Costa FF - Search Results

1

Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosis.

Melo MB, Ahmad NN, Lima CS, Pagnano KB, Bordin S, Lorand-Metze I, SaAd ST, Costa FF. Melo MB, et al. Among authors: costa ff. Hematology. 2002 Feb;7(1):13-9. doi: 10.1080/10245330290020090. Hematology. 2002. PMID: 12171773 Free article.

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

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

4

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.

5

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

6

[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.

7

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

8

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.

9

Identification of Hb Zürich [alpha 2 beta 2(63)(E7)His-->Arg] by DNA analysis in a Brazilian family.

Miranda SR, Kimura EM, Saad ST, Costa FF. Miranda SR, et al. Among authors: costa ff. Hemoglobin. 1994 Sep;18(4-5):337-41. doi: 10.3109/03630269408996200. Hemoglobin. 1994. PMID: 7852089 No abstract available.

10

Hairy-cell leukemia and glucose-6-phosphate dehydrogenase.

Arruda VR, Saad ST, Costa FF. Arruda VR, et al. Among authors: costa ff. Acta Oncol. 1994;33(5):574. Acta Oncol. 1994. PMID: 7917374 No abstract available.

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