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49 results

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Page 1
DNA Methylation of Tumor Suppressor Genes in Pituitary Neuroendocrine Tumors.
García-Martínez A, Sottile J, Sánchez-Tejada L, Fajardo C, Cámara R, Lamas C, Barberá VM, Picó A. García-Martínez A, et al. Among authors: barbera vm. J Clin Endocrinol Metab. 2019 Apr 1;104(4):1272-1282. doi: 10.1210/jc.2018-01856. J Clin Endocrinol Metab. 2019. PMID: 30423170
Lack of cytomegalovirus detection in human glioma.
Garcia-Martinez A, Alenda C, Irles E, Ochoa E, Quintanar T, Rodriguez-Lescure A, Soto JL, Barbera VM. Garcia-Martinez A, et al. Among authors: barbera vm. Virol J. 2017 Nov 7;14(1):216. doi: 10.1186/s12985-017-0885-3. Virol J. 2017. PMID: 29116009 Free PMC article.
Utility of p16 immunohistochemistry for the identification of Lynch syndrome.
Payá A, Alenda C, Pérez-Carbonell L, Rojas E, Soto JL, Guillén C, Castillejo A, Barberá VM, Carrato A, Castells A, Llor X, Andreu M, Koh J, Enders GH, Benlloch S, Jover R. Payá A, et al. Among authors: barbera vm. Clin Cancer Res. 2009 May 1;15(9):3156-62. doi: 10.1158/1078-0432.CCR-08-3116. Epub 2009 Apr 21. Clin Cancer Res. 2009. PMID: 19383812 Free PMC article.
Clinically important molecular features of Peruvian colorectal tumours: high prevalence of DNA mismatch repair deficiency and low incidence of KRAS mutations.
Egoavil CM, Montenegro P, Soto JL, Casanova L, Sanchez-Lihon J, Castillejo MI, Martinez-Canto A, Perez-Carbonell L, Castillejo A, Guarinos C, Barbera VM, Jover R, Paya A, Alenda C. Egoavil CM, et al. Among authors: barbera vm. Pathology. 2011 Apr;43(3):228-33. doi: 10.1097/PAT.0b013e3283437613. Pathology. 2011. PMID: 21436632
Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer.
Castillejo A, Hernández-Illán E, Rodriguez-Soler M, Pérez-Carbonell L, Egoavil C, Barberá VM, Castillejo MI, Guarinos C, Martínez-de-Dueñas E, Juan MJ, Sánchez-Heras AB, García-Casado Z, Ruiz-Ponte C, Brea-Fernández A, Juárez M, Bujanda L, Clofent J, Llor X, Andreu M, Castells A, Carracedo A, Alenda C, Payá A, Jover R, Soto JL. Castillejo A, et al. Among authors: barbera vm. J Med Genet. 2015 Jul;52(7):498-502. doi: 10.1136/jmedgenet-2015-103076. Epub 2015 Apr 23. J Med Genet. 2015. PMID: 25908759
Molecular biology of exocrine pancreatic cancer.
Soto JL, Barbera VM, Saceda M, Carrato A. Soto JL, et al. Among authors: barbera vm. Clin Transl Oncol. 2006 May;8(5):306-12. doi: 10.1007/s12094-006-0175-9. Clin Transl Oncol. 2006. PMID: 16760004 Review.
Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.
Pérez-Carbonell L, Alenda C, Payá A, Castillejo A, Barberá VM, Guillén C, Rojas E, Acame N, Gutiérrez-Aviñó FJ, Castells A, Llor X, Andreu M, Soto JL, Jover R. Pérez-Carbonell L, et al. Among authors: barbera vm. J Mol Diagn. 2010 Jul;12(4):498-504. doi: 10.2353/jmoldx.2010.090212. Epub 2010 May 20. J Mol Diagn. 2010. PMID: 20489114 Free PMC article.
EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients.
Guarinos C, Castillejo A, Barberá VM, Pérez-Carbonell L, Sánchez-Heras AB, Segura A, Guillén-Ponce C, Martínez-Cantó A, Castillejo MI, Egoavil CM, Jover R, Payá A, Alenda C, Soto JL. Guarinos C, et al. Among authors: barbera vm. J Mol Diagn. 2010 Nov;12(6):765-70. doi: 10.2353/jmoldx.2010.100039. Epub 2010 Sep 23. J Mol Diagn. 2010. PMID: 20864635 Free PMC article.
Recurrent testicular germ cell tumors in a family with MYH-associated polyposis.
Castillejo A, Sanchez-Heras AB, Jover R, Castillejo MI, Guarinos C, Oltra S, Martínez-Canto A, Barbera VM, Laforga J, Paya A, Alenda C, Soto JL. Castillejo A, et al. Among authors: barbera vm. J Clin Oncol. 2012 Aug 10;30(23):e216-7. doi: 10.1200/JCO.2012.41.5992. Epub 2012 Jun 18. J Clin Oncol. 2012. PMID: 22711856 No abstract available.
49 results