Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ignacio Blanco"'
Autor:
Concepción Violán, Pere Torán-Monserrat, Bibiana Quirant, Noemi Lamonja-Vicente, Lucía A. Carrasco-Ribelles, Carla Chacón, Josep Maria Manresa-Dominguez, Francesc Ramos-Roure, Rosalia Dacosta-Aguayo, Cristina Palacios-Fernández, Albert Roso-Llorach, Aleix Pujol, Dan Ouchi, Mónica Monteagudo, Pilar Montero-Alia, Rosa Garcia-Sierra, Fernando Arméstar, Maria Doladé, Nuria Prat, Josep Maria Bonet, Bonaventura Clotet, Ignacio Blanco, Marc Boigues-Pons, Nemesio Moreno-Millán, Julia G. Prado, Eva María Martínez Cáceres, for the ProHEpiC-19 study
Publikováno v:
BMC Infectious Diseases, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Background Understanding the immune response to the SARS-CoV-2 virus is critical for efficient monitoring and control strategies. The ProHEpic-19 cohort provides a fine-grained description of the kinetics of antibodies after SARS-CoV-2 infec
Externí odkaz:
https://doaj.org/article/b74f614863c3434bbbf833c28b70881f
Autor:
Marlene Guiraud, Athmane Bouroubi, Roxane Beauchamp, Arnaud Bocquet, Jean-Marc Grégoire, Isabelle Rauly-Lestienne, Ignacio Blanco, Pierre Wolkenstein, Anne-Marie Schmitt
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract 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 li
Externí odkaz:
https://doaj.org/article/d66d2cf1a4c74bed92a3ce2b1f743acb
Autor:
Toni T. Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, Finlay Macrae, D. Gareth Evans, Christina Therkildsen, Julian Sampson, Rodney Scott, John Burn, Gabriela Möslein, Inge Bernstein, Elke Holinski-Feder, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepistö, Charlotte Kvist Lautrup, Annika Lindblom, John-Paul Plazzer, Ingrid Winship, Douglas Tjandra, Lior H. Katz, Stefan Aretz, Robert Hüneburg, Stefanie Holzapfel, Karl Heinimann, Adriana Della Valle, Florencia Neffa, Nathan Gluck, Wouter H. de Vos tot Nederveen Cappel, Hans Vasen, Monika Morak, Verena Steinke-Lange, Christoph Engel, Nils Rahner, Wolff Schmiegel, Deepak Vangala, Huw Thomas, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Gabriel Capella, Marta Pineda, Matilde Navarro, Ignacio Blanco, Sanne ten Broeke, Maartje Nielsen, Ken Ljungmann, Sigve Nakken, Noralane Lindor, Ian Frayling, Eivind Hovig, Lone Sunde, Matthias Kloor, Jukka-Pekka Mecklin, Mette Kalager, Pål Møller
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-8 (2019)
Abstract Background Recent epidemiological evidence shows that colorectal cancer (CRC) continues to occur in carriers of pathogenic mismatch repair (path_MMR) variants despite frequent colonoscopy surveillance in expert centres. This observation conf
Externí odkaz:
https://doaj.org/article/5e7cff12646841c9a57d26447ff46ded
Autor:
Toni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, Heikki Järvinen, Laura Renkonen-Sinisalo, Inge Bernstein, Elke Holinski-Feder, Paola Sala, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons, Jacqueline Jeffries, Hans Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark Jenkins, Maurizio Genuardi, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Ian M. Frayling, John-Paul Plazzer, Julian R. Sampson, Gabriel Capella, Gabriela Möslein, Jukka-Pekka Mecklin, Pål Møller, in collaboration with The Mallorca Group
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss 1, Pp 1-10 (2017)
Abstract Background We have previously reported a high incidence of colorectal cancer (CRC) in carriers of pathogenic MLH1 variants (path_MLH1) despite follow-up with colonoscopy including polypectomy. Methods The cohort included Finnish carriers enr
Externí odkaz:
https://doaj.org/article/fa96c2aaea2f442f83f380ff0ada1046
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:
Conxi Lázaro, Angel Izquierdo, Gabriel Capellá, Alex Teulé, Joan Brunet, Francisco Quiles, Jesús del Valle, Esther Darder, Juana Fernández-Rodríguez, Miguel Angel Pujana, Detlev Schindler, Lídia Feliubadaló, Mónica Salinas, Ignacio Blanco
Publikováno v:
BMC Cancer, Vol 12, Iss 1, p 84 (2012)
BMC Cancer
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
BMC Cancer
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Background Genes that, when mutated, cause Fanconi anemia or greatly increase breast cancer risk encode for proteins that converge on a homology-directed DNA damage repair process. Mutations in the SLX4 gene, which encodes for a scaffold protein invo