Navegar por autor "Lourés Fraga, Esther"

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A novel mutation in ADAMTS13 of a child with Upshaw-Schulman Syndrome

2014- López Fernández, María Fernanda; Batlle Fonrodona, Francisco Javier; Perez Rodriguez, Almudena; Lourés Fraga, Esther; Rodríguez Trillo, Angela; [et al.]
Acquired von Willebrand syndrome and mitral valve prosthesis leakage. A pilot study

2011- Cuenca Castillo, Jose Joaquin; López Fernández, María Fernanda; Batlle Fonrodona, Francisco Javier; Costa Pinto Prego de Faria, María Joana; Perez Rodriguez, Almudena; [et al.]
Diagnosis and management of von Willebrand disease in Spain

2011- López Fernández, María Fernanda; Batlle Fonrodona, Francisco Javier; Perez Rodriguez, Almudena; Lourés Fraga, Esther; Rodríguez Trillo, Angela [et al.]
Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review

2014- López Fernández, María Fernanda; Batlle Fonrodona, Francisco Javier; Costa Pinto Prego de Faria, María Joana; Perez Rodriguez, Almudena; Lourés Fraga, Esther; [et al.]
Mitral valve prosthesis leak and acquired von Willebrand syndrome (AVWS)

2011- Cuenca Castillo, Jose Joaquin; López Fernández, María Fernanda; Batlle Fonrodona, Francisco Javier; Costa Pinto Prego de Faria, María Joana; Perez Rodriguez, Almudena; [et al.]
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA

2019- Borràs N; Orriols G; Batlle Fonrodona, Francisco Javier; Perez Rodriguez, Almudena; Fidalgo T; [et al.]