Rodrigues P - Search Results

1

Men seeking counselling in a Breast Cancer Risk Evaluation Clinic.

Freitas AC, Opinião A, Fragoso S, Nunes H, Santos M, Clara A, Bento S, Luis A, Silva J, Moura C, Filipe B, Machado P, Santos S, André S, Rodrigues P, Parreira J, Vaz F. Freitas AC, et al. Among authors: rodrigues p. Ecancermedicalscience. 2018 Jan 30;12:804. doi: 10.3332/ecancer.2018.804. eCollection 2018. Ecancermedicalscience. 2018. PMID: 29456621 Free PMC article.

2

Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes.

Machado PM, Brandão RD, Cavaco BM, Eugénio J, Bento S, Nave M, Rodrigues P, Fernandes A, Vaz F. Machado PM, et al. Among authors: rodrigues p. J Clin Oncol. 2007 May 20;25(15):2027-34. doi: 10.1200/JCO.2006.06.9443. J Clin Oncol. 2007. PMID: 17513806

3

[MYH associated polyposis: severe phenotype in the homozygosity for the 1103delC mutation].

De Ferro SM, Lage P, Suspiro A, Fidalgo P, Fragoso S, Baltazar C, Vitoriano I, Rodrigues P, Albuquerque C, Leitão CN. De Ferro SM, et al. Among authors: rodrigues p. Acta Med Port. 2007 May-Jun;20(3):243-7. Epub 2007 Jul 2. Acta Med Port. 2007. PMID: 17868535 Free article. Portuguese.

4

[Need of new clinical criteria for the identification of genetic Lynch syndrome].

Sousa R, Lage P, Ferreira S, Claro I, Francisco I, Filipe B, Albuquerque C, Suspiro A, Rodrigues P, Nobre-Leitão C. Sousa R, et al. Among authors: rodrigues p. Acta Med Port. 2007 Nov-Dec;20(6):535-42. Epub 2008 Feb 13. Acta Med Port. 2007. PMID: 18331697 Free article. Portuguese.

5

Aggressive phenotype of MYH-associated polyposis with jejunal cancer and intra-abdominal desmoid tumor: report of a case.

de Ferro SM, Suspiro A, Fidalgo P, Lage P, Rodrigues P, Fragoso S, Vitoriano I, Baltazar C, Albuquerque C, Bettencourt A, Leitão CN. de Ferro SM, et al. Among authors: rodrigues p. Dis Colon Rectum. 2009 Apr;52(4):742-5. doi: 10.1007/DCR.0b013e318199db93. Dis Colon Rectum. 2009. PMID: 19404084

6

APC somatic mosaicism in a patient with Gardner syndrome carrying the E1573X mutation: report of a case.

Filipe B, Albuquerque C, Bik E, Lage P, Rodrigues P, Vossen R, Tops C, Nobre Leitão C. Filipe B, et al. Among authors: rodrigues p. Dis Colon Rectum. 2009 Aug;52(8):1516-20; discussion 1520-1. doi: 10.1007/DCR.0b013e3181ab810f. Dis Colon Rectum. 2009. PMID: 19617769

7

[Familial colorectal cancer type X: clinical, pathological and molecular characterization].

Ferreira S, Lage P, Sousa R, Claro I, Francisco I, Filipe B, Suspiro A, Chaves P, Rodrigues P, Albuquerque C, Nobre Leitão C. Ferreira S, et al. Among authors: rodrigues p. Acta Med Port. 2009 May-Jun;22(3):207-14. Epub 2009 Jul 15. Acta Med Port. 2009. PMID: 19686620 Free article. Portuguese.

8

APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.

Filipe B, Baltazar C, Albuquerque C, Fragoso S, Lage P, Vitoriano I, Mão de Ferro S, Claro I, Rodrigues P, Fidalgo P, Chaves P, Cravo M, Nobre Leitão C. Filipe B, et al. Among authors: rodrigues p. Clin Genet. 2009 Sep;76(3):242-55. doi: 10.1111/j.1399-0004.2009.01241.x. Clin Genet. 2009. PMID: 19793053

9

Colorectal cancers show distinct mutation spectra in members of the canonical WNT signaling pathway according to their anatomical location and type of genetic instability.

Albuquerque C, Baltazar C, Filipe B, Penha F, Pereira T, Smits R, Cravo M, Lage P, Fidalgo P, Claro I, Rodrigues P, Veiga I, Ramos JS, Fonseca I, Leitão CN, Fodde R. Albuquerque C, et al. Among authors: rodrigues p. Genes Chromosomes Cancer. 2010 Aug;49(8):746-59. doi: 10.1002/gcc.20786. Genes Chromosomes Cancer. 2010. PMID: 20544848

10

Familial colorectal cancer type X syndrome: two distinct molecular entities?

Francisco I, Albuquerque C, Lage P, Belo H, Vitoriano I, Filipe B, Claro I, Ferreira S, Rodrigues P, Chaves P, Leitão CN, Pereira AD. Francisco I, et al. Among authors: rodrigues p. Fam Cancer. 2011 Dec;10(4):623-31. doi: 10.1007/s10689-011-9473-7. Fam Cancer. 2011. PMID: 21837511

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