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7 results on '"Santos-Chávez, Eros"'

3. Genetic, Immunological, and Clinical Features of the First Mexican Cohort of Patients with Chronic Granulomatous Disease

Author

Blancas-Galicia, Lizbeth, Santos-Chávez, Eros, Deswarte, Caroline, Mignac, Quentin, Medina-Vera, Isabel, León-Lara, Ximena, Roynard, Manon, Scheffler-Mendoza, Selma C, Rioja-Valencia, Ricardo, Alvirde-Ayala, Alexandra, Lugo Reyes, Saul O, Staines-Boone, Tamara, García-Campos, Jorge, Saucedo-Ramírez, Omar J, Del-Río_Navarro, Blanca E, Zamora-Chávez, Antonio, López-Larios, Arturo, García-Pavón-Osorio, Susana, Melgoza-Arcos, Eugenia, Canseco-Raymundo, María R, Mogica-Martínez, Dolores, Venancio-Hernández, Marco, Pacheco-Rosas, Daniel, Pedraza-Sánchez, Sigifredo, Guevara-Cruz, Martha, Saracho-Weber, Federico, Gámez-González, Berenise, Wakida-Kuzunoki, Guillermo, Morán-Mendoza, Ana R, Macías-Robles, Ana P, Ramírez-Rivera, Roselia, Vargas-Camaño, Eugenia, Zarate-Hernández, Carmen, Gómez-Tello, Héctor, Ramírez-Sánchez, Emmanuel, Ruíz-Hernández, Fredy, Ramos-López, Domingo, Acuña-Martínez, Héctor, García-Cruz, María L, Román-Jiménez, María G, González-Villarreal, Marina G, Álvarez-Cardona, Aristóteles, Llamas-Guillén, Beatriz A, Cuellar-Rodríguez, Jennifer, Olaya-Vargas, Alberto, Ramírez-Uribe, Nideshda, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Espinosa-Rosales, Francisco J, Serafín-López, Jeanet, Yamazaki-Nakashimada, Marco, Espinosa-Padilla, Sara, and Bustamante, Jacinta

Published
2020
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6. Enfermedad granulomatosa crónica. Actualización y revisión.

Author

López-Hernández, Itzel, Suárez-Gutiérrez, Marcos, Santos-Chávez, Eros Efraín, Espinosa, Sara, and Blancas-Galicia, Lizbeth

Abstract

Copyright of Revista Alergia de Mexico is the property of Coleg. Mexicano de Inmunologia Clinica y Alergia A.C.; Soc. Lat. de Alergia, Asma e Inmunologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2019
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7. [Chronic granulomatous disease. Update and review].

Author

López-Hernández I, Suárez-Gutiérrez M, Santos-Chávez EE, Espinosa S, and Blancas-Galicia L

Subjects
Humans, Granulomatous Disease, Chronic diagnosis, Granulomatous Disease, Chronic therapy
Abstract

Chronic granulomatous disease (CGD) is a primary immunodeficiency syndrome which is characterized by increased susceptibility to severe fungal and bacterial infections. CGD is the result of the lack of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase enzyme in the patient's phagocytes to produce superoxide. It is characterized by recurrent infections with a narrow spectrum of bacteria and fungi, as well as a common set of inflammatory complications, including inflammatory bowel disease. The most frequently found pathogens are Staphylococcus aureus, species of Aspergillus, species of Klebsiella, Burkholderia cepacia, Serratia marcescens and species of Salmonella. Long term antibiotic prophylaxis has helped fight infections associated with chronic granulomatous disease, while the steady progress in bone marrow transplants and the possibility of gene therapy are defined as permanent treatment options.

Published
2019
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