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المؤلفون: Seçil Aksoy, Michael O. Woods, Heinric Williams, Bruno Buecher, Finlay A. Macrae, Lotte N. Krogh, Jay Qiu, Wan K.W. Juhari, Jan T. Lowery, Anne-Marie Gerdes, Magnus von Knebel Doeberitz, Luigi Ricciardiello, Karsten Schulmann, Jose Luis Soto, Kristina Lagerstedt-Robinson, Kiwamu Akagi, Raj Ramesar, Uffe Birk Jensen, Angel Alonso, Robert Hüneburg, Olivier Caron, Michel Longy, Jan Lubinski, Kate Green, Annabel Goodwin, D. Gareth Evans, Julie Wods, Leigha Senter, Matthew F. Kalady, Mark Clendenning, Barbara A. Leggett, Ravindran Ankathil, Swati G. Patel, Julian Barwell, Katherine M. Tucker, Grant Lee, Pascaline Berthet, Dawn M. Nixon, Sonia S. Kupfer, Naohiro Tomita, Susan Parry, Trinidad Caldés, Robert W. Haile, Edenir Inêz Palmero, Karin Alvarez, Cassandra B. Nichols, Mark A. Jenkins, N. Jewel Samadder, Loic LeMarchand, John Burn, Francisco Lopez, Rodney J. Scott, Pierre Laurent-Puig, Julie Arnold, Christina Therkildsen, Hans K. Schackert, Pilar Garre, Reinhard Buettner, Adriana Della Valle, Patricia Esperon, Wolff Schmiegel, Karl Heinimann, Inge Bernstein, Matthias Kloor, Nicoline Hoogerbrugge, Rui Manuel Reis, Fränzel J.B. Van Duijnhoven, Christoph Engel, Mohd Nizam Zahary, Sylviane Olschwang, Sapna Syngal, Valérie Bonadona, Nicholas Pachter, Matilde Navarro, Albert de la Chapelle, Beate Betz, Jukka-Pekka Mecklin, Catherine Noguès, Elena M. Stoffel, Toni T. Seppälä, Chrystelle Colas, Anneke Lucassen, Allan D. Spigelman, Youenn Drouet, Elisa J. Cops, Uri Ladabaum, Steve Thibodeau, Jeffrey N. Weitzel, Fiona Lalloo, Patrick J. Morrison, Maurizio Genuardi, Kohji Tanakaya, Patrick M. Lynch, Frederik J. Hes, William D. Foulkes, Carmen Guillén-Ponce, Jenny von Salomé, Emilia Rogoża-Janiszewska, Andrew Latchford, John L. Hopper, Carrie Snyder, Verónica Barca-Tierno, Gabriela Möslein, Lauren M. Gima, Melissa C. Southey, Paul A. James, Marion Dhooge, Claudia Perne, Steven Gallinger, Heather Hampel, Amanda B. Spurdle, Ingrid Winship, Emmanuelle Fourme, Rish K. Pai, Daniela Turchetti, Marta Pineda, Jürgen Weitz, James Hill, Daniel D. Buchanan, Carlos A. Vaccaro, Noralane M. Lindor, Rachel Pearlman, Pål Møller, Christian P. Strassburg, Jane C. Figueiredo, Aída Falcón de Vargas, Silke Zachariae, Karolin Bucksch, Joanne Ngeow, Silke Redler, Henrik Okkels, Maija R.J. Kohonen-Corish, Hans F. A. Vasen, Verena Steinke-Lange, Roselyne Guimbaud, Deepak Vangala, Isabelle Coupier, Nils Rahner, Berrin Tunca, Sanne W. Bajwa-ten Broeke, Niels de Wind, Sophie Lejeune, José Gaston Guillem, Karin Wadt, Polly A. Newcomb, Elke Holinski-Feder, Florencia Neffa, Rodrigo Santa Cruz Guindalini, Paul E. Wise, Julian R. Sampson, Graham Casey, Lene Juel Rasmussen, Rolf H. Sijmons, Tadeusz Dębniak, Ann-Sofie Backman, Joji Utsunomiya, Melyssa Aronson, Aung Ko Win, Yves-Jean Bignon, Judy W. C. Ho, Robyn L. Ward, Mev Dominguez-Valentin, Karolina Malińska, Elizabeth E. Half, John-Paul Plazzer, Marjolijn J. L. Ligtenberg, Rachel Austin, Nicola K. Poplawski, Marcia Cruz-Correa, Nagahide Matsubara, Charlotte Kvist Lautrup, Thomas Hansen, Tatsuro Yamaguchi, Thomas John, David J. Amor, Ilana Solomon, Yun-Hee Choi, Meghan J. van Wanzeele, Rakefet Shtoyerman, Vanessa Huntley, Maartje Nielsen, Deborah Neklason, Kevin J. Monahan, Gülçin Tezcan, Stefan Aretz, Talya Boisjoli, Sophie Giraud, Thierry Frebourg, Christophe Rosty, Heike Görgens, Lone Sunde, Allyson Templeton, Jacob Nattermann, Mala Pande, Joan Brunet, Nancy Uhrhammer, James M. Church, Florencia Spirandelli, Laurent Briollais, James G. Dowty, Jeanette C. Reece, Rachel Susman, Fay Kastrinos, Kirsi Pylvänäinen, Gabriel Capellá, Helène Schuster, Min H. Chew, Markus Loeffler, Christine Lasset, Michael J. Hall, Capuccine Delnatte, Floor A. Duijkers
