Zobrazeno 1 - 10
of 29
pro vyhledávání: '"G. Moslein"'
Autor:
G.M. Cavestro, A. Mannucci, F. Balaguer, H. Heather, S. Kupfer, A. Repici, A. Sartore-Bianchi, T. Seppala, V. Valentini, C. Boland, R. Brand, T. Buffart, C. Burke, R. Caccialanza, R. Cannizzaro, S. Cascinu, A. Cercek, E. Crosbie, S. Danese, E. Dekker, M. Daca-Alvarez, F. Deni, A. Latchford, D. Liska, P. Lynch, A. Malesci, G. Mauri, E. Meldolesi, M. Pal, K. Monahan, G. Moslein, C. Murphy, K. Nass, K. Ng, C. Oliani, E. Papaleo, S. Patel, M. Puzzono, A. Remo, L. Ricciardiello, C. Ripamonti, S. Siena, S. Singh, Z. Stadler, P. Stanich, S. Syngal, S. Turi, E. Urso, L. Valle, V. Vanni, E. Vilar, M. Vitellaro, Y. You, M. Yurgelun, R. Zuppardo, E. Stoffel
Publikováno v:
Digestive and Liver Disease. 55:S139-S140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9931baedee91f615e4c4d229327c7a6
https://doi.org/10.1016/s1590-8658(23)00349-3
https://doi.org/10.1016/s1590-8658(23)00349-3
Autor:
Monika Morak, Jacob Nattermann, Swetlana Ladigan-Badura, Wolff Schmiegel, Stefan Aretz, Markus Löffler, Elke Holinski-Feder, Karsten Schulmann, Christoph Engel, Christian Pox, Verena Steinke-Lange, Robert Hüneburg, Matthias Kloor, Jürgen Weitz, Judith Tomann, Christian P. Strassburg, Deepak Vangala, Huu Phuc Nguyen, Ali Canbay, G Moslein, Nils Rahner, Claudia Perne, Karolin Bucksch, Reinhard Büttner
Publikováno v:
International journal of cancerREFERENCES. 149(12)
Small bowel cancer (SBC) is the malignancy with the highest standardized incidence ratio in Lynch syndrome (LS) patients. Of all SBCs, about 50% are duodenal cancers (DCs), therefore being accessible by esophago-gastro-duodenoscopy (EGD) for surveill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::248e19345545553a510c045cafa4fa97
https://pubmed.ncbi.nlm.nih.gov/34331771
https://pubmed.ncbi.nlm.nih.gov/34331771
Autor:
Stefan Aretz, Saskia Haupt, Deepak Vangala, Steinke-Lange, Sieber-Frank J, Elizabeth Alwers, Heuveline, Hendrik Bläker, Juergen Weitz, von Knebel Doeberitz M, G Moslein, Aysel Ahadova, David Horst, Claudia Perne, Hans-Konrad Schackert, W. Schmiegel, Christoph Engel, Markus Löffler, von Winterfeld M, Robert Hüneburg, Jenny Chang-Claude, Matthias Kloor, Elke Holinski-Feder, H Brenner, Michael Hoffmeister, Monika Morak, Arnold A, Wilfried Roth, Florian Seidler, Nils Rahner
Background and aimsBRAFV600E mutations have been reported to be associated with sporadic microsatellite-unstable (MSI) colorectal cancer (CRC), while rarely detected in CRCs of Lynch syndrome (LS) patients. Therefore, current international diagnostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65ee2e8a4aac80a63109a359842db81f
Akademický článek
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Autor:
Karl Heinimann, G Moslein, I. J. Christensen, Ian Tomlinson, Steffen Bülow, Anne Lyster Knudsen
Publikováno v:
Colorectal Disease. 12:e243-e249
Aim The study aimed to describe genetical and clinical features of attenuated familial adenomatous polyposis (AFAP) and to propose clinical criteria and guidelines for treatment and surveillance. Method A questionnaire study was carried out of polypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee6221483d3cebe12551f2cadaeb9a9e
https://doi.org/10.1111/j.1463-1318.2010.02218.x
https://doi.org/10.1111/j.1463-1318.2010.02218.x
Autor:
Lucio Bertario, Yann Parc, Müller H, Christoph Engel, Astrid Stormorken, Angel Alonso, Peter Möller, Karl Heinimann, Hans F. A. Vasen, Frederik J. Hes, Fokko M. Nagengast, John A. Karagiannis, John Burn, M. Ponz de Leon, Stefan Aretz, Nils Rahner, Torben Myrhøj, Ignacio Blanco, Sabine Tejpar, Heikki Järvinen, E. Claes, Huw Thomas, Chrystelle Colas, Isis Dove-Edwin, Ian M. Frayling, Laura Renkonen-Sinisalo, Jan Lubinski, Jukka-Pekka Mecklin, Steffen Bülow, Inge Bernstein, Shirley Hodgson, Juul T. Wijnen, Annika Lindblom, Gabriel Capellá, G Moslein, Julian R. Sampson
