Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maria Liz Leoz"'
Autor:
Enrique Quintero, Marta Carrillo, Maria-Liz Leoz, Joaquin Cubiella, Carla Gargallo, Angel Lanas, Luis Bujanda, Antonio Z Gimeno-García, Manuel Hernández-Guerra, David Nicolás-Pérez, Inmaculada Alonso-Abreu, Juan Diego Morillas, Francesc Balaguer, Alfonso Muriel, Oncology Group of the Asociación Española de Gastroenterología (AEG)
Publikováno v:
PLoS Medicine, Vol 13, Iss 5, p e1002008 (2016)
First-degree relatives (FDR) of patients with colorectal cancer have a higher risk of developing colorectal cancer than the general population. For this reason, screening guidelines recommend colonoscopy every 5 or 10 y, starting at the age of 40, de
Externí odkaz:
https://doaj.org/article/57db84c41e094a59a9a3b721748b299e
Autor:
Anna Serradesanferm, Antoni Castells, Xavier Bessa, Maria Liz Leoz, Maria Pellise, Sabela Carballal, Ariadna Sánchez, Francesc Balaguer, Josep M. Augé, Teresa Ocaña, Angels Pozo, Josep Llach, María López-Cerón, Jaume Grau, Liseth Rivero-Sánchez, Leticia Moreira, Miriam Cuatrecasas
Publikováno v:
Endoscopy. 49:44-53
Background and study aims Serrated polyposis syndrome (SPS) is a high risk condition for colorectal cancer (CRC). Surveillance strategies for patients with serrated lesions remain controversial. We aimed to evaluate a diagnostic strategy to detect SP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::493110f80e9e6b3608b5054ac9b69909
https://doi.org/10.1055/s-0042-115640
https://doi.org/10.1055/s-0042-115640
Autor:
Maria Liz Leoz, Francesc Balaguer, Leticia Moreira, Ariadna Sánchez, Maria Pellise, Sabela Carballal, Teresa Ocaña, Antoni Castells, Lucía Ruano
Publikováno v:
Gastroenterología y Hepatología. 39:481-493
The most common hereditary gastrointestinal cancers are colorectal, mainly hereditary nonpolyposis colorectal cancer (Lynch syndrome) and familial adenomatous polyposis. Other extracolonic neoplasms, including the gastric and pancreatic adenocarcinom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5b75b3a01925d76eb9afd315cc8323a
https://doi.org/10.1016/j.gastrohep.2015.11.009
https://doi.org/10.1016/j.gastrohep.2015.11.009
Autor:
Ariadna Sánchez, Leticia Moreira, Maria Pellise, Maria Liz Leoz, Antoni Castells, Francesc Balaguer, Sabela Carballal, Lucía Ruano, Teresa Ocaña
Publikováno v:
Gastroenterología y Hepatología (English Edition). 39:481-493
The most common hereditary gastrointestinal cancers are colorectal, mainly hereditary nonpolyposis colorectal cancer (Lynch syndrome) and familial adenomatous polyposis. Other extracolonic neoplasms, including the gastric and pancreatic adenocarcinom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa28c01180af4e3ec839059333106a4f
https://doi.org/10.1016/j.gastre.2016.06.010
https://doi.org/10.1016/j.gastre.2016.06.010
Autor:
Mariano González, Maria Liz Leoz, María López-Cerón, Eloisa Moya, Francesc Balaguer, Daniel Rodríguez-Alcalde, Inés Castro, Pilar Esteban, Liseth Rivero-Sánchez, Enrique Quintero, Luis Bujanda, Lucía Cid, Virginia Piñol, Victoria Gonzalo, Rodrigo Jover, Jorge López-Vicente, Joaquín Cubiella, Xavier Bessa, Maria Pellise, Antoni Castells, Lorena Rodríguez, Francisco Rodríguez-Moranta, Joan Clofent, Luis Hernández, Susana Oquiñena, Sabela Carballal, Leticia Moreira, Carmen Poves, Miriam Cuatrecasas, F. Fernandez
Publikováno v:
Gut. 65:1829-1837
Objective Serrated polyposis syndrome (SPS) is associated with an increased colorectal cancer (CRC) risk, although the magnitude of the risk remains uncertain. Whereas intensive endoscopic surveillance for CRC prevention is advised, predictors that i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5ee4487e339ec571feffff4d5155190
https://doi.org/10.1136/gutjnl-2015-309647
https://doi.org/10.1136/gutjnl-2015-309647
Publikováno v:
Colorectal Cancer. 3:57-76
SUMMARY Colorectal cancer (CRC) is one of the most common malignancies and the second-leading cause of cancer death in both sexes in developed countries. Over the last 25 years, highly penetrant monogenic germline mutations that predispose to CRC and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f38a643edbf7baefb54094203386ceb
https://doi.org/10.2217/crc.13.80
https://doi.org/10.2217/crc.13.80
Publikováno v:
Gastroenterología y Hepatología. 36:580-586
Desmoid tumors are currently the main cause of morbidity and mortality in patients with familial adenomatous polyposis. More than 10% of these patients will develop these tumors during their lifetime and more than a third will suffer their consequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8a683fa184958760caf658493aa7e61
https://doi.org/10.1016/j.gastrohep.2012.12.005
https://doi.org/10.1016/j.gastrohep.2012.12.005
Autor:
Rosa Miquel, Josep Llach, Maria Liz Leoz, Cristina Rodríguez de Miguel, Graciela Martínez-Pallí, Oriol Sendino, Josep M. Bordas, Andrés Cárdenas, Domingo Balderramo, Antoni Rimola, Miguel Navasa
Publikováno v:
Liver Transplantation. 19:199-206
In this descriptive study, we examined the role of single-operator cholangioscopy (SOC) in the evaluation of biliary complications after liver transplantation (LT). We prospectively included adult recipients of deceased donor LT who were referred for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3317e63df902c48b512518368672e2aa
https://doi.org/10.1002/lt.23585
https://doi.org/10.1002/lt.23585
Autor:
Maria Liz Leoz, Miriam Cuatrecasas, L Aguilera, Sabela Carballal, Isis K. Araujo, D Avila Carpio Ansel, Joan Llach, Maria Pellise, Elena Ricart, Liseth Rivero-Sánchez
Publikováno v:
Endoscopy. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5994515389c1468e921a33356217a9f
https://doi.org/10.1055/s-0035-1566060
https://doi.org/10.1055/s-0035-1566060
Publikováno v:
The Application of Clinical Genetics
Familial adenomatous polyposis (FAP) is an inherited disorder that represents the most common gastrointestinal polyposis syndrome. Germline mutations in the APC gene were initially identified as responsible for FAP, and later, several studies have al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e6ef90ac761a10ab53377889c5c748
https://pubmed.ncbi.nlm.nih.gov/25931827
https://pubmed.ncbi.nlm.nih.gov/25931827