Search Results - "Entius, MM"

Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome by Entius, M M, Keller, J J, Westerman, A M, van Rees, B P, van Velthuysen, M-L F, de Goeij, A F P M, Wilson, J H P, Giardiello, F M, Offerhaus, G J A

“…Aim—To investigate whether mutations in the STK11/LKB1 gene and genes implicated in the colorectal adenoma–carcinoma sequence are involved in Peutz-Jeghers…”
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Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy by VAN TINTELEN, J. Peter, ENTIUS, Mark M, HOFSTRA, Robert M. W, OTTERSPOOR, Luuk C, DOEVENDANS, Pieter A. F. M, RODRIGUEZ, Luz-Maria, VAN GELDER, Isabelle C, HAUER, Richard N. W, BHUIYAN, Zahurul A, JONGBLOED, Roselie, WIESFELD, Ans C. P, WILDE, Arthur A. M, VAN DER SMAGT, Jasper, BOVEN, Ludolf G, MANNENS, Marcel M. A. M, VAN LANGEN, Irene M

“…Mutations in the plakophilin-2 gene (PKP2) have been found in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC). Hence, genetic…”
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Germline and Somatic Mutations of the STK11/LKB1 Peutz-Jeghers Gene in Pancreatic and Biliary Cancers by Su, Gloria H., Hruban, Ralph H., Bansal, Ravi K., Bova, G. Steven, Tang, David J., Shekher, Manu C., Westerman, Anne Marie, Entius, Mark M., Goggins, Michael, Yeo, Charles J., Kern, Scott E.

“…Peutz-Jeghers syndrome (PJS) is an autosomal-dominant disorder characterized by hamartomatous polyps in the gastrointestinal tract and by pigmented macules of…”
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Multiple hyperplastic polyps in the stomach: Evidence for clonality and neoplastic potential by Dijkhuizen, SM, Entius, MM, Clement, MJ, Polak, MM, Van den Berg, FM, Craanen, ME, Slebos, RJ, Offerhaus, GJ

“…The origin and neoplastic potential of gastric epithelial polyps remains an area of great interest, and treatment choices are a topic of controversy. This…”
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Microsatellite Instability and Expression of hMLH-1 and hMSH-2 in Sebaceous Gland Carcinomas as Markers for Muir-Torre Syndrome by Entius, M M, Keller, J J, Drillenburg, P, Kuypers, K C, Giardiello, F M, Offerhaus, G J

“…Sebaceous gland carcinomas (SGCs) are rare malignant skin tumors occurring sporadically or as a phenotypic feature of the Muir-Torre syndrome (MTS). A subset…”
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Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome by GRUBER, S. B, ENTIUS, M. M, VOGELSTEIN, B, HAMILTON, S. R, POLYMEROPOULOS, M. H, OFFERHAUS, G. J, GIARDIELLO, F. M, PETERSEN, G. M, LAKEN, S. J, LONGO, P. A, BOYER, R, LEVIN, A. M, MUJUMDAR, U. J, TRENT, J. M, KINZLER, K. W

“…Peutz-Jeghers syndrome (PJS) is an autosomal dominant condition characterized by intestinal hamartomatous polyps, mucocutaneous melanin deposition, and…”
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Peutz-Jeghers syndrome: 78-year follow-up of the original family by Westerman, Anne Marie, Entius, Mark M, de Baar, Ellen, Boor, Patrick PC, Koole, Rita, van Velthuysen, M Loes F, Offerhaus, G Johan A, Lindhout, Dick, de Rooij, Felix WM, Wilson, JH Paul

“…The association between heredity, gastrointestinal polyposis, and mucocutaneous pigmentation in Peutz-Jeghers syndrome (PJS) was first recognised in 1921 by…”
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Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families by Westerman, Anne Marie, Entius, Mark M., Boor, Patrick P.C., Koole, Rita, Baar, Ellen de, Offerhaus, G. Johan A., Lubinski, Jan, Lindhout, Dick, Halley, Dicky J.J., de Rooij, Felix W.M., Wilson, J.H. Paul

“…The Peutz‐Jeghers syndrome (PJS) is a rare hereditary disorder in which gastrointestinal hamartomatous polyposis, mucocutaneous pigmentation, and a…”
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Upper gastrointestinal polyps in familial adenomatous polyposis by Offerhaus, G J, Entius, M M, Giardiello, F M

“…Familial adenomatous polyposis (FAP) is an autosomal dominant disease in which affected family members develop numerous colorectal adenomas with a virtually…”
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Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract by Entius, M M, Westerman, A M, van Velthuysen, M L, Wilson, J H, Hamilton, S R, Giardiello, F M, Offerhaus, G J

“…Hamartomatous gastrointestinal polyposis syndromes have always been considered as non-neoplastic. Nevertheless, an increased cancer risk both within and…”
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Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations by Entius, M M, Westerman, A M, Giardiello, F M, van Velthuysen, M-L F, Polak, M M, Slebos, R J C, Wilson, J H P, Hamilton, S R, Offerhaus, G J A

“…Background—Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant, polyposis syndrome, associated with an increased risk of gastrointestinal and…”
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