Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aristóteles Álvarez-Cardona"'
Autor:
Alejandro Tarango-García, Silvia Rodríguez-Narciso, Netzahualcóyotl Castañeda-Leyva, Hannia M. Prieto-Nevárez, Saul O. Lugo Reyes, Francisco J. Espinosa-Rosales, Sara Elva Espinosa-Padilla, Aidé T. Staines-Boone, Luis F. Torres-Bernal, Aristóteles Álvarez-Cardona
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
PurposeImmunoglobulin replacement therapy remains a cornerstone of treatment in antibody deficiencies and other inborn errors of immunity. While patient preferences between subcutaneous and intravenous immunoglobulin have been studied through questio
Externí odkaz:
https://doaj.org/article/6863d3b3930f4d35a89dfaa3c2bc73bb
Autor:
Marcos Suárez-Gutiérrez, Jorge Eduardo Macías-Garza, Daniela Jazmín López-Ortiz, Brenda Fuentes, Aristóteles Álvarez-Cardona
Publikováno v:
Revista Alergia México, Vol 66, Iss 4, Pp 388-393 (2019)
Background: Allergic rhinitis is the most common allergic disease worldwide and it is caused by a reaction of hypersensitivity to aeroallergens. To our knowledge, there aren’t any previous studies of aeroallergenic sensitization in Aguascalientes,
Externí odkaz:
https://doaj.org/article/0070d6334f9f40aa974b87a1297df967
Autor:
Marcos Suárez-Gutiérrez, Marco Antonio Yamazaki-Nakashimada, Sara Espinosa, Lizbeth Blancas-Galicia, Saúl Oswaldo Lugo-Reyes, Aristóteles Álvarez-Cardona
Publikováno v:
Revista Alergia México, Vol 66, Iss 4, Pp 456-473 (2019)
The autoimmune lymphoproliferative syndrome (ALPS) is an inborn immunity error, which is the result of a heterogeneous group of mutations in the genes that regulate the apoptosis phenomenon. It typically appears in the first years of life. The most c
Externí odkaz:
https://doaj.org/article/329488ddf65a49de9154bd4a6b89afaf
Autor:
Patricia Baeza Capetillo, Natalia Velez-Tirado, Kaan Boztug, Sara Elva Espinosa-Padilla, Genny M Chaia Semerena, Tatjana Hirschmugl, Saul Oswaldo Lugo Reyes, Aristóteles Álvarez-Cardona, Enrique Lopez Valentín, Selma Scheffler-Mendoza, Christoph Klein, Wojciech Garncarz, Armando Partida-Gaytán, Jesús Aguirre Hernández, Marcos Alejandro Suárez Gutiérrez, Edgar Alejandro Medina-Torres, Marco Antonio Yamazaki-Nakashimada
Glucose-6-phosphate catalytic subunit 3 (G6PC3) deficiency is characterized by severe congenital neutropenia with recurrent pyogenic infections, a prominent superficial venous pattern and cardiovascular and urogenital malformations caused by an alter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0213fa74f15334d9458a368d24974577
https://doi.org/10.21203/rs.3.rs-356870/v2
https://doi.org/10.21203/rs.3.rs-356870/v2
Autor:
Sara Espinosa, Saúl Oswaldo Lugo-Reyes, Lizbeth Blancas-Galicia, Aristóteles Álvarez-Cardona, Marcos Suárez-Gutiérrez, Marco Antonio Yamazaki-Nakashimada
Publikováno v:
Revista Alergia México. 66:456-473
El síndrome linfoproliferativo autoinmune (ALPS, autoimmune lymphoproliferative syndrome) es un error innato de la inmunidad, resultado de un grupo heterogéneo de alteraciones en los genes que regulan el fenómeno de apoptosis. Se manifiesta típic
Publikováno v:
