Zobrazeno 1 - 10
of 16
pro vyhledávání: '"María Magallón"'
Autor:
María Magallón, Silvia Castillo-Corullón, Lucía Bañuls, Teresa Romero, Daniel Pellicer, Alberto Herrejón, María Mercedes Navarro-García, Cruz González, Francisco Dasí
Publikováno v:
Antioxidants, Vol 13, Iss 9, p 1071 (2024)
Background: Alpha-1 antitrypsin deficiency (AATD) is an inflammatory disorder where neutrophils play a key role. Excessive neutrophil activation leads to local hypoxia and tissue damage. Most research on neutrophil function has been conducted under a
Externí odkaz:
https://doaj.org/article/697449796d6a4ee189a8d0b91bafd4cb
Autor:
María Magallón, Silvia Castillo-Corullón, Lucía Bañuls, Daniel Pellicer, Teresa Romero, Carlos Martínez-Ferraro, María Mercedes Navarro-García, Alberto Herrejón, Cruz González, Francisco Dasí
Publikováno v:
Antioxidants, Vol 12, Iss 4, p 872 (2023)
Alpha-1 antitrypsin deficiency (AATD) is a neutrophilic inflammatory disorder that may result in local hypoxia, reactive oxygen and nitrogen species (ROS/RNS) production, and increased damage in adjacent tissues. This study aims to determine the impa
Externí odkaz:
https://doaj.org/article/10e0cf55726e4adfbb5dc60829a3fc92
Autor:
María Torres-Durán, José Luis Lopez-Campos, Miriam Barrecheguren, Marc Miravitlles, Beatriz Martinez-Delgado, Silvia Castillo, Amparo Escribano, Adolfo Baloira, María Mercedes Navarro-Garcia, Daniel Pellicer, Lucía Bañuls, María Magallón, Francisco Casas, Francisco Dasí
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-15 (2018)
Abstract Background Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circulating alpha-1 antitrypsin (AAT) levels, significantly increasing the risk of serious lung and/or liver disease in children and adul
Externí odkaz:
https://doaj.org/article/43b4f3b8d6ba46e19b5e09e38da390f5
Autor:
María Magallón, Sara Pastor, Ana Esther Carrión, Lucía Bañuls, Daniel Pellicer, Silvia Castillo, Sergio Bondía, María Mercedes Navarro-García, Cruz González, Francisco Dasí
Publikováno v:
Journal of Clinical Medicine. 11:7322
Sara Pastor was not included as an author in the original publication [...]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::673bab64f690907e5a502f54ebcfb98e
https://doi.org/10.3390/jcm11247322
https://doi.org/10.3390/jcm11247322
Autor:
Cruz González, Sergio Bondia, María Mercedes Navarro-García, Lucía Bañuls, Daniel Pellicer, Silvia Castillo, Francisco Dasí, María Magallón Serrano
Publikováno v:
Molecular pathology and functional genomics.
Introduction: Alpha-1 antitrypsin deficiency (AATD) is a rare respiratory condition characterized by abnormal inflammation, where neutrophils play a key role. Excessive neutrophil activation leads to an increase in the oxygen (O2) intake, causing loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433ecf5bc3e2f15e72a2c6faa9f9e4eb
https://doi.org/10.1183/13993003.congress-2021.pa2396
https://doi.org/10.1183/13993003.congress-2021.pa2396
Autor:
Cruz González, Francisco Dasí, María Mercedes Navarro-García, Lucía Bañuls, Sergi Bondia, Silvia Castillo, María Magallón, Daniel Pellicer
Publikováno v:
Molecular pathology and functional genomics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dc566bb0b45453d4d6343a8f21e5e7f
https://doi.org/10.1183/13993003.congress-2021.pa668
https://doi.org/10.1183/13993003.congress-2021.pa668
Autor:
Cruz González, María Mercedes Navarro-García, Lucía Bañuls, Francisco Dasí, Daniel Pellicer, Silvia Castillo, María Magallón
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 2577, p 2577 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine
Gene therapy is an alternative therapy in many respiratory diseases with genetic origin and currently without curative treatment. After five decades of progress, many different vectors and gene editing tools for genetic engineering are now available.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f714e590e5541e3359587977f66fe8
https://www.mdpi.com/2077-0383/9/8/2577
https://www.mdpi.com/2077-0383/9/8/2577
Autor:
María Magallón, Lucía Bañuls, Silvia Castillo, María Mercedes Navarro-García, Cruz González, Francisco Dasí
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 5906, p 5906 (2021)
Journal of Clinical Medicine
Journal of Clinical Medicine
In the 1970s, the term “rare disease” was coined to describe a category of inherited metabolic diseases with low prevalence and a wide range of symptoms [...]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e165ba0e28a17344330db144a4ed10
https://doi.org/10.3390/jcm10245906
https://doi.org/10.3390/jcm10245906
Publikováno v:
Journal of Clinical Medicine
Numerous studies over the years have shown that oxidative stress plays a major role in the development of the disease. Oxidative stress involvement in COPD opens up the possibility of using antioxidant therapies in the treatment of the disease. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c7479cb849b0ea13686beca83d9364
https://pubmed.ncbi.nlm.nih.gov/31766150
https://pubmed.ncbi.nlm.nih.gov/31766150
Autor:
María Magallón, Silvia Castillo, Sara Pastor, Daniel Pellicer, María Mercedes Navarro-García, Lucía Bañuls, Francisco Jose Dasi Fernandez, Amparo Escribano
Publikováno v:
Molecular pathology and funct. genomics.
Introduction: Alpha-1 antitrypsin (AATD) deficiency is an inherited condition that leads to decreased circulating AAT levels, significantly increasing the risk of lung and liver disease. AATD is underdiagnosed. Severity of symptoms in AATD patients a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f50bc3104ff455f10a8bea9a678c64a
https://doi.org/10.1183/13993003.congress-2019.pa5415
https://doi.org/10.1183/13993003.congress-2019.pa5415