Zobrazeno 1 - 7
of 7
pro vyhledávání: '"María Fernanda Reina Ávila"'
Autor:
Diego Alejandro Lozano-Espinosa, Germán Camacho-Moreno, Juan Francisco López-Cubillos, Adriana Soraya Díaz-Maldonado, Oscar Javier León-Guerra, Diego Mauricio Galvis-Trujillo, Roy Sanguino-Lobo, Oscar Guillermo Arévalo-Leal, Ana María Eraso-Díaz del Castillo, María Fernanda Reina-Ávila, Vicky Carolina Cárdenas-Hernández, Gabriela Ivankovich-Escoto, Adriana H Tremoulet, Rolando Ulloa-Gutiérrez
Publikováno v:
Revista Paulista de Pediatria, Vol 41 (2022)
Abstract Objective: This study aimed to describe the clinical characteristics and the different phenotypes of children with multisystem inflammatory syndrome in children (MIS-C) temporally related to COVID-19 and to evaluate the risk conditions that
Externí odkaz:
https://doaj.org/article/ced1b1418ef244ce8a082a517eb63b4d
Autor:
Diego Alejandro Lozano-Espinosa, Germán Camacho-Moreno, Juan Francisco López-Cubillos, Adriana Soraya Díaz-Maldonado, Oscar Javier León-Guerra, Diego Mauricio Galvis-Trujillo, Roy Sanguino-Lobo, Oscar Guillermo Arévalo-Leal, Ana María Eraso-Díaz del Castillo, María Fernanda Reina-Ávila, Vicky Carolina Cárdenas-Hernández, Gabriela Ivankovich-Escoto, Adriana H Tremoulet, Rolando Ulloa-Gutiérrez
Publikováno v:
Revista Paulista de Pediatria v.41 2023
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Objective: This study aimed to describe the clinical characteristics and the different phenotypes of children with multisystem inflammatory syndrome in children (MIS-C) temporally related to COVID-19 and to evaluate the risk conditions that favored a
Autor:
Pilar del Rosario Guarnizo Zuccardi, Lyda Rengifo, Lina María Saza Mejía, María Fernanda Reina Ávila, Sandra Patricia Garcés Sterling
Publikováno v:
Revista Colombiana de Reumatología (English Edition). 27:190-201
Hematological alterations are common in patients with systemic lupus erythematosus (SLE). These hematological manifestations may be expressed related to the involvement of cells affected and coagulation changes. The compromise in coagulation is assoc
Publikováno v:
Revista Colombiana de Reumatología (English Edition). 27:26-36
Background Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in the paediatric age. It is estimated that between 30–60% of adults patients persist with active disease, which leads to sequelae and complications as well as a de
Publikováno v:
Revista Colombiana de Reumatología, Volume: 27, Issue: 1, Pages: 26-36, Published: 13 DEC 2020
Background: Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in the paediatric age. It is estimated that between 30-60% of adults patients persist with active disease, which leads to sequelae and complications as well as a dec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39bf1165ae3279540ce5ee68e8765a9
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-81232020000100026&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-81232020000100026&lng=en&tlng=en
Autor:
Pilar del Rosario Guarnizo Zuccardi, Lina María Saza Mejía, María Fernanda Reina Ávila, Sandra Patricia Garcés Sterling, Lyda Rengifo
Publikováno v:
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Haematological alterations are common in patients with systemic lupus erythematosus (SLE). These haematological manifestations may be expressed related to the involvement of cells affected and coagulation changes. The compromise in coagulation is ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb034ef0c7055e3d503b8f2454033365
https://repository.urosario.edu.co/handle/10336/23063
https://repository.urosario.edu.co/handle/10336/23063
Autor:
Richard Baquero Rodriguez, Ana Katherina Serrano Gayubo, Juan Carlos Prieto Rivera, Juan Guillermo Cardenas Aguilera, Carmen Inés Rodríguez Cuéllar, Maria Fernanda Reina Ávila, Mayra Alexandra Estévez Capacho, Heidy Mateus, Maylin Valencia González, Kelly Rocío Chacón Acevedo, Maria Paula Gutiérrez Sepúlveda, Dominique P Germain, Juan Politei, Alejandro Fabian Fainboim, Magdalena Cerón Rodríguez, Gustavo Cabrera, Edicson Rodríguez Ibarra, Martha Isabel Carrascal Guzmán, Lida Esperanza Martínez Cáceres, Sandra Yaneth Ospina Lagos, Hernán Trimarchi, Miguel Liern
Publikováno v:
Revista Ciencias de la Salud, Vol 21, Iss 3 (2023)
Antecedentes: La enfermedad de Fabry (EF) es una enfermedad rara ligada a X secundaria al depósito lisosomal de glicoesfingolípidos debido a la deficiencia de la enzima alfa galactosidasa A (α-Gal A). A pesar de su baja frecuencia, es una condici
Externí odkaz:
https://doaj.org/article/af4409f518254bde91f5bf4071f9aac5