Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Eva Tosco-Herrera"'
Autor:
Eva Suarez-Pajes, Itahisa Marcelino-Rodriguez, Elisa Hernández Brito, Silvia Gonzalez-Barbuzano, Melody Ramirez-Falcon, Eva Tosco-Herrera, Luis A. Rubio-Rodríguez, María Luisa Briones, Olga Rajas, Luis Borderías, Jose Ferreres, Antoni Payeras, Leonardo Lorente, Javier Aspa, Jose M. Lorenzo Salazar, José Manuel Valencia-Gallardo, Nieves Carbonell, Jorge L. Freixinet, Felipe Rodríguez de Castro, Jordi Solé Violán, Carlos Flores, Carlos Rodríguez-Gallego
Publikováno v:
Respiratory Research, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Community-acquired pneumonia (CAP) is associated with high morbidity and hospitalization rate. In infectious diseases, host genetics plays a critical role in susceptibility and immune response, and the immune pathways involved are
Externí odkaz:
https://doaj.org/article/92f8bc406f5d40ba8d66573f3495e477
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Idiopathic pulmonary fibrosis (IPF) is a chronic, rare progressive lung disease, characterized by lung scarring and the irreversible loss of lung function. Two anti-fibrotic drugs, nintedanib and pirfenidone, have been demonstrated to slow down disea
Externí odkaz:
https://doaj.org/article/f602b37548cb4413b6512dd7fdc51724
Autor:
Alejandro Mendoza-Alvarez, Eva Tosco-Herrera, Adrian Muñoz-Barrera, Luis A. Rubio-Rodríguez, Aitana Alonso-Gonzalez, Almudena Corrales, Antonio Iñigo-Campos, Lourdes Almeida-Quintana, Elena Martin-Fernandez, Dara Martinez-Beltran, Eva Perez-Rodriguez, Ariel Callero, Jose C. Garcia-Robaina, Rafaela González-Montelongo, Itahisa Marcelino-Rodriguez, Jose M. Lorenzo-Salazar, Carlos Flores
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Hereditary angioedema (HAE) is a rare disease where known causes involve C1 inhibitor dysfunction or dysregulation of the kinin cascade. The updated HAE management guidelines recommend performing genetic tests to reach a precise diagnosis. Unfortunat
Externí odkaz:
https://doaj.org/article/a93421c7594a4745b4d04a76cb37acd5
Autor:
Eva Tosco‐Herrera, Adrián Muñoz‐Barrera, David Jáspez, Luis A. Rubio‐Rodríguez, Alejandro Mendoza‐Alvarez, Hector Rodriguez‐Perez, Jonathan Jou, Antonio Iñigo‐Campos, Almudena Corrales, Laura Ciuffreda, Francisco Martinez‐Bugallo, Carol Prieto‐Morin, Víctor García‐Olivares, Rafaela González‐Montelongo, Jose Miguel Lorenzo‐Salazar, Itahisa Marcelino‐Rodriguez, Carlos Flores
Publikováno v:
Human mutationREFERENCES. 43(12)
Most causal variants of Mendelian diseases are exonic. Whole-exome sequencing (WES) has become the diagnostic gold standard, but causative variant prioritization constitutes a bottleneck. Here we assessed an in-house sample-to-sequence pipeline and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7af15fb344c1dd5479b12abbf21e69
https://pubmed.ncbi.nlm.nih.gov/36054330
https://pubmed.ncbi.nlm.nih.gov/36054330
Autor:
Eva Suarez-Pajes, Eva Tosco-Herrera, Melody Ramirez-Falcon, Silvia Gonzalez-Barbuzano, Tamara Hernandez-Beeftink, Beatriz Guillen-Guio, Jesús Villar, Carlos Flores
Publikováno v:
Journal of Clinical Medicine. 12:3713
Acute respiratory distress syndrome (ARDS) is a life-threatening lung condition that arises from multiple causes, including sepsis, pneumonia, trauma, and severe coronavirus disease 2019 (COVID-19). Given the heterogeneity of causes and the lack of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f12d88d53e3e40f79b8453e84060a14
https://doi.org/10.3390/jcm12113713
https://doi.org/10.3390/jcm12113713