Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Paloma Garay-Sánchez"'
Autor:
Nieves Jaén-Sánchez, Gloria González-Azpeitia, Cristina Carranza-Rodriguez, Nicholas Manwere, Paloma Garay-Sánchez, Laura Vallejo-Torres, José-Luis Pérez-Arellano
Publikováno v:
Malaria Journal, Vol 22, Iss 1, Pp 1-8 (2023)
Abstract Background Plasmodium falciparum infection in pregnant women in sub-Saharan Africa is often asymptomatic. As these forms of malaria are often submicroscopic and difficult to diagnose by conventional methods (microscopy and/or rapid diagnosti
Externí odkaz:
https://doaj.org/article/fc853372547447e498b034265efa78d3
Autor:
José María Medina-Gil, Ana Pérez-García, Pedro Saavedra-Santana, Asunción Díaz-Carrasco, Efrén Martínez-Quintana, Fayna Rodríguez-González, Cristina M. Ramírez, Marta Riaño, Paloma Garay-Sánchez, Antonio Tugores
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Monocytes participate in the development of atherosclerosis through the action of cytokines and other inflammatory mediators. Among them, CCR2 and its ligands, CCL2 and CCL7 play an important role, so the main objective of this work was to determine
Externí odkaz:
https://doaj.org/article/c7b07c933f2b40649069f189340042ed
Autor:
Milagros Santana-Verano, Paloma Garay-Sánchez, Francisco Rodriguez-Esparragon, Pascual Lorente-Arencibia, Luis García-Villarreal, Carlos Flores, Juana N. Benitez-Reyes, Fernando Fernández-Fuertes, Antonio Tugores, Luis A. Rubio-Rodríguez, Rafaela González-Montelongo, Tanausú delaCruz
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 74(2)
OBJECTIVES Diagnosis of Wilson disease is difficult and, as early detection may prevent all symptoms, it is essential to know the exact prevalence in order to evaluate the cost- efficacy of a screening program. As the number of WD patients was high i
Autor:
Jesús M González, Daniel González-Santana, Andrea Hernández-Ortega, Marta Riaño, Antonio Tugores, Luis García-Villarreal, Vicente Olmo-Quintana, Paloma Garay-Sánchez, Almudena Sánchez-Villegas, Ildefonso Quiñones, Raquel Moreno-Pérez, Carmen Espinós, Luis Peña-Quintana, Ana Sánchez-Monteagudo, Alberto Monescillo, Teresa Ramírez-Lorenzo
Publikováno v:
JOURNAL OF GASTROENTEROLOGY
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
Background Wilson disease is an autosomal recessive disorder of copper metabolism caused by mutations in the ATP7B gene. An early diagnosis is crucial to prevent evolution of the disease, as implantation of early therapeutic measures fully prevents i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34bdfd0521acfb86647318424f0b5510
https://fundanet.cipf.es/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3595
https://fundanet.cipf.es/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3595
Autor:
Efrén Martínez-Quintana, Paloma Garay-Sánchez, Antonio Tugores, José María Medina-Gil, Marta Riaño, Fayna Rodríguez-González, Pedro Saavedra
Publikováno v:
The Journal of Clinical Pharmacology. 58:1274-1283
Along with aspirin, clopidogrel has been a widely used antiplatelet therapeutic regimen. Although generally well tolerated, its efficacy varies among individuals, with the main hypothesis that its bioavailability relies on its bioconversion to the ac
Autor:
Antonio Tugores, José María Medina-Gil, Paloma Garay-Sánchez, Efrén Martínez-Quintana, Fayna Rodríguez-González
Publikováno v:
Medicina Clínica. 149:235-239
Resumen Introduccion El CYP2C19 es una isoforma del citocromo P450 que metaboliza una serie de farmacos y participa en la sintesis de glucocorticoides. Los polimorfismos del CYP2C19 se han asociado al riesgo genetico de padecer diabetes tipo 2. Metod
Autor:
Antonio Tugores, José María Medina-Gil, Fayna Rodríguez-González, Paloma Garay-Sánchez, Efrén Martínez-Quintana
Publikováno v:
Medicina Clínica (English Edition). 149:235-239
Introduction CYP2C19 is a major isoform of cytochrome P450 that metabolizes a number of drugs and is involved in the glucocorticoids synthesis. CYP2C19 polymorphisms have been associated with the genetic risk for type 2 diabetes. Methods Five hundred
Autor:
Efrén Martínez-Quintana, Fayna Rodríguez-González, Antonio Tugores, Noemí Caballero-Sánchez, Paloma Garay-Sánchez
Publikováno v:
Molecular Syndromology. 8:148-154
Marfan syndrome is an autosomal dominant disorder of the connective tissue caused by mutations in the fibrillin-1 (FBN1) gene. Mutations affecting cysteine residues within the epidermal growith factor-like calcium-binding domains (EGF_CA) of FBN1 are
Autor:
Paloma Garay-Sánchez, Efrén Martínez-Quintana, Antonio Tugores, Fayna Rodríguez-González, José María Medina-Gil
Publikováno v:
Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis. 29(1)
Introduction Paraoxonase 1 (PON1) plays a major role in the oxidation of low density lipoprotein and in the prevention of coronary atherogenesis. In this context, coding region polymorphisms of PON1 gene, responsible for the enzyme activity, has beco
Marfan syndrome is an autosomal dominant disorder of the connective tissue, characterized by early development of thoracic aortic aneurysms and/or dissections, accompanied by ocular and/or skeletal involvement, and is caused by mutations in the fibri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fed3981c01fe5cd4186ba49817cbf0e9
https://europepmc.org/articles/PMC4188161/
https://europepmc.org/articles/PMC4188161/