المساهمون: Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA), Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP), UNICANCER, Digital Precision Cancer Medicine (iCAN), ATG - Applied Tumor Genomics, HUS Abdominal Center, Clinical sciences, Medical Genetics, Win A.K., Dowty J.G., Reece J.C., Lee G., Templeton A.S., Plazzer J.-P., Buchanan D.D., Akagi K., Aksoy S., Alonso A., Alvarez K., Amor D.J., Ankathil R., Aretz S., Arnold J.L., Aronson M., Austin R., Backman A.-S., Bajwa-ten Broeke S.W., Barca-Tierno V., Barwell J., Bernstein I., Berthet P., Betz B., Bignon Y.-J., Boisjoli T., Bonadona V., Briollais L., Brunet J., Bucksch K., Buecher B., Buettner R., Burn J., Caldes T., Capella G., Caron O., Casey G., Chew M.H., Choi Y.-H., Church J., Clendenning M., Colas C., Cops E.J., Coupier I., Cruz-Correa M., de la Chapelle A., de Wind N., Debniak T., Della Valle A., Delnatte C., Dhooge M., Dominguez-Valentin M., Drouet Y., Duijkers F.A., Engel C., Esperon P., Evans D.G., Falcon de Vargas A., Figueiredo J.C., Foulkes W., Fourme E., Frebourg T., Gallinger S., Garre P., Genuardi M., Gerdes A.-M., Gima L.M., Giraud S., Goodwin A., Gorgens H., Green K., Guillem J., Guillen-Ponce C., Guimbaud R., Guindalini R.S.C., Half E.E., Hall M.J., Hampel H., Hansen T.V.O., Heinimann K., Hes F.J., Hill J., Ho J.W.C., Holinski-Feder E., Hoogerbrugge N., Huneburg R., Huntley V., James P.A., Jensen U.B., John T., Juhari W.K.W., Kalady M., Kastrinos F., Kloor M., Kohonen-Corish M.R., Krogh L.N., Kupfer S.S., Ladabaum U., Lagerstedt-Robinson K., Lalloo F., Lasset C., Latchford A., Laurent-Puig P., Lautrup C.K., Leggett B.A., Lejeune S., LeMarchand L., Ligtenberg M., Lindor N., Loeffler M., Longy M., Lopez F., Lowery J., Lubinski J., Lucassen A.M., Lynch P.M., Malinska K., Matsubara N., Mecklin J.-P., Moller P., Monahan K., Morrison P.J., Nattermann J., Navarro M., Neffa F., Neklason D., Newcomb P.A., Ngeow J., Nichols C., Nielsen M., Nixon D.M., Nogues C., Okkels H., Olschwang S., Pachter N., Pai R.K., Palmero E.I., Pande M., Parry S., Patel S.G., Pearlman R., Perne C., Pineda M., Poplawski N.K., Pylvanainen K., Qiu J., Rahner N., Ramesar R., Rasmussen L.J., Redler S., Reis R.M., Ricciardiello L., Rogoza-Janiszewska E., Rosty C., Samadder N.J., Sampson J.R., Schackert H.K., Schmiegel W., Schulmann K., Schuster H., Scott R., Senter L., Seppala T.T., Shtoyerman R., Sijmons R.H., Snyder C., Solomon I.B., Soto J.L., Southey M.C., Spigelman A., Spirandelli F., Spurdle A.B., Steinke-Lange V., Stoffel E.M., Strassburg C.P., Sunde L., Susman R., Syngal S., Tanakaya K., Tezcan G., Therkildsen C., Thibodeau S., Tomita N., Tucker K.M., Tunca B., Turchetti D., Uhrhammer N., Utsunomiya J., Vaccaro C., van Duijnhoven F.J.B., van Wanzeele M.J., Vangala D.B., Vasen H.F.A., von Knebel Doeberitz M., von Salome J., Wadt K.A.W., Ward R.L., Weitz J., Weitzel J.N., Williams H., Winship I., Wise P.E., Wods J., Woods M.O., Yamaguchi T., Zachariae S., Zahary M.N., Hopper J.L., Haile R.W., Macrae F.A., Moslein G., Jenkins M.A.
