Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Aide Tamara Staines-Boone"'
Autor:
Saul Oswaldo Lugo-Reyes, Nina Pastor, Edith González-Serrano, Marco Antonio Yamazaki-Nakashimada, Selma Scheffler-Mendoza, Laura Berron-Ruiz, Guillermo Wakida, Maria Enriqueta Nuñez-Nuñez, Ana Paola Macias-Robles, Aide Tamara Staines-Boone, Edna Venegas-Montoya, Carmen Alaez-Verson, Carolina Molina-Garay, Luis Leonardo Flores-Lagunes, Karol Carrillo-Sanchez, Julie Niemela, Sergio D. Rosenzweig, Paul Gaytan, Jorge A. Yañez, Ivan Martinez-Duncker, Luigi D. Notarangelo, Sara Espinosa-Padilla, Mario Ernesto Cruz-Munoz
Publikováno v:
Journal of Clinical Immunology. 41:1708-1708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a376b081b472f3d00cbd3a72dbc59f38
https://doi.org/10.1007/s10875-021-01075-7
https://doi.org/10.1007/s10875-021-01075-7
Autor:
Edna Venegas-Montoya, Aidé Tamara Staines-Boone, Luz María Sánchez-Sánchez, Jorge Alberto García-Campos, Rubén Antonio Córdova-Gurrola, Yuridia Salazar-Galvez, David Múzquiz-Zermeño, María Edith González-Serrano, Saul O. Lugo Reyes
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Autosomal recessive (AR) DOCK8 deficiency is a well-known actinopathy, a combined primary immune deficiency with impaired actin polymerization that results in altered cell mobility and immune synapse. DOCK8-deficient patients present early in life wi
Externí odkaz:
https://doaj.org/article/5ee181f044a444168ac09db68e076bc9
Autor:
Rodolfo Muriel-Vizcaíno, Gabriela Treviño-Garza, Chiharu Murata, Aidé Tamara Staines-Boone, Marco Antonio Yamazaki-Nakashimada, Sara Elba Espinosa-Padilla, Francisco Javier Espinosa-Rosales
Publikováno v:
Acta Pediátrica de México, Vol 37, Iss 1, Pp 17-25 (2016)
Las inmunodeficiencias primarias son enfermedades genéticas caracterizadas, en la mayoría de los casos, por la predisposición del individuo afectado a infecciones recurrentes o graves con afectación de su calidad de vida. Las más frecuentes son
Externí odkaz:
https://doaj.org/article/5c73cbee1b4f403a9f6a0a1ca150cc76
Autor:
Aidé Tamara Staines-Boone, Caroline Deswarte, Edna Venegas Montoya, Luz María Sánchez-Sánchez, Jorge Alberto García Campos, Teodoro Muñiz-Ronquillo, Jacinta Bustamante, Francisco J. Espinosa-Rosales, Saul Oswaldo Lugo Reyes
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
Mutations in the genes coding for cytokines, receptors, second messengers, and transcription factors of interferon gamma (IFN-γ) immunity cause Mendelian susceptibility to mycobacterial disease (MSMD). We report the case of a 7-year-old male patient
Externí odkaz:
https://doaj.org/article/426e79731b1d4013a46ac6995043d690