Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel Alkassam"'
Autor:
Javier Garcia-Fernandez, Ruth Saez-Maleta, Ana Merino-Merino, Ricardo Salgado-Aranda, Jose-Angel Perez-Rivera, Daniel AlKassam-Martinez, Javier Martin-Gonzalez, Virginia Pascual-Tejerina, Simon Gundin-Menendez
Publikováno v:
Molecular Biology Reports. 48:1601-1606
Genotyping of ST2 and galectin-3 in atrial fibrillation (AF) is not well analyzed. The aim of our study was to analyze the possible relationship between levels of sST2 and galectin-3 and three polymorphisms in patients with AF. We included 125 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1860b7524041b7fc21dbd86dd18ac2
https://doi.org/10.1007/s11033-021-06150-1
https://doi.org/10.1007/s11033-021-06150-1
Autor:
Ana Merino-Merino, Ruth Saez-Maleta, Ricardo Salgado-Aranda, Daniel AlKassam-Martinez, Virginia Pascual-Tejerina, Javier Martin-Gonzalez, Javier Garcia-Fernandez, Jose-Angel Perez-Rivera
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 9; Pages: 1406
Atrial fibrillation (AF) is explained by anatomical and electrophysiological changes in the atria determined by high pressure, dilatation, infiltration and inflammation in the myocardium. There are some biomarkers implicated in these processes, namel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0845a877dc329a54dd7b790cc34bc63a
https://doi.org/10.3390/jpm12091406
https://doi.org/10.3390/jpm12091406
Autor:
Ricardo Salgado-Aranda, Daniel AlKassam-Martinez, Javier Garcia-Fernandez, Javier Martin-Gonzalez, Jose-Angel Perez-Rivera, Virginia Pascual-Tejerina, Ruth Saez-Maleta, Ana Merino-Merino
Publikováno v:
The American journal of emergency medicine. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a849dda8e2c7a477e88bc1a31f8951
https://pubmed.ncbi.nlm.nih.gov/32487461
https://pubmed.ncbi.nlm.nih.gov/32487461
Autor:
Ignacio Blanco, Enrique Fernández-Bustillo, Daniel Alkassam, Carmen Rodríguez Menéndez, Frederick J. de Serres
Publikováno v:
Medicina Clínica. 123:761-765
Fundamento y objetivo: El deficit de alfa-1-antitripsina (DAAT) es un trastorno hereditario con un riesgo incrementado de padecer enfisema pulmonar y hepatopatias cronicas en ninos y adultos. Actualmente existe en Espana la posibilidad de aplicar tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b24731a24cd94fe1a47845d5b0cdbbd
https://doi.org/10.1016/s0025-7753(04)74661-8
https://doi.org/10.1016/s0025-7753(04)74661-8