Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Ignacio Blanco"'
Autor:
Jean-Marc Grégoire, Athmane Bouroubi, Roxane Beauchamp, Arnaud Bocquet, Anne-Marie Schmitt, Marlene Guiraud, Pierre Wolkenstein, Ignacio Blanco, Isabelle Rauly-Lestienne
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Neurofibromatosis type 1 is an inherited condition with variable phenotypic expression and a high medical and social burden. The objectives of this patient survey were to better understand the real-world experiences of patients living with
Autor:
Ferran, Vilaplana, Andrea, Ros, Belen, Garcia, Ignacio, Blanco, Elisabeth, Castellanos, Nicholas John, Edwards, Xavier, Valldeperas, Susana, Ruiz-Bilbao, Antonio, Sabala
Publikováno v:
Ophthalmic genetics. 42(4)
To describe the clinical characteristics, the imaging findings, and the genetic results of a patient with cone-rod dystrophy (CORD) related to mutations inA case report of atypicalA 57-year-old female who had reported a visual loss for 5 years. BCVA
Autor:
Nuria Izquierdo-Useros, Carolina González-Fernández, Victor Urrea, Joaquim Segalés, Victor Guallar, Jaume Trapé, Roger Paredes, Jorge Carrillo, Julià Blanco, Jordi Rodon, Júlia Vergara-Alert, Rafel Perez-Vidal, Antonia Flor, Benjamin Trinité, Rosalba Lepore, Gloria Trujillo, Ferran Tarrés-Freixas, Ignacio Blanco, Bonaventura Clotet, Ruth Toledo, Eulalia Grau, Edwards Pradenas, Anna Chamorro, Carla Rovirosa, Marta Massanella, Raquel Ortiz, Silvia Marfil
Publikováno v:
IRTA Pubpro. Open Digital Archive
Institut de Recerca i Tecnologia Agroalimentàries (IRTA)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Viruses
Volume 13
Issue 6
Viruses, Vol 13, Iss 1135, p 1135 (2021)
VIRUSES-BASEL
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Institut de Recerca i Tecnologia Agroalimentàries (IRTA)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Viruses
Volume 13
Issue 6
Viruses, Vol 13, Iss 1135, p 1135 (2021)
VIRUSES-BASEL
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Altres ajuts: This work was partially funded by Grifols, the Departament de Salut of the Generalitat de Catalunya (grant SLD016 to J.B. and Grant SLD015 to J.C.), and the crowdfunding initiatives #joemcorono, BonPreu/Esclat and Correos. With the spre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81cbc50c4d054b4957bcd12cdd2b2b7
https://doi.org/10.3390/v13061135
https://doi.org/10.3390/v13061135
Autor:
Gabriel Capellá, Patricia Esperon, Christoph Engel, Rolf H. Sijmons, María Laura Gonzalez, Matilde Navarro, Francisco López-Köstner, Julian R. Sampson, Miquel Serra-Burriel, Karin Alvarez, Ingrid Winship, Nathan Gluck, Lone Sunde, Reinhard Büttner, Giulia Martina Cavestro, Wouter H. de Vos tot Nederveen Cappel, Jukka-Pekka Mecklin, Marc S. Greenblatt, Kate Green, Robert Hüneburg, Markus Loeffler, Maria Grazia Tibiletti, Tamara Alejandra Piñero, Florencia Neffa, Lucio Bertario, Ariadna Sánchez, Verena Steinke-Lange, Christina Therkildsen, Jane C. Figueiredo, Douglas Tjandra, Magnus von Knebel Doeberitz, Lior H. Katz, Steven Gallinger, Noralane M. Lindor, Gabriela Möslein, Adriana Della Valle, John L. Hopper, Einar Andreas Rødland, Miriam Mints, Annika Lindblom, Ian M. Frayling, Polly A. Newcomb, Pål Møller, Sanne W. ten Broeke, Laura Renkonen-Sinisalo, Sigve Nakken, Stefanie Holzapfel, Finlay A. Macrae, Stefan Aretz, Nils Rahner, Karin Wadt, Robert W. Haile, Francesc Balaguer, Revital Kariv, Stephen N. Thibodeau, Huw D. Thomas, Emma J Crosbie, Deepak Vangala, Monika Morak, Ignacio Blanco, Hans K. Schackert, Henrik Okkels, Mev Dominguez-Valentin, Oliver G. Denton, John-Paul Plazzer, Zohreh Ketabi, James Hill, Loic Le Marchand, Mark A. Jenkins, Inge Bernstein, D. Gareth Evans, Heike Görgens, Marta Pineda, John Burn, Kirsi Pylvänäinen, Eivind Hovig, Hans F. A. Vasen, Pablo Kalfayan, Toni T. Seppälä, Aung Ko Win, Maartje Nielsen, Wolff Schmiegel, Guy Rosner, Karl Heinimann, Fiona Lalloo, Carlos A. Vaccaro, Elke Holinski-Feder, Leticia Moreira
Publikováno v:
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M & Okkels, H 2020, ' Correction : Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 9 . https://doi.org/10.1038/s41436-020-0892-4
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J-P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Dipòsit Digital de la UB
Universidad de Barcelona
