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The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome
Crosbie, Emma J., Ryan, Neil A. J., Arends, Mark J., Bosse, Tjalling, Burn, John, Cornes, Joanna M., Crawford, Robin, Eccles, Diana, Frayling, Ian M., Ghaem-Maghami, Sadaf, Hampel, Heather, Kauff, Noah D., Kitchener, Henry C., Kitson, Sarah J., Manchanda, Ranjit, McMahon, Raymond F. T., Monahan, Kevin J., Menon, Usha, Møller, Pål, Möslein, Gabriela, Rosenthal, Adam, Sasieni, Peter, Seif, Mourad W., Singh, Naveena, Skarrott, Pauline, Snowsill, Tristan M., Steele, Robert, Tischkowitz, Marc, Evans, D. Gareth
Published in Genetics in medicine (01.10.2019)
Published in Genetics in medicine (01.10.2019)
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Journal Article
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Møller, Pål, Seppälä, Toni T, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paulo, Gareth Evans, D, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf H, Jeffries, Jacqueline, Vasen, Hans F A, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H, Hill, James, Wijnen, Juul T, Jenkins, Mark A, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Renkonen-Sinisalo, Laura, Valentin, Mev Dominguez, Frayling, Ian M, Plazzer, John-Paul, Pylvanainen, Kirsi, Genuardi, Maurizio, Mecklin, Jukka-Pekka, Moeslein, Gabriela, Sampson, Julian R, Capella, Gabriel
Published in Gut (01.07.2018)
Published in Gut (01.07.2018)
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Journal Article
Comprehensive characterisation of Lynch syndrome and screening strategies: a cohort study of individuals at risk from Latin American genetic registries
Rossi, Benedito Mauro, Bohorquez, Mabel, Spirandelli, Florencia, Møller, Pål, Balavarca, Yesilda, Dominguez-Valentin, Mev
Published in The lancet oncology (01.07.2022)
Published in The lancet oncology (01.07.2022)
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Journal Article
Response to Tolva et al
Sampson, Julian R., Dominguez-Valentin, Mev, Seppälä, Toni T., Møller, Pål
Published in Genetics in medicine (01.04.2020)
Published in Genetics in medicine (01.04.2020)
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Journal Article
Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers
Kim, Shana J., Lubinski, Jan, Huzarski, Tomasz, Møller, Pål, Armel, Susan, Karlan, Beth Y., Senter, Leigha, Eisen, Andrea, Foulkes, William D., Singer, Christian F., Tung, Nadine, Bordeleau, Louise, Neuhausen, Susan L., Olopade, Olufunmilayo I., Eng, Charis, Weitzel, Jeffrey N., Fruscio, Robert, Narod, Steven A., Kotsopoulos, Joanne
Published in Cancer epidemiology, biomarkers & prevention (01.11.2021)
Published in Cancer epidemiology, biomarkers & prevention (01.11.2021)
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Journal Article
Correction to: Letter to the Editor—Recent advances in Lynch syndrome
Møller, Pål, Sampson, Julian, Dominguez-Valentin, Mev, Burn, John, Sunde, Lone, Möslein, Gabriela, Mecklin, Jukka-Pekka, Seppälä, Toni
Published in Familial cancer (01.04.2021)
Published in Familial cancer (01.04.2021)
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Journal Article
Letter to the Editor-Recent advances in Lynch syndrome
Møller, Pål, Sampson, Julian, Dominguez-Valentin, Mev, Burn, John, Sunde, Lone, Möslein, Gabriela, Mecklin, Jukka-Pekka, Seppälä, Toni
Published in Familial cancer (01.04.2021)
Published in Familial cancer (01.04.2021)
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Journal Article
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
