"Cavestro, Giulia Martina" - Selaus tekijän mukaan TUNICRIS-julkaisut

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    • Delphi Initiative for Early-Onset Colorectal Cancer (DIRECt) International Management Guidelines 

      Cavestro, Giulia Martina; Mannucci, Alessandro; Balaguer, Francesc; Hampel, Heather; Kupfer, Sonia S; Repici, Alessandro; Sartore-Bianchi, Andrea; Seppälä, Toni T; Valentini, Vincenzo; Boland, Clement Richard; Brand, Randall E; Buffart, Tineke E; Burke, Carol A; Caccialanza, Riccardo; Cannizzaro, Renato; Cascinu, Stefano; Cercek, Andrea; Crosbie, Emma J; Danese, Silvio; Dekker, Evelien; Daca-Alvarez, Maria; Deni, Francesco; Dominguez-Valentin, Mev; Eng, Cathy; Goel, Ajay; Guillem, Josè G; Houwen, Britt B S L; Kahi, Charles; Kalady, Matthew F; Kastrinos, Fay; Kühn, Florian; Laghi, Luigi; Latchford, Andrew; Liska, David; Lynch, Patrick; Malesci, Alberto; Mauri, Gianluca; Meldolesi, Elisa; Møller, Pål; Monahan, Kevin J; Möslein, Gabriela; Murphy, Caitlin C; Nass, Karlijn; Ng, Kimmie; Oliani, Cristina; Papaleo, Enrico; Patel, Swati G; Puzzono, Marta; Remo, Andrea; Ricciardiello, Luigi (20.03.2022)
      article
      BACKGROUND & AIMS: Patients with early-onset colorectal cancer (eoCRC) are managed according to guidelines that are not age-specific. A multidisciplinary international group (DIRECt), composed of 69 experts, was convened ...

    • Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement 

      Møller, Pål; Seppälä, Toni T.; Ahadova, Aysel; Crosbie, Emma J.; Holinski-Feder, Elke; Scott, Rodney; Haupt, Saskia; Möslein, Gabriela; Winship, Ingrid; Broeke, Sanne W.Bajwa ten; Kohut, Kelly E.; Ryan, Neil; Bauerfeind, Peter; Thomas, Laura E.; Evans, D. Gareth; Aretz, Stefan; Sijmons, Rolf H.; Half, Elizabeth; Heinimann, Karl; Horisberger, Karoline; Monahan, Kevin; Engel, Christoph; Cavestro, Giulia Martina; Fruscio, Robert; Abu-Freha, Naim; Zohar, Levi; Laghi, Luigi; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Lino-Silva, Leonardo S.; Vaccaro, Carlos; Valle, Adriana Della; Rossi, Benedito Mauro; da Silva, Leandro Apolinário; de Oliveira Nascimento, Ivana Lucia; Rossi, Norma Teresa; Dębniak, Tadeusz; Mecklin, Jukka Pekka; Bernstein, Inge; Lindblom, Annika; Sunde, Lone; Nakken, Sigve; Heuveline, Vincent; Burn, John; Hovig, Eivind; Kloor, Matthias; Sampson, Julian R.; Dominguez-Valentin, Mev (10 / 2023)
      reviewarticle
      The recognition of dominantly inherited micro-satellite instable (MSI) cancers caused by pathogenic variants in one of the four mismatch repair (MMR) genes MSH2, MLH1, MSH6 and PMS2 has modified our understanding of ...

    • Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes 

      Møller, Pål; Haupt, Saskia; Ahadova, Aysel; Kloor, Matthias; Sampson, Julian R.; Sunde, Lone; Seppälä, Toni; Burn, John; Bernstein, Inge; Capella, Gabriel; Evans, D. Gareth; Lindblom, Annika; Winship, Ingrid; Macrae, Finlay; Katz, Lior; Laish, Ido; Vainer, Elez; Monahan, Kevin; Half, Elizabeth; Horisberger, Karoline; da Silva, Leandro Apolinário; Heuveline, Vincent; Therkildsen, Christina; Lautrup, Charlotte; Klarskov, Louise L.; Cavestro, Giulia Martina; Möslein, Gabriela; Hovig, Eivind; Dominguez-Valentin, Mev (2024)
      article
      Background: Colorectal cancers (CRCs) in the Lynch syndromes have been assumed to emerge through an accelerated adenoma-carcinoma pathway. In this model adenomas with deficient mismatch repair have an increased probability ...

    • Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database 

      Dominguez-Valentin, Mev; Haupt, Saskia; Seppälä, Toni T.; Sampson, Julian R.; Sunde, Lone; Bernstein, Inge; Jenkins, Mark A.; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capella, Gabriel; Balaguer, Francesc; Evans, Dafydd Gareth; Burn, John; Holinski-Feder, Elke; Bertario, Lucio; Bonanni, Bernardo; Lindblom, Annika; Levi, Zohar; Macrae, Finlay; Winship, Ingrid; Plazzer, John Paul; Sijmons, Rolf; Laghi, Luigi; Della Valle, Adriana; Heinimann, Karl; Dębniak, Tadeusz; Fruscio, Robert; Lopez-Koestner, Francisco; Alvarez-Valenzuela, Karin; Katz, Lior H.; Laish, Ido; Vainer, Elez; Vaccaro, Carlos; Carraro, Dirce Maria; Monahan, Kevin; Half, Elizabeth; Stakelum, Aine; Winter, Des; Kennelly, Rory; Gluck, Nathan; Sheth, Harsh; Abu-Freha, Naim; Greenblatt, Marc; Rossi, Benedito Mauro; Bohorquez, Mabel; Cavestro, Giulia Martina; Lino-Silva, Leonardo S.; Horisberger, Karoline; Tibiletti, Maria Grazia; Nascimento, Ivana do; Thomas, Huw; Rossi, Norma Teresa; Apolinário da Silva, Leandro; Zaránd, Attila; Ruiz-Bañobre, Juan; Heuveline, Vincent; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Renkonen-Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Therkildsen, Christina; Madsen, Mia Gebauer; Burgdorf, Stefan Kobbelgaard; Hopper, John L.; Win, Aung Ko; Haile, Robert W.; Lindor, Noralane; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane; Buchanan, Daniel D.; Thibodeau, Stephen N.; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schröck, Evelin; Steinke-Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Hüneburg, Robert; Redler, Silke; Büttner, Reinhard; Weitz, Jürgen; Pineda, Marta; Duenas, Nuria; Vidal, Joan Brunet; Moreira, Leticia; Sánchez, Ariadna; Hovig, Eivind; Nakken, Sigve; Green, Kate; Lalloo, Fiona; Hill, James; Crosbie, Emma; Mints, Miriam; Goldberg, Yael; Tjandra, Douglas; ten Broeke, Sanne W.; Kariv, Revital; Rosner, Guy; Advani, Suresh H.; Thomas, Lidiya; Shah, Pankaj; Shah, Mithun; Neffa, Florencia; Esperon, Patricia; Pavicic, Walter; Torrezan, Giovana Tardin; Bassaneze, Thiago; Martin, Claudia Alejandra; Moslein, Gabriela; Moller, Pål (03 / 2023)
      article
      Background: The Prospective Lynch Syndrome Database (PLSD) collates information on carriers of pathogenic or likely pathogenic MMR variants (path_MMR) who are receiving medical follow-up, including colonoscopy surveillance, ...

    • Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision 

      Zaffaroni, Gloria; Mannucci, Alessandro; Koskenvuo, Laura; de Lacy, Borja; Maffioli, Anna; Bisseling, Tanya; Half, Elizabeth; Cavestro, Giulia Martina; Valle, Laura; Ryan, Neil; Aretz, Stefan; Brown, Karen; Buttitta, Francesco; Carneiro, Fatima; Claber, Oonagh; Blanco-Colino, Ruth; Collard, Maxime; Crosbie, Emma; Cunha, Miguel; Doulias, Triantafyllos; Fleming, Christina; Heinrich, Henriette; Hüneburg, Robert; Metras, Julie; Nagtegaal, Iris; Negoi, Ionut; Nielsen, Maartje; Pellino, Gianluca; Ricciardiello, Luigi; Sagir, Abdurrahman; Sánchez-Guillén, Luis; Seppälä, Toni T.; Siersema, Peter; Striebeck, Benedikt; Sampson, Julian R.; Latchford, Andrew; Parc, Yann; Burn, John; Möslein, Gabriela (03.05.2024)
      article
      BACKGROUND: Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of colorectal and other cancers. METHODS: A team ...