Bizarro S - Search Results

1

Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician origin.

Santos C, Peixoto A, Rocha P, Vega A, Soares MJ, Cerveira N, Bizarro S, Pinheiro M, Pereira D, Rodrigues H, Castro F, Henrique R, Teixeira MR. Santos C, et al. Among authors: bizarro s. Fam Cancer. 2009;8(3):203-8. doi: 10.1007/s10689-008-9229-1. Epub 2009 Jan 3. Fam Cancer. 2009. PMID: 19123044

2

Highly sensitive detection of the MGB1 transcript (mammaglobin) in the peripheral blood of breast cancer patients.

Cerveira N, Torres L, Rocha P, Bizarro S, Pereira D, Abreu J, Henrique R, Teixeira MR, Castedo S. Cerveira N, et al. Among authors: bizarro s. Int J Cancer. 2004 Feb 10;108(4):592-5. doi: 10.1002/ijc.11609. Int J Cancer. 2004. PMID: 14696125

3

Pathogenicity evaluation of BRCA1 and BRCA2 unclassified variants identified in Portuguese breast/ovarian cancer families.

Santos C, Peixoto A, Rocha P, Pinto P, Bizarro S, Pinheiro M, Pinto C, Henrique R, Teixeira MR. Santos C, et al. Among authors: bizarro s. J Mol Diagn. 2014 May;16(3):324-34. doi: 10.1016/j.jmoldx.2014.01.005. Epub 2014 Mar 5. J Mol Diagn. 2014. PMID: 24607278 Free article.

4

The role of targeted BRCA1/BRCA2 mutation analysis in hereditary breast/ovarian cancer families of Portuguese ancestry.

Peixoto A, Santos C, Pinto P, Pinheiro M, Rocha P, Pinto C, Bizarro S, Veiga I, Principe AS, Maia S, Castro F, Couto R, Gouveia A, Teixeira MR. Peixoto A, et al. Among authors: bizarro s. Clin Genet. 2015 Jul;88(1):41-8. doi: 10.1111/cge.12441. Epub 2014 Jul 26. Clin Genet. 2015. PMID: 24916970

5

Multimodal genetic diagnosis of solid variant alveolar rhabdomyosarcoma.

Cerveira N, Torres L, Ribeiro FR, Henrique R, Pinto A, Bizarro S, Ferreira AM, Lopes C, Teixeira MR. Cerveira N, et al. Among authors: bizarro s. Cancer Genet Cytogenet. 2005 Dec;163(2):138-43. doi: 10.1016/j.cancergencyto.2005.06.020. Cancer Genet Cytogenet. 2005. PMID: 16337856

6

Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemia.

Bizarro S, Cerveira N, Correia C, Lisboa S, Peixoto A, Norton L, Teixeira MR. Bizarro S, et al. Cancer Genet Cytogenet. 2007 Oct 1;178(1):61-4. doi: 10.1016/j.cancergencyto.2007.05.023. Cancer Genet Cytogenet. 2007. PMID: 17889710

7

Molecular diagnosis of the Portuguese founder mutation BRCA2 c.156_157insAlu.

Peixoto A, Santos C, Rocha P, Pinto P, Bizarro S, Teixeira MR. Peixoto A, et al. Among authors: bizarro s. Breast Cancer Res Treat. 2009 Sep;117(1):215-7. doi: 10.1007/s10549-008-0214-z. Epub 2008 Oct 14. Breast Cancer Res Treat. 2009. PMID: 18853249 No abstract available.

8

Coexistence of alternative MLL-SEPT9 fusion transcripts in an acute myeloid leukemia with t(11;17)(q23;q25).

Santos J, Cerveira N, Correia C, Lisboa S, Pinheiro M, Torres L, Bizarro S, Vieira J, Viterbo L, Mariz JM, Teixeira MR. Santos J, et al. Among authors: bizarro s. Cancer Genet Cytogenet. 2010 Feb;197(1):60-4. doi: 10.1016/j.cancergencyto.2009.10.010. Cancer Genet Cytogenet. 2010. PMID: 20113838

9

A novel spliced fusion of MLL with CT45A2 in a pediatric biphenotypic acute leukemia.

Cerveira N, Meyer C, Santos J, Torres L, Lisboa S, Pinheiro M, Bizarro S, Correia C, Norton L, Marschalek R, Teixeira MR. Cerveira N, et al. Among authors: bizarro s. BMC Cancer. 2010 Sep 29;10:518. doi: 10.1186/1471-2407-10-518. BMC Cancer. 2010. PMID: 20920256 Free PMC article.

10

Acute megakaryoblastic leukemia with a four-way variant translocation originating the RBM15-MKL1 fusion gene.

Torres L, Lisboa S, Vieira J, Cerveira N, Santos J, Pinheiro M, Correia C, Bizarro S, Almeida M, Teixeira MR. Torres L, et al. Among authors: bizarro s. Pediatr Blood Cancer. 2011 May;56(5):846-9. doi: 10.1002/pbc.22765. Epub 2011 Jan 13. Pediatr Blood Cancer. 2011. PMID: 21370421

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