Výsledky vyhledávání - "Edwin Pardo-Díaz"

Use of Infliximab in the Treatment of Macrophage Activation Syndrome Complicating Kawasaki Disease

Autor: Marco Antonio Yamazaki-Nakashimada, Luis Martín Garrido-García, Edwin Pardo-Díaz, Marco A Ruiz-Ontiveros, Andrea Iglesias-Amaya, Selma Scheffler-Mendoza, Leonardo Rivera-Rodríguez, Sarbelio Moreno-Espinosa

Publikováno v: Journal of Pediatric Hematology/Oncology. 43:e448-e451

Kawasaki disease (KD) is an acute systemic vasculitis of unknown etiology. KD can be complicated with macrophage activation syndrome. The optimal treatment for this KD complication has not been established, and a variety of treatments have been used.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d6371887e2082ddfed57182c72a4e2c
https://doi.org/10.1097/mph.0000000000001756

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Juvenile Dermatomyositis Triggered by SARS-CoV-2

Autor: Beatriz Bayardo-Gutierrez, Eduardo Liquidano-Perez, Marian Kristalia Rivas-Calderón, Mariana Maza-Morales, Marco Antonio Yamazaki-Nakashimada, Edwin Pardo-Díaz, Selma Scheffler-Mendoza, María Teresa García-Romero

Publikováno v: Pediatric Neurology. 121:26-27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b965a258bee9b6bb9c34d71ffbb524fc
https://doi.org/10.1016/j.pediatrneurol.2021.05.011

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MANEJO DE LA VÍA AÉREA PEDIÁTRICA

Autor: Alejandra Jiménez Hernández, Edwin Pardo Díaz

Publikováno v: GastrohNup. 17

Para entender, diagnosticar y tratar las condiciones patológicas propias de la vía aérea del niño, es necesario un adecuado conocimiento de su anatomía y fisiología. La vía aérea del adulto es completamente diferente a la del niño, haciendo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8812149c9b81d2623338177f567d4f2d
https://doi.org/10.25100/gnup.v17i3s3.1377

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Analyses of the PRF1 Gene in Individuals with Hemophagocytic Lymphohystiocytosis Reveal the Common Haplotype R54C/A91V in Colombian Unrelated Families Associated with Late Onset Disease

Autor: Lucía Carolina Leal-Esteban, Jack J. Bleesing, Yadira Coll, Yolanda Caicedo, Claudia M. Trujillo-Vargas, José Luis Franco, Isaura Pilar Sánchez, Julio César Orrego, Jacques Zimmer, Jesús A. Álvarez-Álvarez, Malyive L. Serna, Camilo A. Perez-Romero, Edwin Pardo-Díaz

Publikováno v: Journal of Clinical Immunology. 32:670-680

Familial hemophagocytic lymphohistiocytosis (FHL), is a rare autosomal recessive disorder characterized by an impairment of cytotoxic cells and uncontrolled activation of macrophages. This study presents the first description of four patients with FH

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91b662b30c9bfff44a9fb0c7d3ed514d
https://doi.org/10.1007/s10875-012-9680-5

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