A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

Por Mangold, E, Pagenstecher, C, Leister, M, Mathiak, M, Rutten, A, Friedl, W, Propping, P, Ruzicka, T, Kruse, R
Publicado em 2004

Members of the EpCAM signalling pathway are expressed in gastric cancer tissue and are correlated with patient prognosis

Por Warneke, V S, Behrens, H-M, Haag, J, Krüger, S, Simon, E, Mathiak, M, Ebert, M P A, Röcken, C
Publicado em 2013

Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with col...

Por Lamberti, C, Kruse, R, Ruelfs, C, Caspari, R, Wang, Y, Jungck, M, Mathiak, M, Malayeri, H, Friedl, W, Sauerbruch, T, Propping, P
Publicado em 1999

Rare Benign Entities of the Breast – Myoid Hamartoma and Capillary Hemangioma

Por Schäfer, F. K., Biernath-Wuepping, J., Eckmann-Scholz, C., Order, B. M., Mathiak, M., Hilpert, F., Strauss, A., Jonat, W., Schäfer, P. J.
Publicado em 2012

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Por Kruse, R, Rütten, A, Lamberti, C, Hosseiny-Malayeri, H R, Wang, Y, Ruelfs, C, Jungck, M, Mathiak, M, Ruzicka, T, Hartschuh, W, Bisceglia, M, Friedl, W, Propping, P
Publicado em 1998