Annichino-Bizzacchi JM - Search Results

1

Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk.

Lima CS, Ortega MM, Ozelo MC, Araujo RC, De Souza CA, Lorand-Metze I, Annichino-Bizzacchi JM, Costa FF. Lima CS, et al. Leuk Res. 2008 Mar;32(3):401-5. doi: 10.1016/j.leukres.2007.06.001. Epub 2007 Jul 25. Leuk Res. 2008. PMID: 17655928

2

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. Blood. 1995 Oct 15;86(8):3015-20. Blood. 1995. PMID: 7579394 Free article.

3

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

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

4

[Detection of hemophilia A gene carriers in a Brazilian population].

Arruda VR, Annichino-Bizzacchi JM, Costa FF. Arruda VR, et al. Rev Assoc Med Bras (1992). 1993 Jul-Sep;39(3):126-30. Rev Assoc Med Bras (1992). 1993. PMID: 7904214 Portuguese.

5

The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.

Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzacchi JM, Costa FF. Arruda VR, et al. Thromb Haemost. 1997 May;77(5):818-21. Thromb Haemost. 1997. PMID: 9184384

6

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. Thromb Haemost. 1997 Dec;78(6):1430-3. Thromb Haemost. 1997. PMID: 9423789

7

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. 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

8

Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.

Andrade FL, Annichino-Bizzacchi JM, Saad ST, Costa FF, Arruda VR. Andrade FL, et al. Am J Hematol. 1998 Sep;59(1):46-50. doi: 10.1002/(sici)1096-8652(199809)59:1<46::aid-ajh9>3.0.co;2-#. Am J Hematol. 1998. PMID: 9723576 Free article.

9

Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease.

Arruda VR, Belangero WD, Ozelo MC, Oliveira GB, Pagnano RG, Volpon JB, Annichino-Bizzacchi JM. Arruda VR, et al. J Pediatr Orthop. 1999 Jan-Feb;19(1):84-7. J Pediatr Orthop. 1999. PMID: 9890294

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. 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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