Browsing by Author Miralles, Francesc

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Issue DateTitleAuthor(s)
6-Jan-2019Late-onset thymidine kinase 2 deficiency: a review of 18 casesDomínguez González, Cristina; Hernández lain, Aurelio; Rivas, Eloy; Hernández Voth, Ana; Sayas Catalán, Javier; Fernández Torrón, Roberto; Fuiza Luces, Carmen; García García, Jorge; Morís, Germán; Olivé i Plana, Montserrat; Miralles, Francesc; Díaz Manera, Jordi; Caballero, Candela; Méndez Ferrer, Bosco; Martí, Ramon; García Arumí, Elena; Badosa, Carmen; Esteban, Jesús; Jiménez-Mallebrera, Cecilia; Blázquez Encinar, Alberto; Arenas, Joaquín; Hirano, Michio; Martin, Miguel Ángel; Paradas, Carmen
1-Jan-2019Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsOlivé i Plana, Montserrat; Engvall, Martin; Ravenscroft, Gianina; Cabrera Serrano, Macarena; Jiao, Hong; Bortolotti, Carlo Augusto; Pignataro, Marcello; Lambrughi, Matteo; Jiang, Haibo; Forrest, Alistair R. R.; Benseny Cases, Núria; Hofbauer, Stefan; Obinger, Christian; Battistuzzi, Gianantonio; Bellei, Marzia; Borsari, Marco; Di Rocco, Giulia; Viola, Helena M.; Hoo, Livia C.; Cladera, Josep; Lagerstedt Robinson, Kristina; Xiang, Fengqing; Wredenberg, Anna; Miralles, Francesc; Baiges, Juan José; Malfatti, Edoardo; Romero, Norma B.; Streichenberger, Nathalie; Via, Christophe; Claeys, Kristl G.; Straathof, Chiara S.M; Goris, An; Freyer, Christoph; Lammens, Martin; Bassez, Guillaume; Kere, Juha; Clemente, Paula; Sejersen, Thomas; Udd, Bjarne; Vidal, Noemí; Ferrer, Isidro (Ferrer Abizanda); Edstrom, Lars; Wedell, Anna; Laing, Nigel G.
Jun-2007Phenotypic patterns of desminopathy associated with three novel mutations in the desmin geneOlivé i Plana, Montserrat; Armstrong i Morón, Judith; Miralles, Francesc; Pou, Adolf; Fardeau, Michel; González Mera, Laura; Martínez, Francesca; Fisher, Dirk; Martínez Matos, Juan Antonio; Shatunov, Alexey; Goldfarb, Lev G.; Ferrer, Isidro (Ferrer Abizanda)