Seppälä, Toni, Pylvänäinen, Kirsi, Evans, Dafydd Gareth, Järvinen, Heikki, Renkonen-Sinisalo, Laura, Bernstein, Inge, Holinski-Feder, Elke, Sala, Paola, Lindblom, Annika, Macrae, Finlay, Blanco, Ignacio, Sijmons, Rolf, Jeffries, Jacqueline, Vasen, Hans, Burn, John, Nakken, Sigve, Hovig, Eivind, Rødland, Einar Andreas, Tharmaratnam, Kukatharmini, de Vos tot Nederveen Cappel, Wouter H., Hill, James, Wijnen, Juul, Jenkins, Mark, Genuardi, Maurizio, Green, Kate, Lalloo, Fiona, Sunde, Lone, Mints, Miriam, Bertario, Lucio, Pineda, Marta, Navarro, Matilde, Morak, Monika, Frayling, Ian M., Plazzer, John-Paul, Sampson, Julian R., Capella, Gabriel, Möslein, Gabriela, Mecklin, Jukka-Pekka, Møller, Pål
Published in Hereditary cancer in clinical practice (10.10.2017)
Published in Hereditary cancer in clinical practice (10.10.2017)
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Journal Article
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Vasen, Hans F A, Blanco, Ignacio, Aktan-Collan, Katja, Gopie, Jessica P, Alonso, Angel, Aretz, Stefan, Bernstein, Inge, Bertario, Lucio, Burn, John, Capella, Gabriel, Colas, Chrystelle, Engel, Christoph, Frayling, Ian M, Genuardi, Maurizio, Heinimann, Karl, Hes, Frederik J, Hodgson, Shirley V, Karagiannis, John A, Lalloo, Fiona, Lindblom, Annika, Mecklin, Jukka-Pekka, Møller, Pal, Myrhoj, Torben, Nagengast, Fokko M, Parc, Yann, Ponz de Leon, Maurizio, Renkonen-Sinisalo, Laura, Sampson, Julian R, Stormorken, Astrid, Sijmons, Rolf H, Tejpar, Sabine, Thomas, Huw J W, Rahner, Nils, Wijnen, Juul T, Järvinen, Heikki Juhani, Möslein, Gabriela
Published in Gut (01.06.2013)
Published in Gut (01.06.2013)
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Journal Article
Predictors of Contralateral Prophylactic Mastectomy in Women With a BRCA1 or BRCA2 Mutation: The Hereditary Breast Cancer Clinical Study Group
METCAIFE, Kelly A, LUBINSKI, Jan, TUNG, Nadine, GRONWALD, Jacek, CUMMINGS, Shelly, WAGNER, Teresa, MANOUKIAN, Siranoush, MØLLER, Pal, WEITZEL, Jeffrey, PING SUN, NAROD, Steven A, GHADIRIAN, Parviz, LYNCH, Henry, KIM-SING, Charmaine, FRIEDMAN, Eitan, FOULKES, William D, DOMCHEK, Susan, AINSWORTH, Peter, ISAACS, Claudine
Published in Journal of clinical oncology (01.03.2008)
Published in Journal of clinical oncology (01.03.2008)
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Journal Article
Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate Cancer
Grindedal, Eli Marie, Møller, Pål, Eeles, Ros, Stormorken, Astrid Tenden, Bowitz-Lothe, Inger Marie, Landrø, Stefan Magnus, Clark, Neal, Kvåle, Rune, Shanley, Susan, Mæhle, Lovise
Published in Cancer epidemiology, biomarkers & prevention (01.09.2009)
Published in Cancer epidemiology, biomarkers & prevention (01.09.2009)
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Journal Article
Genetic epidemiology of BRCA mutations – family history detects less than 50% of the mutation carriers
Møller, Pål, Hagen, Anne Irene, Apold, Jaran, Maehle, Lovise, Clark, Neal, Fiane, Bent, Løvslett, Kjell, Hovig, Eivind, Vabø, Anita
Published in European journal of cancer (1990) (01.07.2007)
Published in European journal of cancer (1990) (01.07.2007)
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Journal Article
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations
Geirdal, Amy Østertun, Reichelt, Jon G., Dahl, Alv A., Heimdal, Ketil, Mæhle, Lovise, Stormorken, Astrid, Møller, Pål
Published in Familial cancer (01.06.2005)
Published in Familial cancer (01.06.2005)
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Journal Article
MSH2 genomic deletions are a frequent cause of HNPCC
Wijnen, Juul, van der Klift, Heleen, Vasen, Hans, Khan, P. Meera, Menko, Fred, Tops, Carli, Meijers Heijboer, Hanne, Lindhout, Dick, Møller, Pål, Fodde, Ricardo
Published in Nature genetics (01.12.1998)
Published in Nature genetics (01.12.1998)
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Journal Article