Hans D. Saeger

Seven novel MLH1 and MSH2 germline mutations in hereditary nonpolyposis colorectal cancer.

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation.

Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.

Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability.

Identification of six novel MSH2 and MLH1 germline mutations in HNPCC.

Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression.

Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.

The rare case of a symptomatic atherosclerotic aneurysm of the superior epigastric artery mimicking an acute cholecystitis.

Tissue inhibitor of metalloproteinase-1 (TIMP-1) polymorphisms in a Caucasian population with abdominal aortic aneurysm.

Sensitive detection of colorectal cancer in peripheral blood by septin 9 DNA methylation assay.

Neuroendocrine tumors of the pancreas.

Who profits from neoadjuvant radiochemotherapy for locally advanced esophageal carcinoma?

Intraductal papillary mucinous tumors of the pancreas: biology, diagnosis, and treatment.