Evans, D G, Crosbie, E, Hill, J & et al. 2019, ' Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. NATURE PUBLISHING GROUP
Genetics in Medicine
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, ten Broeke, S W, Plazzer, J P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. Nature Publishing Group
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J-P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Dipòsit Digital de la UB
Universidad de Barcelona
Evans, D G, Crosbie, E, Hill, J & et al. 2019, ' Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. NATURE PUBLISHING GROUP
Genetics in Medicine
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, ten Broeke, S W, Plazzer, J P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. Nature Publishing Group
Lynch syndrome (LS) results from pathogenic variants in the mismatch repair (MMR) genes and is the most common hereditary cancer syndrome, affecting an estimated 1 in 300 individuals. Pathogenic variants in each of the MMR genes path_MLH1, path_MSH2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::347fa11199294fa0eb757b6ff6ba0788
https://vbn.aau.dk/ws/files/394936730/Correction_Dominguez_Valentin_et_al._2020_.pdf
https://vbn.aau.dk/ws/files/394936730/Correction_Dominguez_Valentin_et_al._2020_.pdf
Autor:
Nerea, Matamala, Gema, Gomez-Mariano, Jose Antonio, Perez, Beatriz, Baladrón, María, Torres-Durán, Francisco Javier, Michel, Raquel, Saez, Jose María, Hernández-Pérez, Irene, Belmonte, Francisco, Rodriguez-Frias, Ignacio, Blanco, Pavel, Strnad, Sabina, Janciauskiene, Beatriz, Martinez-Delgado
Publikováno v:
American journal of respiratory cell and molecular biology. 63(4)
Alpha-1 antitrypsin deficiency (AATD) is an inherited condition characterized by reduced levels of serum AAT due to mutations in the
Autor:
Bibiana Quirant-Sánchez, Ignacio Blanco, Joan Matllo, Monica Piña, Oriol Estrada, Maria Dolade, Eva Martínez-Cáceres, Jaume Barallat, Gema Fernández-Rivas, Victoria González
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
PLoS ONE, Vol 15, Iss 12, p e0244348 (2020)
PLoS ONE
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Universitat Autònoma de Barcelona
PLoS ONE, Vol 15, Iss 12, p e0244348 (2020)
PLoS ONE
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Background The rapid spread of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) around the world has caused a global pandemic, infecting millions of individuals, with an unprecedented impact in health care systems worldwide. Healthcare wo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d015b539da7785bb23b1bd4d5dd1c1a
https://ddd.uab.cat/record/253220
https://ddd.uab.cat/record/253220
Autor:
Eric Legius, Neus Baena, Conxi Lázaro, Eduard Serra, Ignacio Blanco, Bernat Gel, Graciela Pi, Lluïsa Vilageliu, Mercè Pineda, Alex Negro, Daniel Grinberg, Hector Salvador, Elisabeth Castellanos, Inma Rosas, Hilde Brems, Guillem Pintos, Andreu Alibés
Publikováno v:
CLINICAL GENETICS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Dipòsit Digital de la UB
Universidad de Barcelona
Clinical Genetics
r-IGTP: Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Dipòsit Digital de la UB
Universidad de Barcelona
Clinical Genetics
r-IGTP: Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Children with neurofibromatosis type 1 (NF1) may exhibit an incomplete clinical presentation, making difficult to reach a clinical diagnosis. A phenotypic overlap may exist in children with other RASopathies or with other genetic conditions if only m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0919872b015311500d26be16d974edd
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=16693
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=16693
Autor:
Ignacio Blanco, Sergio Curi, Francisco Rodriguez-Frias, Cristina Esquinas, Sergio Cadenas, Ines Herrero, José Alberto Muños Hernández, M. I. Martínez, Francisco Javier Michel, Marc Miravitlles, Francisco Casas, Beatriz Lara, Beatriz Martinez-Delgado, Amparo Escribano, Francisco Dasí, Esther Rodríguez, Ana Bustamante, María E. Torres, Lourdes Lázaro
Publikováno v:
Archivos de Bronconeumología (English Edition). 53:13-18
Introduction and Objective REDAAT, the Spanish Registry of Patients with Alpha-1 Antitrypsin Deficiency, was set up in order to improve knowledge of this disease. This study is an evaluation of the registry and an analysis of its patient population.
