Serum Tryptase Monitoring in Indolent Systemic Mastocytosis: Association with Disease Features and Patient Outcome

por Matito, Almudena, Morgado, José Mario, Álvarez-Twose, Iván, Laura Sánchez-Muñoz, Pedreira, Carlos Eduardo, Jara-Acevedo, María, Teodosio, Cristina, Sánchez-López, Paula, Fernández-Núñez, Elisa, Moreno-Borque, Ricardo, García-Montero, Andrés, Orfao, Alberto, Escribano, Luis
Publicado 2013

Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

por Estañ, María Cristina, Fernández-Núñez, Elisa, Zaki, Maha S., Esteban, María Isabel, Donkervoort, Sandra, Hawkins, Cynthia, Caparros-Martin, José A., Saade, Dimah, Hu, Ying, Bolduc, Véronique, Chao, Katherine Ru-Yui, Nevado, Julián, Lamuedra, Ana, Largo, Raquel, Herrero-Beaumont, Gabriel, Regadera, Javier, Hernandez-Chico, Concepción, Tizzano, Eduardo F., Martinez-Glez, Victor, Carvajal, Jaime J., Zong, Ruiting, Nelson, David L., Otaify, Ghada A., Temtamy, Samia, Aglan, Mona, Issa, Mahmoud, Bönnemann, Carsten G., Lapunzina, Pablo, Yoon, Grace, Ruiz-Perez, Victor L.
Publicado 2019