Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Eva Perez-Rodriguez"'
Autor:
Eva Suarez-Pajes, Claudio Díaz-García, Héctor Rodríguez-Pérez, Jose M. Lorenzo-Salazar, Itahisa Marcelino-Rodríguez, Almudena Corrales, Xiuwen Zheng, Ariel Callero, Eva Perez-Rodriguez, Jose C. Garcia-Robaina, Rafaela González-Montelongo, Carlos Flores, Beatriz Guillen-Guio
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Despite asthma has a considerable genetic component, an important proportion of genetic risks remain unknown, especially for non-European populations. Canary Islanders have the largest African genetic ancestry observed among Southwestern Eur
Externí odkaz:
https://doaj.org/article/ed784de2a5304a789e3bd2fc583edee2
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:
Itahisa Marcelino-Rodriguez, Ariel Callero, Alejandro Mendoza-Alvarez, Eva Perez-Rodriguez, Javier Barrios-Recio, Jose C. Garcia-Robaina, Carlos Flores
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/becd8094a1654055b354007e61749b7b
Autor:
Itahisa Marcelino-Rodriguez, Ariel Callero, Alejandro Mendoza-Alvarez, Eva Perez-Rodriguez, Javier Barrios-Recio, Jose C. Garcia-Robaina, Carlos Flores
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Recurrent episodes of bradykinin-mediated angioedema (Bk-AE) can associate with acquired or hereditary conditions, the former most commonly developing secondarily to a pharmacological treatment. Despite successful genomic advances that have led to th
Externí odkaz:
https://doaj.org/article/798ad424c2624958add8f502c894673d
Autor:
Almudena Corrales, José M. Lorenzo-Salazar, José Carlos García-Robaina, Adrián Muñoz-Barrera, Alejandro Mendoza-Alvarez, Antonio Íñigo-Campos, Ariel Callero, Itahisa Marcelino-Rodríguez, Luis A. Rubio-Rodríguez, Eva Perez-Rodriguez, Carlos Flores, Rafaela González-Montelongo
Publikováno v:
Journal of Medical Internet Research, Vol 22, Iss 10, p e19040 (2020)
Journal of Medical Internet Research
Journal of Medical Internet Research
Background Hereditary angioedema is a rare genetic condition caused by C1 esterase inhibitor deficiency, dysfunction, or kinin cascade dysregulation, leading to an increased bradykinin plasma concentration. Hereditary angioedema is a poorly recognize
Autor:
Itahisa Marcelino-Rodriguez, Ariel Callero, Alejandro Mendoza-Alvarez, Eva Perez-Rodriguez, Javier Barrios-Recio, Jose C. Garcia-Robaina, Carlos Flores
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics, Vol 11 (2020)
Autor:
Alejandro Mendoza-Alvarez, Adrián Muñoz-Barrera, Luis Alberto Rubio-Rodríguez, Itahisa Marcelino-Rodriguez, Almudena Corrales, Antonio Iñigo-Campos, Ariel Callero, Eva Perez-Rodriguez, Jose Carlos Garcia-Robaina, Rafaela González-Montelongo, Jose Miguel Lorenzo-Salazar, Carlos Flores
BACKGROUND Hereditary angioedema is a rare genetic condition caused by C1 esterase inhibitor deficiency, dysfunction, or kinin cascade dysregulation, leading to an increased bradykinin plasma concentration. Hereditary angioedema is a poorly recognize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e15f05808b3180d44d1bfd0fb1a8639b
https://doi.org/10.2196/preprints.19040
https://doi.org/10.2196/preprints.19040
Autor:
Maria Pino-Yanes, Ariel Callero, Marta Espinilla-Peña, Eva Perez-Rodriguez, Rafaela González-Montelongo, Carlos Flores, Almudena Corrales, Héctor Rodríguez-Pérez, Jesús Villar, Tamara Hernández-Beeftink, José M. Lorenzo-Salazar, Beatriz Guillen-Guio, Itahisa Marcelino-Rodríguez
Publikováno v:
American journal of physiology. Lung cellular and molecular physiology. 318(5)
The prevalence of asthma symptoms in Canary Islanders, a southwestern European population from Spain, is almost three times higher than the country average. Because the genetic risks identified so far explain −4; odds ratio (OR) = 2.05; 95% confide
Autor:
Victoria Del Pozo, Maria Pino-Yanes, Javier Perez-Garcia, Javier Korta-Murua, Ruperto González-Pérez, Jesús Villar, José A Cañas, Fabián Lorenzo-Díaz, Antonio Espuela-Ortiz, Julia Alcoba-Florez, Hemily Izaguirre-Flores, Inmaculada Sánchez-Machín, Olaia Sardón, Lorenzo Pérez-Negrín, Mariano Hernandez-Ferrer, Javier Barrios-Recio, Paula Corcuera, Esther Herrera-Luis, Eva Perez-Rodriguez, Elena Martín-González, Elena Mederos-Luis, Lina Inmaculada Pérez Méndez, Paloma Poza-Guedes, Purificación Ramírez-Martín, Luis Manuel González García, José María Hernández-Pérez, José M Rodrigo Muñoz, Ariel Callero
Publikováno v:
Journal of Personalized Medicine
Volume 10
Issue 3
Journal of Personalized Medicine, Vol 10, Iss 123, p 123 (2020)
Volume 10
Issue 3
Journal of Personalized Medicine, Vol 10, Iss 123, p 123 (2020)
Asthma exacerbations are a major contributor to the global disease burden, but no significant predictive biomarkers are known. The Genomics and Metagenomics of Asthma Severity (GEMAS) study aims to assess the role of genomics and the microbiome in se
Autor:
Felipe Heras-Mendaza, Juan Antonio Martinez-Tadeo, José Carlos García-Robaina, Eva Perez-Rodriguez, Luis Conde-Salazar, Ariel Callero
Publikováno v:
Asia Pacific Allergy