Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Moises, Selman"'
Autor:
Ana Karem S. Pruneda, José Omar Barreto-Rodríguez, Moises Selman, Fortunato Juárez-Hernández, Ivette Buendía-Roldán
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Since the first case of severe COVID-19, its effect on patients with previous interstitial lung disease (ILD) has been uncertain. We aimed to describe baseline clinical characteristics in ILD patients hospitalized by critical COVI
Externí odkaz:
https://doaj.org/article/a7ac071b2bad4fe08de292478b86f2a8
Autor:
Ata Abbasi, Chixiang Chen, Chintan K. Gandhi, Rongling Wu, Annie Pardo, Moises Selman, Joanna Floros
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Surfactant proteins (SPs) are important for normal lung function and innate immunity of the lungs and their genes have been identified with significant genetic variability. Changes in quantity or quality of SPs due to genetic mutations or natural gen
Externí odkaz:
https://doaj.org/article/9dcf358bef7f4d86a479f974c4dff9e4
Autor:
Ivette Buendia-Roldan, Alexia Palma-Lopez, Danaireth Chan-Padilla, Iliana Herrera, Mariel Maldonado, Rosario Fernández, David Martínez-Briseño, Mayra Mejia, Moises Selman
Publikováno v:
BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Several lung structural and functional abnormalities may occur associated with aging, including emphysema. In this study, we evaluated the frequency and risk factors associated with emphysema in respiratory asymptomatic individual
Externí odkaz:
https://doaj.org/article/cbd0262e81994c1bb3d59e6a28480931
Autor:
Ivette Buendia-Roldan, Marco Antonio Ponce-Gallegos, Daniela Lara-Beltrán, Alma D. Del Ángel-Pablo, Gloria Pérez-Rubio, Mayra Mejía, Moises Selman, Ramcés Falfán-Valencia
Publikováno v:
Biomolecules, Vol 12, Iss 11, p 1662 (2022)
Interstitial lung abnormalities (ILA) are defined as the presence of different patterns of increased lung density, including ground glass attenuation and reticular opacities on chest high-resolution computed tomography (HRCT). In this study, we inclu
Externí odkaz:
https://doaj.org/article/fd16d143d76942f29e5603a21d65ba84
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Hypersensitivity pneumonitis (HP) is one of the most common interstitial lung diseases (ILD), that presents unique challenges for a confident diagnosis and limited therapeutic options. The disease is triggered by exposure to a wide variety of incitin
Externí odkaz:
https://doaj.org/article/ec49eacbeaca4b03bcdcda968aee3389
Autor:
Markus Polke, Yasuhiro Kondoh, Marlies Wijsenbeek, Vincent Cottin, Simon L. F. Walsh, Harold R. Collard, Nazia Chaudhuri, Sergey Avdeev, Jürgen Behr, Gregory Calligaro, Tamera J. Corte, Kevin Flaherty, Manuela Funke-Chambour, Martin Kolb, Johannes Krisam, Toby M. Maher, Maria Molina Molina, Antonio Morais, Catharina C. Moor, Julie Morisset, Carlos Pereira, Silvia Quadrelli, Moises Selman, Argyrios Tzouvelekis, Claudia Valenzuela, Carlo Vancheri, Vanesa Vicens-Zygmunt, Julia Wälscher, Wim Wuyts, Elisabeth Bendstrup, Michael Kreuter
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Background: Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a severe complication associated with a high mortality. However, evidence and guidance on management is sparse. The aim of this international survey was to assess differences
Externí odkaz:
https://doaj.org/article/c21e1f8548a14c949621d342c300cbca
Autor:
Ivette Buendía-Roldan, Rosario Fernández-Plata, Abigail Valdes-Bartolo, Mayra Mejia, Luis E. Jaramillo, David Martínez-Briseño, Armando Santiago-Ruiz, Hugo Tapia-Aguilar, Brenda Gómez-Zamora, Annie Pardo, Moises Selman
Publikováno v:
ERJ Open Research, Vol 6, Iss 3 (2020)
Introduction Phenotypic age better represents age-related biological dysregulation than chronological age. Recently, a multisystem-based ageing measure, which integrates chronological age and nine biomarkers, was proposed. Methods Phenotypic age was
Externí odkaz:
https://doaj.org/article/1e5811cdc8f54fe59c39a04c122c9720
Autor:
Leslie Chavez-Galan, Andy Ruiz, Karen Martinez-Espinosa, Hiram Aguilar-Duran, Martha Torres, Ramces Falfan-Valencia, Gloria Pérez-Rubio, Moises Selman, Ivette Buendia-Roldan
Publikováno v:
Biomolecules, Vol 12, Iss 3, p 445 (2022)
Background: COVID-19 is an infectious disease caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Many COVID-19 patients require invasive mechanical ventilation (IMV) while others, even with acute respiratory failure, do not (
Externí odkaz:
https://doaj.org/article/f6e8640580004c0ba1f9a185cab67034
Autor:
Marc A. Sala, Yalbi Itzel Balderas-Martínez, Ivette Buendía-Roldan, Hiam Abdala-Valencia, Kiwon Nam, Manu Jain, Sangeeta Bhorade, Ankit Bharat, Paul A. Reyfman, Karen M. Ridge, Annie Pardo, Jacob I. Sznajder, G. R. Scott Budinger, Alexander V. Misharin, Moises Selman
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Idiopathic pulmonary fibrosis (IPF) is characterized by progressive scarring of the lung parenchyma, leading to respiratory failure and death. High resolution computed tomography of the chest is often diagnostic for IPF, but its cost and the
Externí odkaz:
https://doaj.org/article/0f2f4f45c02a430d882d843d62500de3
Autor:
Fabián Caro, Ivette Buendía-Roldán, Lorena Noriega-Aguirre, María L. Alberti, Alexandre Amaral, Guillermo Arbo, Santiago Auteri, Aníbal Bermúdez, Pablo Curbelo, Manuel de Jesús Díaz Verduzco, Isabel De la Fuente, Juan I. Enghelmayer, Martin Fernández, Matías Florenzano, Fernando Guillen, Ronaldo Kairalla, Yuri Liberato, Carlos Matiz, Mayra Mejía, Viviana Moyano, Alfredo Pachas, Silvia V. Escotorin, Gabriela Tabaj, Esther Tavera, Alvaro Undurraga, Brenda Varela, José Luis Velazquez, Moises Selman
Publikováno v:
Archivos de Bronconeumología. 58:794-801
Idiopathic pulmonary fibrosis (IPF) is a progressive, irreversible and frequently fatal disease. Currently there are national and multinational registries in Europe, United States, Australia and China to better understand the magnitude of the problem