المصدر: The Lancet Oncology, 22(7), 1014-1022. ELSEVIER SCIENCE INC
International Mismatch Repair Consortium, Sunde, L E M, Lautrup, C K, Okkels, H & Bernstein, I 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome : a retrospective cohort study ', The Lancet. Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
The International Mismatch Repair Consortium 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study ', The Lancet Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
Lancet Oncology
Lancet Oncology, Elsevier, 2021, 22 (7), pp.1014-1022. ⟨10.1016/S1470-2045(21)00189-3⟩
The International Mismatch Repair Consortium 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome : a retrospective cohort study ', The Lancet Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
Lancet Oncology, 22, 7, pp. 1014-1022
Lancet Oncology, 22, 1014-1022مصطلحات موضوعية: 0301 basic medicine, Proband, Oncology, Male, Heredity, DNA mismatch repair, [SDV]Life Sciences [q-bio], SUSCEPTIBILITY, Settore MED/03 - GENETICA MEDICA, 0302 clinical medicine, Residence Characteristics, Risk Factors, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], PMS2, ComputingMilieux_MISCELLANEOUS, MLH1, Age Factors, Middle Aged, Penetrance, Lynch syndrome, 3. Good health, Pedigree, Phenotype, 030220 oncology & carcinogenesis, Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis, Female, Adult, medicine.medical_specialty, PENETRANCE, congenital, hereditary, and neonatal diseases and abnormalities, GENES, 3122 Cancers, colorectal cancer, BREAST, Risk Assessment, 03 medical and health sciences, Sex Factors, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Retrospective Studies, business.industry, MUTATIONS, Cancer, medicine.disease, digestive system diseases, MSH2, MSH6, MODEL, INDIVIDUALS, 030104 developmental biology, Lynch Syndrome, Gene-Environment Interaction, business
وصف الملف: application/pdf; STAMPA
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المؤلفون: Michael Hoffmeister, Gabriel Capellá, Finlay A. Macrae, John Burn, Rodney J. Scott, Hendrik Bläker, Christoph Engel, Gabriela Möslein, Robert Hüneburg, Hermann Brenner, Maartje Nielsen, Magnus von Knebel Doeberitz, Jacob Nattermann, Sanne W. ten Broeke, Verena Steinke-Lange, Luigi Laghi, Toni T. Seppälä, Jukka-Pekka Mecklin, Richard Gallon, Julian R. Sampson, Elke Holinski-Feder, Aysel Ahadova, Pål Møller, Matthias Kloor, Mev Dominguez-Valentin, Hans F. A. Vasen
المساهمون: HUS Abdominal Center, Clinicum, Department of Biochemistry and Developmental Biology, Department of Surgery, Helsinki University Hospital Area, Faculty of Medicine, University of Helsinki
المصدر: Dipòsit Digital de la UB
Universidad de Barcelona
International Journal of Cancer, 148(4), 800-811. WILEYمصطلحات موضوعية: Cancer Research, Colorectal cancer, medicine.medical_treatment, Colonoscopy, DNA Mismatch Repair, ADENOMA DETECTION, 0302 clinical medicine, Risk Factors, Epidemiology, Mass Screening, Prospective cohort study, MUTATION, RISK, medicine.diagnostic_test, incident cancer risk, TUMORS, Lynch syndrome, 3. Good health, Oncology, 030220 oncology & carcinogenesis, Population Surveillance, syöpätaudit, Colorectal Neoplasms, koloskopia, medicine.medical_specialty, LONG-TERM, 3122 Cancers, colorectal cancer, suolistosyövät, INTERVAL CANCERS, 03 medical and health sciences, INTESTINAL MICROBIOTA, Càncer colorectal, COLON, medicine, MANAGEMENT, Humans, Lynchin oireyhtymä, Intensive care medicine, paksusuolisyöpä, perinnölliset taudit, seulontatutkimus, business.industry, mismatch repair deficiency, Microsatellite instability, Cancer, Colonoscòpia, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Polypectomy, digestive system diseases, DNA Repair Enzymes, microsatellite instability, business, colonoscopy surveillance
