Gonçalves MS - Search Results

1

Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil.

Gonçalves MS, Fahel S, Figueiredo MS, Kimura EJ, Nechtman F, Stoming TA, Arruda VR, Saad ST, Costa FF. Gonçalves MS, et al. Ann Hematol. 1995 Mar;70(3):159-61. doi: 10.1007/BF01682037. Ann Hematol. 1995. PMID: 7536477

2

Effect of alpha-thalassemia and beta-globin gene cluster haplotypes on the hematological and clinical features of sickle-cell anemia in Brazil.

Figueiredo MS, Kerbauy J, Gonçalves MS, Arruda VR, Saad ST, Sonati MF, Stoming T, Costa FF. Figueiredo MS, et al. Among authors: goncalves ms. Am J Hematol. 1996 Oct;53(2):72-6. doi: 10.1002/(SICI)1096-8652(199610)53:2<72::AID-AJH3>3.0.CO;2-0. Am J Hematol. 1996. PMID: 8892730 Free article.

3

Haplotype analysis and Agamma gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin.

Bordin S, Martins JT, Gonçalves MS, Melo MB, Saad ST, Costa FF. Bordin S, et al. Among authors: goncalves ms. Am J Hematol. 1998 May;58(1):49-54. doi: 10.1002/(sici)1096-8652(199805)58:1<49::aid-ajh9>3.0.co;2-0. Am J Hematol. 1998. PMID: 9590149 Free article.

4

Sickle cell disease in a Brazilian population from Sao Paulo: a study of the beta s haplotypes.

Goncalves MS, Nechtman JF, Figueiredo MS, Kerbauy J, Arruda VR, Sonati MF, Saad SO, Costa FF, Stoming TA. Goncalves MS, et al. Hum Hered. 1994 Nov-Dec;44(6):322-7. doi: 10.1159/000154238. Hum Hered. 1994. PMID: 7860085

5

Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?

Arruda VR, Grignolli CE, Gonçalves MS, Soares MC, Menezes R, Saad ST, Costa FF. Arruda VR, et al. Among authors: goncalves ms. Clin Genet. 1998 Sep;54(3):210-4. doi: 10.1111/j.1399-0004.1998.tb04286.x. Clin Genet. 1998. PMID: 9788723

6

The Agamma-195 (C-->G) mutation in hereditary persistence of fetal hemoglobin is not associated with activation of a reporter gene in vitro.

Schreiber R, Gonçalves MS, Junqueira ML, Saad ST, Krieger JE, Costa FF. Schreiber R, et al. Among authors: goncalves ms. Braz J Med Biol Res. 2001 Apr;34(4):489-92. doi: 10.1590/s0100-879x2001000400008. Braz J Med Biol Res. 2001. PMID: 11285460 Free article.

7

Genetic variability of platelet glycoprotein Ibalpha gene.

Ozelo MC, Costa DS, Siqueira LH, Machado TM, Castro V, Gonçalves MS, Menezes RC, Soares M, Annichino-Bizzacchi JM, Costa FF, Arruda VR. Ozelo MC, et al. Among authors: goncalves ms. Am J Hematol. 2004 Oct;77(2):107-16. doi: 10.1002/ajh.20148. Am J Hematol. 2004. PMID: 15389918 Free article.

8

Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease.

Arruda VR, Annichino-Bizzacchi JM, Gonçalves MS, Costa FF. Arruda VR, et al. Among authors: goncalves ms. Thromb Haemost. 1997 Dec;78(6):1430-3. Thromb Haemost. 1997. PMID: 9423789

9

Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil.

Arruda VR, Siqueira LH, Gonçalves MS, von Zuben PM, Soares MC, Menezes R, Annichino-Bizzacchi JM, Costa FF. Arruda VR, et al. Among authors: goncalves ms. Am J Med Genet. 1998 Jul 24;78(4):332-5. doi: 10.1002/(sici)1096-8628(19980724)78:4<332::aid-ajmg5>3.0.co;2-n. Am J Med Genet. 1998. PMID: 9714434

10

Frequencies of platelet-specific alloantigen systems 1-5 in three distinct ethnic groups in Brazil.

Castro V, Origa AF, Annichino-Bizzacchi JM, Soares M, Menezes RC, Gonçalves MS, Costa FF, Arruda VR. Castro V, et al. Among authors: goncalves ms. Eur J Immunogenet. 1999 Oct;26(5):355-60. doi: 10.1046/j.1365-2370.1999.00174.x. Eur J Immunogenet. 1999. PMID: 10553502

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