Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Antonio Ferreira Cerdán"'
Autor:
Rebeca Rodríguez-Pena, Elena Pérez-Costa, María José Mellado, Eduardo López-Granados, Ana Méndez-Echevarría, Alejandro Zarauza, Antonio Ferreira-Cerdán, Teresa Del Rosal, Maria Bravo
Publikováno v:
Pediatric Infectious Disease Journal. 35:794-798
Background: Survival of children with combined immunodeficiency is strongly related to patient’s age and clinical situation at the time of hematopoietic stem cell transplantation (HSCT). We describe the clinical features before HSCT or enzyme repla
Autor:
Julián Nevado, Antonio Ferreira Cerdán, Ana Sastre Urgelles, María Bravo García-Morato, Rebeca Rodríguez Pena, Luis Ignacio Gonzalez-Granado
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice. 5:1146-1148
Autor:
Marian Davila, Jean-Laurent Casanova, Antonio Ferreira Cerdán, Carolina Cubillos-Zapata, Juan Torres, Rubén Martínez-Barricarte, Victor Toledano, Sonia García-Gómez, Rebeca Pérez de Diego, Enrique Hernández-Jiménez, María Teresa Vallejo-Cremades, Eduardo López-Collazo, Rita Álvarez Doforno, Silvia Sánchez-Ramón, Miguel Fernández Arquero
Publikováno v:
Clinical immunology (Orlando, Fla.). 163
B-cell lymphoma 10 (BCL10) is not essential for actin polymerisation after FcγR stimulation in human fibroblasts.
Autor:
Ana V. Marin, José R. Regueiro, María Merino, Angel L. Corbí, María Coronel Díaz, Rebeca Rodríguez Pena, Anaïs Jiménez-Reinoso, Francisco Javier Aracil Santos, Elena Vallespín García, Diego Plaza Lopez de Sabando, Hugh T. Reyburn, Juan Torres Canizales, Mar Valés-Gómez, Ernesto Roldán Santiago, Raúl de Lucas-Laguna, Laura Casamayor Polo, Ángeles Domínguez-Soto, Alfonso Blázquez Moreno, María Bravo García-Morato, Paula P. Cárdenas, Yasmina Mozo del Castillo, Eduardo López-Granados, Francisco José Sanz Santaeufemia, Lucía del Pino Molina, Ángela del Pozo Maté, Antonio Ferreira Cerdán, Julián Nevado Blanco, Marta Feito Rodríguez, Alejandro C. Briones
Publikováno v:
Journal of Allergy and Clinical Immunology. 141:1924-1927.e18
Autor:
Jean-Laurent Casanova, Antonio Ferreira Cerdán, Rubén Martínez-Barricarte, Anne Puel, Carolina Cubillos-Zapata, Rebeca Pérez de Diego, Silvia Sánchez-Ramón, Eduardo López-Collazo
Publikováno v:
The Journal of allergy and clinical immunology. 136(5)
Three members of the caspase recruitment domain (CARD) family of adaptors (CARD9, CARD10, and CARD11) are known to form heterotrimers with B-cell lymphoma 10 (BCL10) and mucosa-associated lymphoid tissue lymphoma-translocation gene 1 (MALT1). These 3
Autor:
María Cruz Rodríguez, Rebeca Pérez de Diego, Gumersindo Fontán Casariego, Antonio Ferreira Cerdán, Eduardo López-Granados
Publikováno v:
The Journal of allergy and clinical immunology. 116(3)
Background X-linked (Bruton's) agammaglobulinemia (XLA) is a rare immunodeficiency caused by a block in B-cell development caused by mutations in the Bruton's tyrosine kinase (BTK) gene. Many aspects of XLA and BTK function remain unresolved; atypica
Publikováno v:
Clinical Immunology. 145:59-60
Autor:
Gumersindo Fontán Casariego, Antonio Ferreira Cerdán, Eduardo López Granados, M. Cruz Garcia Rodriguez, Rebeca Pérez de Diego
Publikováno v:
Journal of Allergy and Clinical Immunology. 115:205-206
Autor:
Antonio Ferreira-Cerdán, Gumersindo Fontán, Javier Arpa, Margarita López-Trascasa, Isabel M. Ponce, Carolina González-Rubio
Publikováno v:
Archives of Neurology. 58:1923
Background Complement (C) factor I deficiency is a rare immunodeficiency state frequently associated with recurrent pyogenic infections in early infancy. This deficiency causes a permanent uncontrolled activation of the alternative pathway resulting
Autor:
Ma Cruz García Rodríguez, Antonio Ferreira Cerdán, Gumersindo Fontán Casariego, Eduardo López Granados
Publikováno v:
Human Mutation. 18:84-84
Mutations in Bruton’s tyrosine kinase (BTK) gene result in X linked agammaglobulinemia (XLA). Using Single Strand Conformation Polymorphism (SSCP) followed by direct sequencing 21 mutations were found in 27 patients with an XLA phenotype from 21 un