Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sara Chocrón"'
Autor:
Vega García López, Dunia Jové Gómez, Belén Marin Martinez, Sara Chocrón Miño, Andrea Castillo Sabogal, Angela Ibarra García
Publikováno v:
Archivos de Prevención de Riesgos Laborales, Vol 27, Iss 2 (2024)
Introducción: La enfermedad pulmonar intersticial difusa (EPID) describe un amplio grupo de trastornos con inflamación y fibrosis pulmonar. La asbestosis y la silicosis son las principales causas por exposición laboral. El objetivo de este trabajo
Externí odkaz:
https://doaj.org/article/bab0175b25ea487695cfced35b1d4049
Autor:
Enrique Casado, Carlos Gómez-Alonso, Guillem Pintos-Morell, Rosa Bou-Torrent, Ana Coral Barreda-Bonis, José Vicente Torregrosa, José Jesús Broseta-Monzó, Pedro Arango-Sancho, Sara Chocrón-de-Benzaquen, Yoko Olmedilla-Ishishi, Begoña Soler-López
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-15 (2023)
Abstract Background There are currently no models for the transition of patients with metabolic bone diseases (MBDs) from paediatric to adult care. The aim of this project was to analyse information on the experience of physicians in the transition o
Externí odkaz:
https://doaj.org/article/25428c7cb49d4af693e09da1738c21c1
Autor:
Alejandro García Castaño, Gustavo Pérez de Nanclares, Leire Madariaga, Mireia Aguirre, Álvaro Madrid, Sara Chocrón, Inmaculada Nadal, Mercedes Navarro, Elena Lucas, Julia Fijo, Mar Espino, Zilac Espitaletta, Víctor García Nieto, David Barajas de Frutos, Reyner Loza, Guillem Pintos, Luis Castaño, RenalTube Group, Gema Ariceta
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173581 (2017)
Type III Bartter syndrome (BS) is an autosomal recessive renal tubule disorder caused by loss-of-function mutations in the CLCNKB gene, which encodes the chloride channel protein ClC-Kb. In this study, we carried out a complete clinical and genetic c
Externí odkaz:
https://doaj.org/article/dc0787dd88464a0599e86f65e6e64df2
Autor:
Gómez, Dunia Jové1, Miño, Sara Chocrón1, Sabogal, Andrea Castillo1, García, Angela Ibarra2, López, Vega García1 vgarcial@navarra.es, Martinez, Belén Marin3
Publikováno v:
Archivos de Prevención de Riesgos Laborales. abr-jun2024, Vol. 27 Issue 2, p173-189. 17p. 5 Charts, 1 Graph.
Autor:
Juan, Gómez, Helena, Gil-Peña, Fernando, Santos, Eliecer, Coto, Ana, Arango, Olaya, Hernandez, Julián, Rodríguez, Inmaculada, Nadal, Virginia, Cantos, Sara, Chocrón, Inés, Vergara, Álvaro, Madrid, Carlos, Vazquez, Luz E, González
Publikováno v:
Pediatric research. 83(1-1)
This corrects the article DOI: 10.1038/pr.2015.243.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8050c23dc31d99d4c479b4fea39e6c02
https://pubmed.ncbi.nlm.nih.gov/26571219
https://pubmed.ncbi.nlm.nih.gov/26571219
Autor:
Enrique Rodríguez-Rubio, Helena Gil-Peña, Sara Chocron, Leire Madariaga, Francisco de la Cerda-Ojeda, Marta Fernández-Fernández, Carmen de Lucas-Collantes, Marta Gil, María Isabel Luis-Yanes, Inés Vergara, Juan David González-Rodríguez, Susana Ferrando, Montserrat Antón-Gamero, Marta Carrasco Hidalgo-Barquero, Angustias Fernández-Escribano, Mº Ángeles Fernández-Maseda, Laura Espinosa, Aniana Oliet, Antonio Vicente, Gema Ariceta, Fernando Santos, RenalTubeGroup
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Abstract Background X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in PHEX gene leading tohypophosphatemia and high renal loss of phosphate. Rickets and growth retardation are the major manifestation
Externí odkaz:
https://doaj.org/article/66beb24ba93343f7bb984a5886faa736
Autor:
Enrique Rodríguez-Rubio, Helena Gil-Peña, Sara Chocron, Leire Madariaga, Francisco de la Cerda-Ojeda, Marta Fernández-Fernández, Carmen de Lucas-Collantes, Marta Gil, María Isabel Luis-Yanes, Inés Vergara, Juan David González-Rodríguez, Susana Ferrando, Montserrat Antón-Gamero, Marta Carrasco Hidalgo-Barquero, Angustias Fernández-Escribano, Mº Ángeles Fernández-Maseda, Laura Espinosa, Aniana Oliet, Antonio Vicente, Gema Ariceta, Fernando Santos, RenalTubeGroup
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Externí odkaz:
https://doaj.org/article/eb5e00b90aaa4a16b2525a596189b7a3