Zobrazeno 1 - 10
of 198
pro vyhledávání: '"J. Molano"'
Autor:
F. Juliao-Baños, F. Puentes, R. López, M.A. Saffon, G. Reyes, V. Parra, M.T. Galiano, M. Barraza, J. Molano, E. Álvarez, R. Corrales, L.E. Vargas, F. Gil, P. Álvarez, L. Limas, R. Prieto, P. Yance, F. Díaz, J. Bareño, Fabián Juliao-Baños, Mateo Arrubla, Joselyn Camargo, Fabián Puentes, Lázaro Arango, Rocío López, Rafael García, Belén Mendoza, María A. Saffon, Luis F. Roldan, Julio Zuleta, Gustavo Reyes, Viviana Parra, Cristian Flórez, Edilberto Nuñez, María T. Galiano, Marcos Barraza, Isabel C. Sanchez, Jenny L. Molano, Jorge I. Lizarazo, Iván Cuellar, Eligio Álvarez, Rubén Corrales, Fabio Gil, Luz E. Vargas, Patricia Álvarez, Luis M. Limas, Robín Prieto, Hernán Ballén, Lidsay Delgado, Paola Yance, Felha Díaz
Publikováno v:
Revista de Gastroenterología de México (English Edition), Vol 86, Iss 2, Pp 153-162 (2021)
Aim: To determine the clinical, sociodemographic, and treatment characteristics of inflammatory bowel disease (IBD) in a Colombian population register. Methods: A descriptive, analytic, observational, cross-sectional, multicenter study on patients wi
Externí odkaz:
https://doaj.org/article/ca65fe3024414054b817059542a0bee8
Autor:
I. Vieitez, P. Gallano, L. González-Quereda, S. Borrego, I. Marcos, J.M. Millán, T. Jairo, C. Prior, J. Molano, M.J. Trujillo-Tiebas, J. Gallego-Merlo, M. García-Barcina, M. Fenollar, C. Navarro
Publikováno v:
Neurología, Vol 32, Iss 6, Pp 377-385 (2017)
Resumen: Introducción: La distrofia muscular de Duchenne (DMD) es una enfermedad neuromuscular grave que afecta a uno de cada 3.500 varones nacidos y sigue un patrón de herencia ligada al cromosoma X. En esta enfermedad se observa una ausencia tota
Externí odkaz:
https://doaj.org/article/6a373885e1464775b5cb8004abb9b7cd
Autor:
I. Vieitez, P. Gallano, L. González-Quereda, S. Borrego, I. Marcos, J.M. Millán, T. Jairo, C. Prior, J. Molano, M.J. Trujillo-Tiebas, J. Gallego-Merlo, M. García-Barcina, M. Fenollar, C. Navarro
Publikováno v:
Neurología (English Edition), Vol 32, Iss 6, Pp 377-385 (2017)
Introduction: Duchenne muscular dystrophy (DMD) is a severe X-linked recessive neuromuscular disease that affects one in 3500 live-born males. The total absence of dystrophin observed in DMD patients is generally caused by mutations that disrupt the
Externí odkaz:
https://doaj.org/article/c165828ef0f0497e98f3e7368b7b9071
Autor:
Wilfredo R. Matias, Isabel R. Fulcher, Sara M. Sauer, Cody P. Nolan, Yodeline Guillaume, Jack Zhu, Francisco J. Molano, Elizabeth Uceta, Shannon Collins, Damien M. Slater, Vanessa M. Sánchez, Serina Moheed, Jason B. Harris, Richelle C. Charles, Ryan M. Paxton, Sean F. Gonsalves, Molly F. Franke, Louise C. Ivers
Publikováno v:
Journal of Racial and Ethnic Health Disparities.
Objectives Uncovering and addressing disparities in infectious disease outbreaks require a rapid, methodical understanding of local epidemiology. We conducted a seroprevalence study of SARS-CoV-2 infection in Holyoke, Massachusetts, a majority Hispan
Autor:
Sara Suliman, Wilfredo R. Matias, Isabel R. Fulcher, Francisco J. Molano, Shannon Collins, Elizabeth Uceta, Jack Zhu, Ryan M. Paxton, Sean F. Gonsalves, Maegan V. Harden, Marissa Fisher, Jim Meldrim, Stacey Gabriel, Molly F. Franke, Deborah T. Hung, Sandra C. Smole, Lawrence C. Madoff, Louise C. Ivers
Publikováno v:
Scientific Reports. 12
Point-of-care antigen-detecting rapid diagnostic tests (RDTs) to detect Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) represent a scalable tool for surveillance of active SARS-CoV-2 infections in the population. Data on the performance
Autor:
F. Juliao-Baños, F. Puentes, R. López, M.A. Saffon, G. Reyes, V. Parra, M.T. Galiano, M. Barraza, J. Molano, E. Álvarez, R. Corrales, L.E. Vargas, F. Gil, P. Álvarez, L. Limas, R. Prieto, P. Yance, F. Díaz, J. Bareño, Fabián Juliao-Baños, Mateo Arrubla, Joselyn Camargo, Fabián Puentes, Lázaro Arango, Rocío López, Rafael García, Belén Mendoza, María A. Saffon, Luis F. Roldan, Julio Zuleta, Gustavo Reyes, Viviana Parra, Cristian Flórez, Edilberto Nuñez, María T. Galiano, Marcos Barraza, Isabel C. Sanchez, Jenny L. Molano, Jorge I. Lizarazo, Iván Cuellar, Eligio Álvarez, Rubén Corrales, Fabio Gil, Luz E. Vargas, Patricia Álvarez, Luis M. Limas, Robín Prieto, Hernán Ballén, Lidsay Delgado, Paola Yance, Felha Díaz
Publikováno v:
Revista de Gastroenterología de México. 86:153-162
Resumen Objetivo Determinar las caracteristicas clinicas, sociodemograficas y tratamiento de la EII en un registro de la poblacion colombiana. Metodologia Estudio observacional descriptivo, analitico, multicentrico, de corte transversal de una cohort
Autor:
Damien Slater, Vanessa Sanchez, Shannon Collins, Wilfredo R. Matias, Richelle C. Charles, Elizabeth Uceta, Molly F. Franke, Jack Zhu, Yodeline Guillaume, Jason B. Harris, Cody P Nolan, Ryan M. Paxton, Isabel R. Fulcher, Sean F. Gonsalves, Sara M. Sauer, Francisco J. Molano, Louise C. Ivers, Serina Moheed
BackgroundSeroprevalence studies are important tools to estimate the prevalence of prior or recent SARS-CoV-2 infections, identifying hotspots and high-risk groups and informing public health responses to the COVID-19 pandemic. We conducted a city-le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2831bf77da761b8d8299f8c39236b64b
https://doi.org/10.1101/2021.10.13.21264975
https://doi.org/10.1101/2021.10.13.21264975
Publikováno v:
European Heart Journal. 42
Background Incomplete revascularization versus complete revascularization in patients undergoing percutaneous coronary intervention (PCI) is associated with higher risk of mortality and major adverse cardiac events. Cardiac rehabilitation (CR) is one
Publikováno v:
European Heart Journal. 42
Background Short and medium-term benefits of cardiac rehabilitation (CR) after an acute myocardial infarction (AMI) have been well studied. However, studies on long-term benefits of such programs after percutaneous coronary intervention (PCI) are sca
Publikováno v:
European Heart Journal. 42
Introduction Several studies associate atrial fibrillation (AF) presence with a poor prognosis and quality of life in hypertrophic cardiomyopathy (HCM) patients. Detecting and treating AF in time prevents important comorbidities and fatal events as i