Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Julio Sandoval Zárate"'
Autor:
María Luna-Luna, David Cruz-Robles, Nydia Ávila-Vanzzini, Valentín Herrera-Alarcón, Jesús Martínez-Reding, Sergio Criales-Vera, Julio Sandoval-Zárate, Jesús Vargas-Barrón, Carlos Martínez-Sánchez, Armando Roberto Tovar-Palacio, José Manuel Fragoso, Elizabeth Carreón-Torres, Gilberto Vargas-Alarcón, Óscar Pérez-Méndez
Publikováno v:
Lipids in Health and Disease, Vol 16, Iss 1, Pp 1-8 (2017)
Abstract Background Previous studies suggest a relationship of the epicardial adipose tissue (EAT) with progression and calcification of the atherosclerotic plaque; however, it is unknown if this tissue expresses genes that may participate on these p
Externí odkaz:
https://doaj.org/article/5290c393333f4e3fa162bc5d1e349ee0
Autor:
Carlos Jerjes-Sánchez, Rodolfo Parra Michel, Francisco Moreno Hoyos Abril, Julio Sandoval Zárate, Mario Seoane García de León, José Javier Elizalde González, Humberto Garcia Aguilar, Tomás Pulido Zamudio, Pedro Gutiérrez-Fajardo, Alicia Ramirez-Rivera, Miguel Beltran Gamez
Publikováno v:
Archivos de Cardiología de México. 87:13-17
Objetivo: REMEHIP es un registro prospectivo, multicentrico en hipertension pulmonar. El objetivo principal sera identificar el perfil clinico, atencion medica, tendencias terapeuticas y evolucion en pacientes mexicanos adultos y pediatricos con hipe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bc30f6a264475c70332fb3f58e7a3d3
https://doi.org/10.1016/j.acmx.2016.11.006
https://doi.org/10.1016/j.acmx.2016.11.006
Publikováno v:
Archivos de Cardiología de México. 87:26-34
Chronic thromboembolic pulmonary hypertension (CTEPH) represents a unique subtype of pulmonary hypertension characterized by the presence of mechanical obstruction of the major pulmonary vessels caused by venous thromboembolism. CTEPH is a progressiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30c0500b20b0c9a6d5e81477d14a676
https://doi.org/10.1016/j.acmx.2016.10.003
https://doi.org/10.1016/j.acmx.2016.10.003
Autor:
Julio César López-Reyes, Tomas Pulido-Zamudio, Julio Sandoval-Zárate, Nayeli Guadalupe Zayas-Hernandez, Oscar Gabriel Jiménez Cabrera
Publikováno v:
Acute critical care.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c879ef860d6eb9f6161439c31643e433
https://doi.org/10.1183/13993003.congress-2019.pa2285
https://doi.org/10.1183/13993003.congress-2019.pa2285
Autor:
Julio Sandoval Zárate, Tomás Pulido Zamudio, Carlos Sisniega, Nayeli Zayas Hernadnez, Ricardo Teijeiro Paradis, Leonardo del Valle, Felipe Massó, Gustavo Pastelín, Hector Gonzalez
Publikováno v:
Pulmonary hypertension.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b37a0e5d2a5b427f3008316340217060
https://doi.org/10.1183/13993003.congress-2018.pa3047
https://doi.org/10.1183/13993003.congress-2018.pa3047
Publikováno v:
Archivos de Cardiología de México. 85:215-224
In experimental and clinical cardiology, phosphodiesterase type 5 (PDE-5) inhibitors have brought scientific interest as a therapeutic tool in pulmonary arterial hypertension (PAH) management in recent years. Phosphodiesterases are a superfamily of e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::906015c8778957b361022b2410bba8ad
https://doi.org/10.1016/j.acmx.2015.03.001
https://doi.org/10.1016/j.acmx.2015.03.001
Publikováno v:
Archivos de Cardiología de México. 85:32-49
Pulmonary arterial hypertension is a common complication of congenital heart disease (CHD). Congenital cardiopathies are the most frequent congenital malformations. The prevalence in our country remains unknown, based on birthrate, it is calculated t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dfb8c20faca2e26f22c59a04d90713d
https://doi.org/10.1016/j.acmx.2014.11.008
https://doi.org/10.1016/j.acmx.2014.11.008
Publikováno v:
Archivos de cardiologia de Mexico. 87(1)
Chronic thromboembolic pulmonary hypertension (CTEPH) represents a unique subtype of pulmonary hypertension characterized by the presence of mechanical obstruction of the major pulmonary vessels caused by venous thromboembolism. CTEPH is a progressiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1901f03be21255e235aaebef960c392a
https://pubmed.ncbi.nlm.nih.gov/27956338
https://pubmed.ncbi.nlm.nih.gov/27956338
Publikováno v:
Archivos de cardiologia de Mexico. 85(3)
In experimental and clinical cardiology, phosphodiesterase type 5 (PDE-5) inhibitors have brought scientific interest as a therapeutic tool in pulmonary arterial hypertension (PAH) management in recent years. Phosphodiesterases are a superfamily of e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8485873ffc84888d6ec9820c2b918ab1
https://pubmed.ncbi.nlm.nih.gov/26047999
https://pubmed.ncbi.nlm.nih.gov/26047999
Publikováno v:
Archivos de cardiologia de Mexico. 85(1)
Pulmonary arterial hypertension is a common complication of congenital heart disease (CHD). Congenital cardiopathies are the most frequent congenital malformations. The prevalence in our country remains unknown, based on birthrate, it is calculated t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8e413b464f2670c877e1455d5f7e91b
https://pubmed.ncbi.nlm.nih.gov/25650280
https://pubmed.ncbi.nlm.nih.gov/25650280