Publikováno v:
Familial Cancer, 9(2), 109-115
Familial Cancer, 9, 2, pp. 109-15
Familial Cancer, 9, 109-15
Familial Cancer
Familial Cancer, 9, 2, pp. 109-15
Familial Cancer, 9, 109-15
Familial Cancer
Item does not contain fulltext Familial colorectal cancer (CRC) accounts for 10-15% of all CRCs. In about 5% of all cases, CRC is associated with a highly penetrant dominant inherited syndrome. The most common inherited form of non-polyposis CRC is t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af305ca4e2a2a135f6987991089c0ea9
https://doi.org/10.1007/s10689-009-9291-3
https://doi.org/10.1007/s10689-009-9291-3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
G Moslein, Ignacio Blanco, Yann Parc, Werner Friedl, Hans F. A. Vasen, Shirley Hodgson, M. Ponz de Leon, Astrid Stormorken, Susan K. Clark, Juul T. Wijnen, Mecklin Jp, Sabine Tejpar, Robin K. S. Phillips, Steffen Bülow, Frederik J. Hes, Chrystelle Colas, Peter Möller, W. Hyer, Heikki Järvinen, Huw Thomas, Gabriel Capellá, Andrew D Beggs, Julian R. Sampson, Laura Renkonen-Sinisalo, Angel Alonso, Andrew Latchford, Fokko M. Nagengast, John Burn, Stefan Aretz, Lucio Bertario
Publikováno v:
Gut, 59, 975-86
Gut, 59(7), 975-986
Recercat. Dipósit de la Recerca de Catalunya
instname
Gut, 59, 7, pp. 975-86
Dipòsit Digital de la UB
Universidad de Barcelona
Gut, 59(7), 975-986
Recercat. Dipósit de la Recerca de Catalunya
instname
Gut, 59, 7, pp. 975-86
Dipòsit Digital de la UB
Universidad de Barcelona
Item does not contain fulltext Peutz-Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic polyps throughout the gastrointestinal tract and mucocutaneous pigmentation. The majority of patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645f5d46147739a3d5e27a6e4e367f67
http://hdl.handle.net/2066/89762
http://hdl.handle.net/2066/89762
Autor:
Riccardo Fodde, A Brocker-Vriends, W. J. F. De Leeuw, Fred H. Menko, Hans F. A. Vasen, Hans Morreau, Dick Lindhout, G Moslein, S Vossen, Cees J. Cornelisse, Juul T. Wijnen, Pål Møller, Robert M. W. Hofstra, H. van der Klift, Astrid Stormorken, Rolf H. Sijmons, Hanne Meijers-Heijboer, Ying Wu, Carli M. J. Tops
Publikováno v:
Nature Genetics, 23, 142-144. Nature Publishing Group
Nature Genetics, 23(2), 142-144. Nature Publishing Group
Nature genetics, 23(2), 142-144. Nature Publishing Group
Nature Genetics, 23(2), 142-144. Nature Publishing Group
Nature genetics, 23(2), 142-144. Nature Publishing Group
Hereditary non-polyposis colorectal cancer (HNPCC) is a common autosomal dominant condition characterized by early onset colorectal cancer as well as other tumour types at different anatomical sites1. HNPCC tumours often display a high level of genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::febf990bbb40d58ad3016e62ffc9f430
https://doi.org/10.1038/13773
https://doi.org/10.1038/13773
Autor:
Julian R. Sampson, Yann Parc, Christoph Engel, Lucio Bertario, Mecklin Jp, Robin K. S. Phillips, M. P. de Leon, Heikki Järvinen, Peter Möller, Gabriel Capellá, Steffen Bülow, S. K. Clark, Ignacio Blanco, Shirley Hodgson, Juul T. Wijnen, Angel Alonso, H. J. W. Thomas, Stefan Aretz, Waltraut Friedl, Inge Bernstein, Astrid Stormorken, Hans F. A. Vasen, Fokko M. Nagengast, Frederik J. Hes, T. Myrhoi, Sabine Tejpar, Chrystelle Colas, John Burn, G Moslein, Ian M. Frayling, Laura Renkonen-Sinisalo
Publikováno v:
Gut, 57, 5, pp. 704-13
Recercat. Dipósit de la Recerca de Catalunya
instname
Gut, 57, 704-13
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Gut, 57, 704-13
Dipòsit Digital de la UB
Universidad de Barcelona
Item does not contain fulltext BACKGROUND: Familial adenomatous polyposis (FAP) is a well-described inherited syndrome, which is responsible for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cead46569a45c460451ee2c39a4bb94
https://hdl.handle.net/2066/70117
https://hdl.handle.net/2066/70117