickle cell anemia in the northeast of Brazil
-
Adorno EV, Zanette A, Lyra I, Seixas MO, Reis MG, Gonçalves MS. Clinical and molecular characteristics of sickle cell anemia in the northeast of Brazil. Genetics and Mol Biol. 2008; 31(3):621-5.
-
(2008)
Genetics and Mol Biol
, vol.31
, Issue.3
, pp. 621-625
-
-
Adorno, E.V.1
Zanette, A.2
Lyra, I.3
Seixas, M.O.4
Reis, M.G.5
Gonçalves, M.S.6
-
5
-
-
0031825212
-
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
-
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
-
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
|