Autor:
Helena Mazuelas, Imma Rosas, Meritxell Carrió, Ernest Terribas, Angel Raya, Eduard Serra, Josep Biayna, Ignacio Blanco, Yvonne Richaud-Patin, Senda Jiménez-Delgado, Bernat Gel, Conxi Lázaro, Leen Vendredy, Elisabeth Castellanos
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Stem Cell Reports
Stem Cell Reports, Vol 12, Iss 2, Pp 411-426 (2019)
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Universidad de Barcelona
Stem Cell Reports
Stem Cell Reports, Vol 12, Iss 2, Pp 411-426 (2019)
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Summary Neurofibromatosis type 1 (NF1) is a tumor predisposition genetic disease caused by mutations in the NF1 tumor suppressor gene. Plexiform neurofibromas (PNFs) are benign Schwann cell (SC) tumors of the peripheral nerve sheath that develop thro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8acd1bc377c36981a7b04aa2bebe7987
http://hdl.handle.net/2445/171527
http://hdl.handle.net/2445/171527
Autor:
Finlay A. Macrae, Gabriela Möslein, Jukka-Pekka Mecklin, D. Gareth Evans, Annika Lindblom, John Burn, Matilde Navarro, Fiona Lalloo, Lone Sunde, Paola Sala, Eivind Hovig, Gabriel Capellá, Einar Andreas Rødland, Julian R. Sampson, Lucio Bertario, Ian M. Frayling, Pål Møller, Laura Renkonen-Sinisalo, Kate Green, John-Paul Plazzer, Miriam Mints, Kukatharmini Tharmaratnam, James Hill, Ignacio Blanco, Sigve Nakken, Marta Pineda, Rolf H. Sijmons, Mark A. Jenkins, Maurizio Genuardi, Inge Bernstein, Toni T. Seppälä, Elke Holinski-Feder, Hans F. A. Vasen, Wouter H. de Vos tot Nederveen Cappel, Kirsi Pylvänäinen, Monika Morak, Juul T. Wijnen, Jacqueline Jeffries
Publikováno v:
Gut
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J R, Capella, G & Mallorca Group (http://mallorca-group.org) 2017, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer : a report from the prospective Lynch syndrome database ', Gut, vol. 66, no. 9, pp. 1657-1664 . https://doi.org/10.1136/gutjnl-2016-311403
Gut, 66(9), 1657-1664. BMJ PUBLISHING GROUP
Gut, 66(9), 1657-1664
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J R, Capella, G & Mallorca Group (http://mallorca-group.org) 2016, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database. ', Gut . https://doi.org/10.1136/gutjnl-2016-311403
Dipòsit Digital de la UB
Universidad de Barcelona
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J P, Pylvanainen, K, Genuardi, M, Mecklin, J P, Möslein, G, Sampson, J R & Capella, G 2016, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer : a report from the prospective Lynch syndrome database ', Gut . https://doi.org/10.1136/gutjnl-2016-311403
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J R, Capella, G & Mallorca Group (http://mallorca-group.org) 2017, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer : a report from the prospective Lynch syndrome database ', Gut, vol. 66, no. 9, pp. 1657-1664 . https://doi.org/10.1136/gutjnl-2016-311403
Gut, 66(9), 1657-1664. BMJ PUBLISHING GROUP
Gut, 66(9), 1657-1664
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, D G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos Tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J-P, Pylvanainen, K, Genuardi, M, Mecklin, J-P, Möslein, G, Sampson, J R, Capella, G & Mallorca Group (http://mallorca-group.org) 2016, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database. ', Gut . https://doi.org/10.1136/gutjnl-2016-311403
Dipòsit Digital de la UB
Universidad de Barcelona
Møller, P, Seppälä, T, Bernstein, I, Holinski-Feder, E, Sala, P, Evans, G, Lindblom, A, Macrae, F, Blanco, I, Sijmons, R, Jeffries, J, Vasen, H, Burn, J, Nakken, S, Hovig, E, Rødland, E A, Tharmaratnam, K, de Vos tot Nederveen Cappel, W H, Hill, J, Wijnen, J, Jenkins, M, Green, K, Lalloo, F, Sunde, L, Mints, M, Bertario, L, Pineda, M, Navarro, M, Morak, M, Renkonen-Sinisalo, L, Frayling, I M, Plazzer, J P, Pylvanainen, K, Genuardi, M, Mecklin, J P, Möslein, G, Sampson, J R & Capella, G 2016, ' Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer : a report from the prospective Lynch syndrome database ', Gut . https://doi.org/10.1136/gutjnl-2016-311403
OBJECTIVE: Today most patients with Lynch syndrome (LS) survive their first cancer. There is limited information on the incidences and outcome of subsequent cancers. The present study addresses three questions: (i) what is the cumulative incidence of