Browsing by Author Navarro, Matilde
Showing results 18 to 31 of 31
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| Issue Date | Title | Author(s) |
|---|---|---|
| 28-Jun-2021 | No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study | Dominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål |
| 21-Jun-2019 | NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas | Belhadj, Sami; Quintana, Isabel; Mur, Pilar; Munoz-Torres, Pau M.; Alonso Aguado, Maria Henar; Navarro, Matilde; Terradas, Mariona; Pinol, Virginia; Brunet, Joan; Moreno Aguado, Víctor; Lázaro García, Conxi; Capellá, G. (Gabriel); Valle Velasco, Laura |
| Nov-2004 | Organochlorine exposure and colorectal cancer risk | Howsam, Mike; Grimalt, Joan O.; Guinó, Elisabet; Navarro, Matilde; Martí Ragué, Joan; Peinado Morales, Miguel Á. (Miguel Ángel); Capellá, G. (Gabriel); Moreno Aguado, Víctor; Bellvitge Colorectal Cancer Group |
| 17-Jan-2012 | Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers | Lázaro García, Conxi; Blanco Guillermo, Ignacio; Tornero, Eva; Navarro, Matilde; CIMBA Consortium |
| 3-Jun-2004 | Oxaliplatin, Fluorouracil, and Leucovorin as Adjuvant Treatment for Colon Cancer | André, Thierry; Boni, Corrado; Mounedji-Boudiaf, Lamia; Navarro, Matilde; Tabernero Caturla, Josep; Hickish, Tamas; Topham, Clare; Zaninelli, Marta; Clingan, Philip; Bridgewater, John; Tabah-Fisch, Isabelle; Gramont, Aimery de; Adjuvant Treatment of Colon Cancer (MOSAIC) Investigators |
| 19-Jul-2004 | Polymorphisms in prostaglandin synthase 2/cyclooxygenase 2 (PTGS2/COX2) and risk of colorectal cancer | Cox, David G.; Pontes García, Caridad; Guinó, Elisabet; Navarro, Matilde; Osorio, Ana; Canzian, Federico; Moreno Aguado, Víctor; Bellvitge Colorectal Cancer Study Group |
| Oct-2018 | Primary constitutional MLH1 epimutations: a focal epigenetic event | Dámaso, Estela; Castillejo, Adela; Arias, María del Mar; Canet Hermida, Júlia; Navarro, Matilde; Valle Domínguez, Jesús del; Campos, Olga; Fernández, Anna; Marín, Fátima; Turchetti, Daniela; García Díaz, Juan de Dios; Lázaro García, Conxi; Genuardi, Maurizio; Rueda, Daniel; Alonso, Ángel; Soto, Jose Luis; Hitchins, Megan; Pineda Riu, Marta; Capellá, G. (Gabriel) |
| 1-Jul-2020 | Risk-reducing gynecological surgery in Lynch syndrome: results of an international survey from the prospective Lynch syndrome database | Dominguez Valentin, Mev; Seppälä, Toni T.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Gonzalez, María Laura; Kalfayan, Pablo; Sampson, Julian R.; Ryan, Neil A. J.; Evans, D. Gareth; Møller, Pål; Crosbie, Emma J. |
| 1-Dec-2020 | Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report. | Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; González, María Laura; Kalfayan, Pablo; Ryan, Neil A. J.; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Auranen, Annika; Hopper, John L.; Ko Win, Aung; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppälä, Toni T.; Møller, Pål |
| 14-Aug-2020 | Role of POLE and POLD1 in familial cancer | Mur, Pilar; García Mulero, Sandra; Valle, Jesús del; Magraner Pardo, Lorena; Vidal-Bel, August; Pineda Riu, Marta; Cinnirella, Giacomo; Martín Ramos, Edgar; Pons, Tirso; López Dóriga Guerra, Adriana; Belhadj, Sami; Feliubadaló i Elorza, Maria Lídia; Muñoz Torres, Pau M.; Navarro, Matilde; Grau Garcés, Èlia; Darder, Esther; Llort, Gemma; Sanz, Judit; Ramón y Cajal, Teresa; Balmaña, Judith; Brunet, Joan; Moreno Aguado, Víctor; Piulats, Josep M.; Matias-Guiu, Xavier; Sanz Pamplona, Rebeca; Aligué i Alemany, Rosa Maria; Capellá, G. (Gabriel); Lázaro García, Conxi; Valle, Laura |
| 8-Feb-2016 | Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis | Mur, Pilar; Sánchez Cuartielles, Elena; Aussó, Susanna; Aiza, Gemma; Valdés Mas, Rafael; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Urioste, Miguel; Lázaro García, Conxi; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Puente, Xose S.; Valle Velasco, Laura |
| 2005 | Sex differences in hospital readmission among colorectal cancer patients. | González Ruiz, Juan Ramón; Fernández Muñoz, Esteve; Moreno Aguado, Víctor; Ribes Puig, Josepa; Peris, Mercè; Navarro, Matilde; Cambray i Amenós, Maria; Borràs Andrés, Josep Maria |
| 14-Oct-2019 | Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report | Dominguez Valentin, Mev; Seppälä, Toni T.; Sampson, Julian R.; Macrae, Finlay; Winship, Ingrid; Evans, D. Gareth; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Pylvanainen, Kirsi; Renkonen Sinisalo, Laura; Lepisto, Anna; Lindblom, Annika; Plazzer, John-Paul; Tjandra, Douglas; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Ronlund, Karina; Nielsen, Randi Thyregaard; Yilmaz, Mette; Elvang, Louise Laurberg; Katz, Lior; Nielsen, Maartje; ten Broeke, Sanne W.; Nakken, Sigve; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Knebel Doeberitz, Magnus v; Ahadova, Aysel; Lindor, Noralane; Steinke Lange, Verena; Holinski Feder, Elke; Mecklin, Jukka-Pekka; Møller, Pål |
| 17-Apr-2013 | Telomere length and genetic anticipation in lynch syndrome | Seguí Gracia, Nuria; Pineda Riu, Marta; Guinó, Elisabet; Borràs Flores, Ester; Navarro, Matilde; Bellido Molías, Fernando; Moreno Aguado, Víctor; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Valle Velasco, Laura |