وصف الملف: application/pdf; fulltext
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المؤلفون: Reinhard Büttner, Päivi Peltomäki, Monique E. van Leerdam, Alexandra M. J. Langers, Markus Loeffler, Wouter T. de Vos tot Nederveen Cappel, Robert Hüneburg, Christoph Engel, Deepak Vangala, Stefan Aretz, Christian P. Strassburg, Laura Renkonen-Sinisalo, Albrecht Stenzinger, Volker Endris, Paul C. van de Meeberg, Maarten A J M Jacobs, Toni T. Seppälä, Hendrik Bläker, Anna Lepistö, Aysel Ahadova, Elke Holinski-Feder, Nils Rahner, Jukka-Pekka Mecklin, Monika Morak, Mariëtte C.A. van Kouwen, Matthias Kloor, Verena Steinke-Lange, Magnus von Knebel Doeberitz, Marie Louise Verhulst, Karolin Bucksch, Gabriela Möslein, Jürgen Weitz, Hans F. A. Vasen, Stefanie Holzapfel, Jan J. Koornstra, Silke Zachariae, Marloes Bigirwamungu-Bargeman, Karsten Schulmann, Kirsi Pylvänäinen, Juda Vecht
المساهمون: HUS Abdominal Center, Clinicum, University of Helsinki, II kirurgian klinikka, Department of Surgery, Research Programs Unit, ATG - Applied Tumor Genomics, Gastroenterology and hepatology
المصدر: Engel, C, Ahadova, A, Seppälä, T T, Aretz, S, Bigirwamungu-Bargeman, M, Bläker, H, Bucksch, K, Büttner, R, de Vos tot Nederveen Cappel, W T, Endris, V, Holinski-Feder, E, Holzapfel, S, Hüneburg, R, Jacobs, M A J M, Koornstra, J J, Langers, A M, Lepistö, A, Morak, M, Möslein, G, Peltomäki, P, Pylvänäinen, K, Rahner, N, Renkonen-Sinisalo, L, Schulmann, K, Steinke-Lange, V, Stenzinger, A, Strassburg, C P, van de Meeberg, P C, van Kouwen, M, van Leerdam, M, Vangala, D B, Vecht, J, Verhulst, M L, von Knebel Doeberitz, M, Weitz, J, Zachariae, S, Loeffler, M, Mecklin, J P, Kloor, M, Vasen, H F, German HNPCC Consortium, the Dutch Lynch Syndrome Collaborative Group & Finnish Lynch Syndrome Registry 2020, ' Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome ', Gastroenterology, vol. 158, no. 5, pp. 1326-1333 . https://doi.org/10.1053/j.gastro.2019.12.032
Gastroenterology, 158(5), 1326-1333. W B SAUNDERS CO-ELSEVIER INC
Gastroenterology, 158, 5, pp. 1326-1333
Gastroenterology, 158, 1326-1333
Gastroenterology, 158(5), 1326-1333. W.B. Saunders Ltdمصطلحات موضوعية: 0301 basic medicine, Oncology, Male, Colorectal cancer, DNA Mutational Analysis, genetic analysis, HEREDITARY, cancer risk, GUIDELINES, DNA Mismatch Repair, 0302 clinical medicine, Germany, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Prospective Studies, prognostic factor, Finland, beta Catenin, Netherlands, Outcome, Prognostic Factor, Gastroenterology, Genetic Analysis, Colonoscopy, Middle Aged, CANCER, Lynch syndrome, Cancer Risk, 3. Good health, DNA-Binding Proteins, DEFICIENCY, MutS Homolog 2 Protein, syöpägeenit, outcome, 030211 gastroenterology & hepatology, DNA mismatch repair, Female, MutL Protein Homolog 1, geenitutkimus, Adenoma, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, 3122 Cancers, Adenomatous Polyposis Coli Protein, INSTABILITY, SOCIETY, MLH1, 03 medical and health sciences, Internal medicine, medicine, MANAGEMENT, Humans, Lynchin oireyhtymä, neoplasms, paksusuolisyöpä, Hepatology, business.industry, Cancer, nutritional and metabolic diseases, ennusteet, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH6, 030104 developmental biology, MSH2, Mutation, business
وصف الملف: application/pdf; fulltext