Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Aitana Alonso-Gonzalez"'
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
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-12 (2019)
Abstract Background Attention-Deficit Hyperactivity Disorder (ADHD) is a complex neurodevelopmental disorder (NDD) which may significantly impact on the affected individual’s life. ADHD is acknowledged to have a high heritability component (70–80
Externí odkaz:
https://doaj.org/article/4cc8faac685f41588b4b3cb38743d476
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Background: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by its significant social impact and high heritability. The latest meta-analysis of ASD GWAS (genome-wide association studies) has revealed the association of s
Externí odkaz:
https://doaj.org/article/c663828b36f44436aa9c2cc7c44a4c82
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder (NDD) defined by impairments in social communication and social interactions, accompanied by repetitive behavior and restricted interests. ASD is characterized by its clinical and etiolo
Externí odkaz:
https://doaj.org/article/366e28c8d565474b98bc845990fda9f5
Autor:
Rocío Martínez-Regueiro, Jorge Amigo, Javier González-Peñas, Angel Carracedo, M. Parellada, Montse Fernández-Prieto, Aitana Alonso-Gonzalez, Celso Arango, Cristina Rodriguez-Fontenla, Manuel Calaza
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Scientific Reports
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)
Scientific Reports
De novo mutations (DNMs), including germinal and postzygotic mutations (PZMs), are a strong source of causality for Autism Spectrum Disorder (ASD). However, the biological processes involved behind them remain unexplored. Our aim was to detect DNMs (
Autor:
Montse Fernández Prieto, Ángel Carracedo Álvarez, Javier Gonzalez Penas, Mara Parellada, Cristina Rodriguez Fontenla, Manuel Calaza Cabanas, Rocio Martinez Regueiro, Aitana Alonso Gonzalez, Jorge Amigo
De novo mutations (DNMs), including germinal and postzygotic mutations (PZMs), are a strong source of causality for Autism Spectrum Disorder (ASD). However, the biological processes involved behind them remain unexplored. Our aim was to detect DNMs (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea69565e859b68f85426eb080ef08813
https://doi.org/10.1101/2020.05.21.107987
https://doi.org/10.1101/2020.05.21.107987
Autor:
Javier Costas, Montse Fernández-Prieto, Maria J Penzol, Aitana Alonso-Gonzalez, Angel Carracedo, Alicia García-Alcón, Celso Arango, Javier González-Peñas, Mara Parellada, Julio Rodríguez, Cristina Rodriguez-Fontenla
Publikováno v:
Translational Psychiatry
Translational Psychiatry, Vol 10, Iss 1, Pp 1-9 (2020)
Translational Psychiatry, Vol 10, Iss 1, Pp 1-9 (2020)
There is great phenotypic heterogeneity within autism spectrum disorders (ASD), which has led to question their classification into a single diagnostic category. The study of the common genetic variation in ASD has suggested a greater contribution of
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-12 (2019)
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-12 (2019)
Background Attention-Deficit Hyperactivity Disorder (ADHD) is a complex neurodevelopmental disorder (NDD) which may significantly impact on the affected individual’s life. ADHD is acknowledged to have a high heritability component (70–80%). Recen
Autor:
Mara Parellada, Javier González-Peñas, Jorge Amigo, Aitana Alonso-Gonzalez, Angel Carracedo, Cristina Rodriguez-Fontenla
Publikováno v:
European Neuropsychopharmacology. 29:S1119