Journal of the Selva Andina Research Society. 10:52-61
Autor:
Marcos Suárez-Gutiérrez, Marco Antonio Yamazaki-Nakashimada, Sara Espinosa, Lizbeth Blancas-Galicia, Saúl Oswaldo Lugo-Reyes, Aristóteles Álvarez-Cardona
Publikováno v:
Revista Alergia México, Vol 66, Iss 4, Pp 456-473 (2019)
The autoimmune lymphoproliferative syndrome (ALPS) is an inborn immunity error, which is the result of a heterogeneous group of mutations in the genes that regulate the apoptosis phenomenon. It typically appears in the first years of life. The most c
Autor:
Marco Venancio-Hernández, Jorge García-Campos, Alberto Olaya-Vargas, Alexandra Alvirde-Ayala, Martha Guevara-Cruz, Emmanuel Ramírez-Sánchez, Héctor Acuña-Martínez, Ana R Morán-Mendoza, Manon Roynard, María R Canseco-Raymundo, Selma Scheffler-Mendoza, Dolores Mogica-Martínez, Ximena León-Lara, Stéphanie Boisson-Dupuis, Eugenia Melgoza-Arcos, Domingo Ramos-López, Jennifer Cuellar-Rodríguez, Federico Saracho-Weber, Lizbeth Blancas-Galicia, Roselia Ramírez-Rivera, Francisco J. Espinosa-Rosales, Jeanet Serafín-López, Berenise Gámez-González, Arturo López-Larios, Marco Antonio Yamazaki-Nakashimada, Aristóteles Álvarez-Cardona, Daniel Pacheco-Rosas, Isabel Medina-Vera, Quentin Mignac, María de la Luz Hortensia García-Cruz, Susana García-Pavón-Osorio, T. Staines-Boone, Héctor Gómez-Tello, Omar J Saucedo-Ramírez, Fredy Ruíz-Hernández, Sara Elva Espinosa-Padilla, Eros Santos-Chávez, Antonio Zamora-Chávez, Nideshda Ramírez-Uribe, Ana Paola Macías-Robles, Eugenia Vargas-Camaño, Caroline Deswarte, Ricardo Rioja-Valencia, Jean-Laurent Casanova, Beatriz A Llamas-Guillén, Blanca E Del-Río Navarro, Saul Oswaldo Lugo Reyes, Marina G González-Villarreal, Jacinta Bustamante, Sigifredo Pedraza-Sánchez, María G Román-Jiménez, Guillermo Wakida-Kuzunoki, Carmen Zarate-Hernández
Publikováno v:
Journal of clinical immunology. 40(3)
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by an inability of phagocytes to produce reactive oxygen species, impairing their killing of various bacteria and fungi. We summarize here the 93 cases of CGD diagnosed i
Autor:
Aristóteles Álvarez-Cardona, Lucila Martínez-Medina, Francisco J. Espinosa-Rosales, Alma R De Luna-Sosa, Alberto Santillan-Artolozaga, Saul Oswaldo Lugo Reyes, Luis Fernando Torres-Bernal, Jaime Asael Lopez-Valdez, Javier Ventura-Juárez, Sara Elva Espinosa-Padilla, Adriana Cajero-Avelar
Publikováno v:
Journal of Clinical Immunology. 36:173-178
Primary immunodeficiencies (PIDs) are a heterogeneous group of disorders characterized mainly by recurrent infections. Late diagnosis remains as one of the main issues to solve. We aimed to increase PID diagnosis in Aguascalientes, a 1.3 million inha
Autor:
Francisco Rivas-Larrauri, Marco Antonio Yamazaki-Nakashimada, Aristóteles Álvarez-Cardona, Lizbeth Blancas-Galicia, Ana Luisa Rodríguez-Lozano
Publikováno v:
Journal of Clinical Immunology. 32:207-211
Objectives Chronic granulomatous disease is a rare phagocyte disorder characterized by an increased susceptibility to infections and inflammatory complications. We describe two patients with chronic granulomatous disease (CGD) complicated by macropha