Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lluís Forga"'
Autor:
Isabel Tena, María-Dolores Chiara, Josep Oriola, Elena Beristein, Cristóbal Bernardo-Castiñeira, María-José Molina-Garrido, María‐Agustina Sevilla, Carles Villabona, Ana S. Pitiot, Nuria Valdés, Inés Sáenz-de-Santa-María, Lluís Forga, Milagros Balbín, Bartolomé Scola, Aurora Astudillo, Irene Halperin, Paula Jiménez‐Fonseca, Carlos Suárez
Publikováno v:
Head & Neck.
BACKGROUND Succinate dehydrogenase subunit B (SDHB) immunohistochemistry was considered a valuable tool to identify patients with inherited paraganglioma/pheochromocytoma (PGL/PCC). However, previous studies jointly analyzed 2 related but clinically
Autor:
Emilio Ros, Marta Guasch-Ferré, Miguel Ruiz-Canela, Dolores Corella, Frank B. Hu, Miquel Fiol, Lluís Forga, Josep Basora, Ramon Estruch, Nerea Becerra-Tomás, José Lapetra, Nerea Martín-Calvo, Helmut Schröder, Montserrat Fitó, Jordi Salas-Salvadó, Olga Portolés, Enrique Gómez-Gracia, F. Aros, Lluis Serra-Majem
Background: The associations between dietary fat and cardiovascular disease have been evaluated in several studies, but less is known about their influence on the risk of diabetes.Objective: We examined the associations between total fat, subtypes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de5ad08a97e30e786f1d61ff31cddeee
https://hdl.handle.net/10668/10866
https://hdl.handle.net/10668/10866
Autor:
Erkuden Aranburu Urtasun, Carlos Prieto Martínez, María Mercado Gutiérrez, Mercedes Palacios Sarrasqueta, Ramón Angós Musgo, Miren Vicuña Arregui, Lluís Forga Llenas, Juan Pablo Martínez de Esteban, Francisco Sala Pericas, José Manuel Zozaya Urmeneta, Helena León Brito
Publikováno v:
Annals of Gastroenterology : Quarterly Publication of the Hellenic Society of Gastroenterology
Background Patients with type 1 diabetes mellitus (DM1) have an increased risk of celiac disease (CD). Since CD can be seronegative, more sensible tests for detection are needed. In seronegative patients, CD diagnosis may be difficult because of a la
Autor:
María Pilar Salvador Egea, Ana Puras Gil, Eduardo Layana Echezuri, Emma Anda Apiñariz, Lluís Forga Llenas, Edelmiro Menéndez Torre, Amaya Sainz de los Terreros, Ana Echegoyen Silanes
Publikováno v:
ISRN Oncology
Introduction. Navarra has the highest incidence of differentiated thyroid cancer in Spain. The aim of this study was to review its management carried out by the Navarra's multidisciplinary Thyroid Disease Unit, from 1987 to 2003. Material and Methods
Autor:
Eduardo Layana Echezuri, Edelmiro Menéndez Torre, Lluís Forga Llenas, Cristina Rodríguez Gutiérrez, José Manuel Zozaya Urmeneta, José María Martínez-Peñuela Virseda, Francisco Javier Jiménez Pérez, José Javier Pineda Arribas, Juan Pablo Martínez de Esteban, Miren Vicuña Arregui, David Carral Martínez
Publikováno v:
Gastroenterología y Hepatología. 33:6-11
Celiac disease (CD) presents a wide clinical spectrum. There are asymptomatic or oligosymptomatic forms, which are difficult to diagnose. Since patients with untreated CD can develop severe complications, early diagnosis of these forms is important.
Autor:
José Manuel Zozaya Urmeneta, Miren Vicuña Arregui, Lluís Forga Llenas, Juan Pablo Martínez de Esteban
Publikováno v:
Endocrinología y Nutrición. 56:437-440
Autor:
Juan Pablo, Martínez de Esteban, Marta Toni García, Lluís Forga Llenas, Patricia Munárriz Alcuaz, Emma Anda Apiñániz, María José Goñi Iriarte
Publikováno v:
Endocrinología y Nutrición. 55:510-513
Autoimmune polyendocrine syndrome type II (APS-II) is the most common immunoendocrinopathy syndrome. APS-II is defined by the development of two or more of the following entities: primary adrenal insufficiency (Addison's disease), Graves' disease, ty
Autor:
Rosa María Rodríguez Erdozain, Marta García Mouriz, Claudia Causso, Emma Anda Apiñániz, Lluís Forga Llenas
Publikováno v:
Revista Internacional de Andrología. 5:155-160
Resumen Introduccion La distrofia miotonica (DM1) es la forma heredada mas comun de distrofia muscular entre adultos. El defecto genetico causal consiste en la repeticion de un triplete CTG, en el cromosoma 19, que codifica una proteincinasa llamada
Autor:
Miren Vicuña, Arregui, Juan Pablo Martínez, de Esteban, Lluís Forga, Llenas, José Manuel Zozaya, Urmeneta
Publikováno v:
Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion. 56(10)
Autor:
Marta, Toni García, Emma, Anda Apiñániz, Juan, Pablo, Martínez, de Esteban, Patricia, Munárriz Alcuaz, María José, Goñi Iriarte, Lluís, Forga Llenas
Publikováno v:
Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion. 55(10)
Autoimmune polyendocrine syndrome type II (APS-II) is the most common immunoendocrinopathy syndrome. APS-II is defined by the development of two or more of the following entities: primary adrenal insufficiency (Addison's disease), Graves' disease, ty