Zobrazeno 1 - 5
of 5
pro vyhledávání: '"J. H.P. Wilson"'
Autor:
Johan J.P. Gille, Fred H. Menko, Gabriela Möslein, Francis M. Giardiello, Wendy Lim, G. J. A. Offerhaus, Allan D. Spigelman, Anne Marie Westerman, Stephen B. Gruber, Felix W. M. de Rooij, N Hearle, T. Vogel, Robin K. S. Phillips, J. H.P. Wilson, Valérie Schumacher, J J Keller, Lisa A. Boardman, Jill D. Trimbath, B. Royer-Pokora, Richard S. Houlston, Rodney J. Scott, Anika Hansmann, Sylviane Olschwang
Publikováno v:
Hearle, N, Schumacher, V, Menko, F H, Olschwang, S, Boardman, L A, Gille, J J P, Keller, J J, Westerman, A M, Scott, R J, Lim, W, Trimbath, J D, Giardiello, F M, Gruber, S B, Offerhaus, G J A, Rooij, F W M D E, Wilson, J H P, Hansmann, A, Möslein, G, Royer-Pokora, B, Vogel, T, Phillips, R K S, Spigelman, A D & Houlston, R S 2006, ' STK11 status and intussusception risk in Peutz-Jeghers syndrome ', Journal of Medical Genetics, vol. 43, no. 8, pp. e41 . https://doi.org/10.1136/jmg.2005.040535
Journal of Medical Genetics, 43(8). BMJ Publishing Group
Journal of medical genetics, 43(8). BMJ Publishing Group
Journal of Medical Genetics, 43(8). BMJ Publishing Group
Journal of medical genetics, 43(8). BMJ Publishing Group
BACKGROUND: Peutz-Jeghers syndrome (PJS) is caused by germline STK11 mutations and characterised by gastrointestinal polyposis. Although small bowel intussusception is a recognised complication of PJS, risk varies between patients.OBJECTIVE: To analy
Autor:
J. H.P. Wilson, Francis M. Giardiello, M.L.F. van Velthuysen, G. J. A. Offerhaus, J J Keller, B P van Rees, A.F.P.M. de Goeij, Anne Marie Westerman, Mark M. Entius
Publikováno v:
Journal of clinical pathology, 54(2), 126-131. BMJ Publishing Group
Journal of Clinical Pathology, 54, 126-131. BMJ Publishing Group
Journal of Clinical Pathology, 54, 126-131. BMJ Publishing Group
Aim—To investigate whether mutations in the STK11/LKB1 gene and genes implicated in the colorectal adenoma–carcinoma sequence are involved in Peutz-Jeghers syndrome (PJS) related tumorigenesis. Methods—Thirty nine polyps and five carcinomas fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::950dfcd7222740d1352a8a922974b7ed
https://pure.amc.nl/en/publications/molecular-genetic-alterations-in-hamartomatous-polyps-and-carcinomas-of-patients-with-peutzjeghers-syndrome(a7261c74-0340-4a46-bad1-c2b17fffe8d2).html
https://pure.amc.nl/en/publications/molecular-genetic-alterations-in-hamartomatous-polyps-and-carcinomas-of-patients-with-peutzjeghers-syndrome(a7261c74-0340-4a46-bad1-c2b17fffe8d2).html
Autor:
Stanley R. Hamilton, M.L.F. van Velthuysen, J. H.P. Wilson, Francis M. Giardiello, G. J. A. Offerhaus, Robbert J.C. Slebos, Anne Marie Westerman, Mark M. Entius, M. M. Polak
Publikováno v:
Gut, 41, 320-322. BMJ Publishing Group
Gut, 41(3), 320-322. BMJ Publishing Group
Gut, 41(3), 320-322. BMJ Publishing Group
Background—Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant, polyposis syndrome, associated with an increased risk of gastrointestinal and extragastrointestinal malignancy. Occasionally dysplasia occurs in PJS polyps.Aims—In colorectal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca9b914528fe13d815b3cb33b93cb74e
https://dare.uva.nl/personal/pure/en/publications/peutzjeghers-polyps-dysplasia-and-kras-codon-12-mutations(09cc946f-4593-47b5-84ec-dd05d130c0fe).html
https://dare.uva.nl/personal/pure/en/publications/peutzjeghers-polyps-dysplasia-and-kras-codon-12-mutations(09cc946f-4593-47b5-84ec-dd05d130c0fe).html
Publikováno v:
European Journal of Gastroenterology & Hepatology. 11:A29
Autor:
G. J. A. Offerhaus, Mark M. Entius, J. H.P. Wilson, Anne Marie Westerman, Dick Lindhout, J. W.W. Coebergh, M. L.F. van Velthuysen
Publikováno v:
European Journal of Gastroenterology & Hepatology. 10:A42