Lista de obras -

Absence of deleterious palladin mutations in patients with familial pancreatic cancer.

artículo científico publicado en 2009

Absence of germline BRCA1 mutations in familial pancreatic cancer patients

artículo científico publicado en 2009

Age- and disease-related methylation of multiple genes in nonneoplastic duodenum and in duodenal juice.

artículo científico publicado en 2005

Assessment of "gene-environment" interaction in cases of familial and sporadic pancreatic cancer

artículo científico publicado en 2009

Clinical importance of precursor lesions in the pancreas

artículo científico publicado en 2007

Copy-number variants in patients with a strong family history of pancreatic cancer

article

Elevated cancer mortality in the relatives of patients with pancreatic cancer

artículo científico publicado en 2009

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

artículo científico publicado en 2009

Genetic and epigenetic alterations of familial pancreatic cancers

artículo científico publicado en 2008

Genome-wide allelotypes of familial pancreatic adenocarcinomas and familial and sporadic intraductal papillary mucinous neoplasms

artículo científico publicado en 2007

Increased prevalence of the BRCA2 polymorphic stop codon K3326X among individuals with familial pancreatic cancer

artículo científico publicado en 2005

Methylation of cyclin D2 is observed frequently in pancreatic cancer but is also an age-related phenomenon in gastrointestinal tissues

artículo científico publicado en 2003

Multifocal neoplastic precursor lesions associated with lobular atrophy of the pancreas in patients having a strong family history of pancreatic cancer.

artículo científico publicado en 2006

Polymorphisms of SPINK1 N34S and CFTR in patients with sporadic and familial pancreatic cancer

artículo científico publicado en 2003

Prospective risk of pancreatic cancer in familial pancreatic cancer kindreds

artículo científico publicado en 2004

Screening for early pancreatic neoplasia in high-risk individuals: a prospective controlled study.

artículo científico publicado en 2006

Screening for pancreatic neoplasia in high-risk individuals: an EUS-based approach

artículo científico publicado en 2004

The genetics of FANCC and FANCG in familial pancreatic cancer

artículo científico publicado en 2004

The prevalence of BRCA2 mutations in familial pancreatic cancer

scientific article published on 01 February 2007

Lista de obras de

Absence of deleterious palladin mutations in patients with familial pancreatic cancer.

Absence of germline BRCA1 mutations in familial pancreatic cancer patients

Age- and disease-related methylation of multiple genes in nonneoplastic duodenum and in duodenal juice.

Assessment of "gene-environment" interaction in cases of familial and sporadic pancreatic cancer

Clinical importance of precursor lesions in the pancreas

Copy-number variants in patients with a strong family history of pancreatic cancer

Elevated cancer mortality in the relatives of patients with pancreatic cancer

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

Genetic and epigenetic alterations of familial pancreatic cancers

Genome-wide allelotypes of familial pancreatic adenocarcinomas and familial and sporadic intraductal papillary mucinous neoplasms

Increased prevalence of the BRCA2 polymorphic stop codon K3326X among individuals with familial pancreatic cancer

Methylation of cyclin D2 is observed frequently in pancreatic cancer but is also an age-related phenomenon in gastrointestinal tissues

Multifocal neoplastic precursor lesions associated with lobular atrophy of the pancreas in patients having a strong family history of pancreatic cancer.

Polymorphisms of SPINK1 N34S and CFTR in patients with sporadic and familial pancreatic cancer

Prospective risk of pancreatic cancer in familial pancreatic cancer kindreds

Screening for early pancreatic neoplasia in high-risk individuals: a prospective controlled study.

Screening for pancreatic neoplasia in high-risk individuals: an EUS-based approach

The genetics of FANCC and FANCG in familial pancreatic cancer

The prevalence of BRCA2 mutations in familial pancreatic cancer