Zobrazeno 1 - 10
of 407
pro vyhledávání: '"A, Hermida Ameijeiras"'
Autor:
Nestor Vazquez-Agra, Anton Cruces-Sande, Sofia Barbosa-Gouveia, Jose-Enrique Lopez-Paz, Miguel Camafort, Emilio Casariego-Vales, Antonio Pose-Reino, Alvaro Hermida-Ameijeiras
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract High lipoprotein(a) (Lp(a)) levels are associated with an increased risk of arterial hypertension (AHT) and atherosclerotic cardiovascular disease. However, little is known about the detailed profile of AHT based on Lp(a) levels. This observ
Externí odkaz:
https://doaj.org/article/108fd1f279154d4da9b1c7e7d505cf76
Autor:
Carlos Rábade-Castedo, Carlos Zamarrón-Sanz, Álvaro Hermida-Ameijeiras, Romina Abelleira-Paris, Ana Casal-Mouriño, Lucia Ferreiro-Fernández, Nuria Rodríguez-Núñez, Jorge Ricoy-Gabaldón, María Elena Toubes-Navarro, José Manuel Álvarez-Dobaño, Luis Valdés-Cuadrado
Publikováno v:
Tobacco Induced Diseases, Vol 22, Iss February, Pp 1-11 (2024)
Introduction The smoker's narrative during smoking quitting provides insight into aspects not fully explored in daily clinical practice. The aim of the study was to analyze the smoker narrative using two types of methodologies: content analysis and g
Externí odkaz:
https://doaj.org/article/5a24fe575b514de09e73bc3381ce8388
Autor:
López-Valverde, Laura, Vázquez-Mosquera, María E., Colón-Mejeras, Cristóbal, Bravo, Susana B., Barbosa-Gouveia, Sofía, Álvarez, J. Víctor, Sánchez-Martínez, Rosario, López-Mendoza, Manuel, López-Rodríguez, Mónica, Villacorta-Argüelles, Eduardo, Goicoechea-Diezhandino, María A., Guerrero-Márquez, Francisco J., Ortolano, Saida, Leao-Teles, Elisa, Hermida-Ameijeiras, Álvaro, Couce, María L.
Publikováno v:
In Translational Research July 2024 269:47-63
Autor:
Stephanie Maissen-Abgottspon, Raphaela Muri, Michel Hochuli, Péter Reismann, András Gellért Barta, Ismail Mucahit Alptekin, Álvaro Hermida-Ameijeiras, Alessandro P. Burlina, Alberto B. Burlina, Chiara Cazzorla, Jessica Carretta, Roman Trepp, Regula Everts
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-12 (2023)
Abstract Background Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabolism of phenylalanine (Phe). To date, findings regarding health-related quality of life (HRQoL) in adults with early-treated classical PKU are discrepa
Externí odkaz:
https://doaj.org/article/9de6a35a1c3e47259c17ab8c1cb6dde5
Autor:
Antón Cruces-Sande, Pablo Garrido-Gil, Germán Sierra-Paredes, Néstor Vázquez-Agra, Álvaro Hermida-Ameijeiras, Antonio Pose-Reino, Estefanía Méndez-Álvarez, Ramón Soto-Otero
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8309 (2024)
Copper is a trace element whose electronic configuration provides it with essential structural and catalytic functions. However, in excess, both its high protein affinity and redox-catalyzing properties can lead to hazardous consequences. In addition
Externí odkaz:
https://doaj.org/article/4fb8000d98bc4f83a183cb8a61b1fdd2
Autor:
Fernandez-Crespo, Silvia, Vazquez-Agra, Nestor, Marques-Afonso, Ana-Teresa, Cruces-Sande, Anton, Martinez-Olmos, Miguel-Angel, Araujo-Vilar, David, Hermida-Ameijeiras, Alvaro
Publikováno v:
In Medicina Clinica 7 December 2023 161(11):470-475
Autor:
Rocío Blanco, Yolanda Rico-Ramírez, Álvaro Hermida-Ameijeiras, Israa Mahmoud Sanad Abdullah, Kolja Lau, Jorge Alvarez-Rubio, Elena Fortuny, Amparo Martínez-Monzonís, Albina Nowak, Peter Nordbeck, Carlos Veras-Burgos, Jaume Pons-Llinares, Emiliano Rossi, Fiama Caimi-Martínez, Teresa Bosch-Rovira, Marta Alamar-Cervera, Virginia Ruiz-Pizarro, Laura Torres-Juan, Damian Heine-Suñer, Tomás Ripoll-Vera
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4299 (2024)
The p.Arg301Gln variant in the α -galactosidase A gene (GLA) has been poorly described in the literature. The few reports show controversial information, with both classical and nonclassical Anderson–Fabry Disease (AFD) presentation patterns. The
Externí odkaz:
https://doaj.org/article/2f0e8a45e1a5487b9b0ecaab22b81f0c
Autor:
Everardo Josué Díaz-López, Rocio Villar-Taibo, Gemma Rodriguez-Carnero, Antia Fernandez-Pombo, Roberto Garcia-Peino, Manuel Narciso Blanco-Freire, Alberto Pena-Dubra, Teresa Prado-Moraña, Irea- Fernández-Xove, Edurne Pérez-Béliz, Jose Manuel Cameselle-Teijeiro, Alvaro Hermida-Ameijeiras, Miguel Angel Martinez-Olmos
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Severe hypokalaemia causing rhabdomyolysis (RML) in primary aldosteronism (PA) is a rare entity, and only a few cases have been reported over the last four decades. This systematic review and case report aims to gather all published data regarding a
Externí odkaz:
https://doaj.org/article/e85169f7c3564f719ec1345160fc1e69
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