Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Aidé Tamara Staines‑Boone"'
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
Autor:
Tábata Takahashi França, Lucila Akune Barreiros, Ranieri Coelho Salgado, Sarah Maria da Silva Napoleão, Lillian Nunes Gomes, Janáira Fernandes Severo Ferreira, Carolina Prando, Cristina Worm Weber, Regina Sumiko Watanabe Di Gesu, Cecilia Montenegro, Carolina Sanchez Aranda, Gisele Kuntze, Aidé Tamara Staines-Boone, Edna Venegas-Montoya, Juan Carlos Aldave Becerra, Liliana Bezrodnik, Daniela Di Giovanni, Ileana Moreira, Gisela Analia Seminario, Andrea Cecilia Gómez Raccio, Mayra de Barros Dorna, Nelson Augusto Rosário-Filho, Herberto Jose Chong-Neto, Elisa de Carvalho, Milena Baptistella Grotta, Julio Cesar Orellana, Miguel Garcia Dominguez, Oscar Porras, Laura Sasia, Karina Salvucci, Emilio Garip, Luiz Fernando Bacarini Leite, Wilma Carvalho Neves Forte, Fernanda Pinto-Mariz, Ekaterini Goudouris, María Enriqueta Nuñez Nuñez, Magdalena Schelotto, Laura Berrón Ruiz, Diana Inés Liberatore, Hans D. Ochs, Otavio Cabral-Marques, Antonio Condino-Neto
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
CD40 ligand (CD40L) deficiency is a rare inborn error of immunity presenting with heterogeneous clinical manifestations. While a detailed characterization of patients affected by CD40L deficiency is essential to an accurate diagnosis and management,
Autor:
Estefanía Vásquez-Echeverri, Marco Antonio Yamazaki-Nakashimada, Edna Venegas Montoya, Selma Cecilia Scheffler Mendoza, Lina Maria Castano-Jaramillo, Edgar Alejandro Medina-Torres, Maria Edith González-Serrano, Melissa Espinosa-Navarro, Juan Carlos Bustamante Ogando, María Guadalupe González-Villarreal, Margarita Ortega Cisneros, Pedro Francisco Valencia Mayoral, Alejandra Consuelo Sanchez, Gustavo Varela-Fascinetto, Rosa María Nideshda Ramírez-Uribe, Yuridia Salazar Gálvez, Laura Cecilia Bonifaz Alonzo, Ezequiel Moisés Fuentes-Pananá, Noemí Gómez Hernández, César Mauricio Rojas Maruri, Jean-Laurent Casanova, Sara Elva Espinosa-Padilla, Aidé Tamara Staines Boone, Gabriel López-Velázquez, Bertrand Boisson, Saul Oswaldo Lugo Reyes
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 11:1261-1280.e8
Autor:
Aidé Tamara Staines‐Boone, María Guadalupe González‐Villareal, María Teresa Pompa‐Garza, Teodoro Muñiz‐Ronquillo, Adriana Carolina Sandoval‐González, David Muzquiz‐Zermeño, Marco Antonio Padilla‐Castro, Jorge Alberto García‐Campos, Luz María Sánchez‐Sánchez, Edna Venegas Montoya, Saul O. Lugo Reyes
Publikováno v:
Scandinavian Journal of Immunology. 95
For many patients with primary immune deficiency (PID), stem-cell transplantation (SCT) may be life-saving.To review our experience of 11 years transplanting children with PID in Mexico.Chart review of patients who underwent SCT from 2008 to 2018, to
Autor:
Tábata Takahashi França, Lucila Akune Barreiros, Ranieri Coelho Salgado, Sarah Maria da Silva Napoleão, Lillian Nunes Gomes, Janáira Fernandes Severo Ferreira, Carolina Prando, Cristina Worm Weber, Regina Sumiko Watanabe Di Gesu, Cecilia Montenegro, Carolina Sanchez Aranda, Gisele Kuntze, Aidé Tamara Staines‑Boone, Edna Venegas‑Montoya, Juan Carlos Aldave Becerra, Liliana Bezrodnik, Daniela Di Giovanni, Ileana Moreira, Gisela Analia Seminario, Andrea Cecilia Gómez Raccio, Mayra de barros Dorna, Nelson Augusto Rosario‑Filho, Herberto Jose Chong‑Neto, Elisa de Carvalho, Milena Baptistella Grotta, Julio Cesar Orellana, Miguel Garcia Dominguez, Oscar Porras, Laura Sasia, Karina Salvucci, Emilio Garip, Luiz Fernando Bacarini Leite, Wilma Carvalho Neves Forte, Fernanda Pinto‑Mariz, Ekaterini Goudouris, María Enriqueta Nuñez Nuñez, Magdalena Schelotto, Laura Berrón Ruiz, Diana Inés Liberatore, Hans D. Ochs, Otavio Cabral‑Marques, Antonio Condino‑Neto
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Autor:
María Edith González-Serrano, Edna Venegas-Montoya, Saul Oswaldo Lugo Reyes, David Múzquiz-Zermeño, Yuridia Salazar-Galvez, Rubén Antonio Córdova-Gurrola, Luz María Sánchez-Sánchez, Jorge García-Campos, Aidé Tamara Staines-Boone
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
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
Autor:
Edgar Alejandro Medina Torres, Lizbeth Blancas Galicia, Selma Cecilia Scheffler Mendoza, Saul Oswaldo Lugo Reyes, Aidé Tamara Staines-Boone, Nora Hilda Segura Méndez, Estefanía Vásquez-Echeverri, Edna Venegas Montoya, Juan Carlos Bustamante Ogando, Luisa B Gámez González, Jesús Moisés Ramírez López, Lina María Castaño-Jaramillo, Gabriela López-Herrera, Sara Elva Espinosa-Padilla, David Muzquiz Zermeño, Patricia María O’Farrill-Romanillos, Marco Antonio Yamazaki-Nakashimada, Luz María Sánchez-Sánchez, Jorge Alberto García Campos, Laura Berron Ruiz
Publikováno v:
Journal of Clinical Immunology
Introduction Patients with inborn errors of immunity (IEI) have a compromised or inappropriate immune response. Although they might be considered a high-risk group for severe SARS-CoV-2 infection, the reported impact of COVID-19 in these patients has
Autor:
Selma Scheffler-Mendoza, Edna Venegas-Montoya, Jorge Yáñez, Julie E. Niemela, Iván Martínez-Duncker, Guillermo Wakida, Karol Carrillo-Sánchez, Laura Berrón-Ruiz, Saúl Oswaldo Lugo-Reyes, Carolina Molina-Garay, Luigi D. Notarangelo, Mario E Cruz-Muñoz, Nina Pastor, Carmen Alaez-Verson, Aidé Tamara Staines-Boone, Paul Gaytán, Sara Elva Espinosa-Padilla, Marco Antonio Yamazaki-Nakashimada, Maria Enriqueta Nuñez-Nuñez, Luis Leonardo Flores-Lagunes, Edith González-Serrano, Ana Paola Macías-Robles, Sergio D. Rosenzweig
Publikováno v:
J Clin Immunol
Mutations in Recombinase Activating Genes 1 and 2 (RAG1/2) results in human severe combined immunodeficiency (SCID). The products of these genes, are essential for V(D)J rearrangement of the antigen receptors during lymphocyte development. Nonsense m