Costa FF - Search Results

1

Mutation analysis of the HFE gene in Brazilian populations.

Agostinho MF, Arruda VR, Basseres DS, Bordin S, Soares MC, Menezes RC, Costa FF, Saad ST. Agostinho MF, et al. Among authors: costa ff. Blood Cells Mol Dis. 1999 Oct-Dec;25(5-6):324-7. doi: 10.1006/bcmd.1999.0260. Blood Cells Mol Dis. 1999. PMID: 10660479

2

Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Brazil.

Saad ST, Costa FF. Saad ST, et al. Among authors: costa ff. Hum Hered. 1992;42(2):125-8. doi: 10.1159/000154052. Hum Hered. 1992. PMID: 1572671

3

Hemoglobin Bart's in a Brazilian black population.

Sonati MF, Costa FF. Sonati MF, et al. Among authors: costa ff. Braz J Med Biol Res. 1990;23(5):395-6. Braz J Med Biol Res. 1990. PMID: 2095287

4

Hepatitis C antibody (anti-HCV) prevalence in Brazilian patients with sickle cell diseases.

Arruda VR, Eid KA, Zen GC, Gonçales NS, Saad ST, Costa FF. Arruda VR, et al. Among authors: costa ff. Vox Sang. 1993;65(3):247. doi: 10.1111/j.1423-0410.1993.tb02161.x. Vox Sang. 1993. PMID: 7504375 No abstract available.

5

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. Among authors: costa ff. Ann Hematol. 1995 Mar;70(3):159-61. doi: 10.1007/BF01682037. Ann Hematol. 1995. PMID: 7536477

6

Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients.

Arruda VR, Pieneman WC, Reitsma PH, Deutz-Terlouw PP, Annichino-Bizzacchi JM, Briët E, Costa FF. Arruda VR, et al. Among authors: costa ff. Blood. 1995 Oct 15;86(8):3015-20. Blood. 1995. PMID: 7579394 Free article.

7

Factor V Leiden (FVQ 506) is common in a Brazilian population.

Arruda VR, Annichino-Bizzacchi JM, Costa FF, Reitsma PH. Arruda VR, et al. Among authors: costa ff. Am J Hematol. 1995 Jul;49(3):242-3. doi: 10.1002/ajh.2830490312. Am J Hematol. 1995. PMID: 7604818

8

[Molecular aspects of erythrocyte membrane disorders].

Saad ST, Costa FF. Saad ST, et al. Among authors: costa ff. Rev Assoc Med Bras (1992). 1994 Jul-Sep;40(3):216-24. Rev Assoc Med Bras (1992). 1994. PMID: 7787875 Review. Portuguese. No abstract available.

9

Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil.

Saad ST, Costa FF, Vicentim DL, Salles TS, Pranke PH. Saad ST, et al. Among authors: costa ff. Br J Haematol. 1994 Oct;88(2):295-9. doi: 10.1111/j.1365-2141.1994.tb05021.x. Br J Haematol. 1994. PMID: 7803273

10

Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysis.

Saad ST, Costa FF, Salles TS, Sonatti MF, Figueiredo MS. Saad ST, et al. Among authors: costa ff. Blood. 1995 Jan 15;85(2):601-2. Blood. 1995. PMID: 7812018 Free article. No abstract available.

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