Browsing by Author González Mera, Laura

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Showing results 1 to 8 of 8
Issue DateTitleAuthor(s)
14-Jun-2011Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathyOlivé i Plana, Montserrat; Odgerel, Zagaa; Martínez, Amaia; Poza, Juan José; García Bragado, Federico; Zabalza, Ramón J.; Jericó, Ivonne; González Mera, Laura; Shatunov, Alexey; Lee, Hee Suk; Armstrong i Morón, Judith; Maraví, Elías; Ramos Arroyo, María; Pascual Calvet, Jordi; Navarro, Carmen; Paradas, Carmen; Huerta Villanueva, Mariano; Márquez, Fabian; Gutierrez Rivas, Eduardo; Pou, Adolf; Ferrer, Isidro (Ferrer Abizanda); Goldfarb, Lev G.
8-Aug-2017Differences In Adipose Tissue And Lean Mass Distribution In Patients With Collagen Vi Related Myopathies Are Associated With Disease Severity And Physical AbilityRodríguez, María Angeles; Barquero, Luís M. del Rio; Ortez, Carlos Ignacio; Jou, Cristina; Vigo, Meritxell; Medina, Julita; Febrer, Anna; Ramon-Krauel, Marta; Díaz Manera, Jordi; Olivé i Plana, Montserrat; González Mera, Laura; Nascimento, Andrés; Jiménez Mallebrera, Cecilia
1-Dec-2018Muscle imaging in laminopathies: Synthesis study identifies meaningful muscles for follow-upGómez Andrés, David; Díaz Manera, Jordi; Alejaldre, Aida; Pulido Valdeolivas, Irene; González Mera, Laura; Olivé i Plana, Montserrat; Vilchez, Juan José; López de Munain, Adolfo; Paradas, Carmen; Muelas, Nuria; Sánchez Montáñez, Ángel; Alonso Jimenez, Alicia; Gómez de la Banda, Marta; Dabaj, Ivana; Bonne, Gisèle; Munell Casadesús, Francina; Carlier, Robert Y.; Quijano Roy, Susana
1-Dec-2010Nemaline myopathy type 6: clinical and myopathological featuresOlivé i Plana, Montserrat; Goldfarb, Lev G.; Lee, Hee Suk; Odgerel, Zagaa; Blokhin, Andre; González Mera, Laura; Moreno, Dolores; Laing, Nigel G.; Sambuughin, Nyamkhishig
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)
23-Oct-2012Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathyJuan Mateu, Jonàs; Rodríguez, Maria José; Nascimento, Andrés; Jiménez Mallebrera, Cecilia; González Quereda, Lidia; Rivas, Eloy; Paradas, Carmen; Madruga, Marcos; Sánchez Ayaso, Pedro; Jou, Cristina; González Mera, Laura; Munell Casadesús, Francina; Roig Quilis, Manuel; Rabasa, Maria; Hernández Lain, Aurelio; Díaz Manera, Jordi; Gallardo, Eduard; Pascual Calvet, Jordi; Verdura, Edgard; Colomer Oferil, Jaume; Baiget Bastús, Montserrat; Olivé i Plana, Montserrat; Gallano, Pia
1-May-2020Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in SpainGonzález Quereda, Lidia; Rodríguez, Maria Jose; Diaz Manera, Jordi; Alonso Pérez, Jorge; Gallardo, Eduard; Nascimento, Andrés; Ortez, Carlos Ignacio; Natera de Benito, Daniel; Olivé i Plana, Montserrat; González Mera, Laura; López de Munain, Adolfo; Zulaica, Miren; Poza, Juan Jose; Jerico, Ivonne; Tome, Laura; Riera, Pau; Milisenda, José; Sánchez, Aurora; Garrabou Tornos, Glòria; Llano, Isabel; Madruga Garrido, Marcos; Gallano, Pia
Dec-2008Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patientOlivé i Plana, Montserrat; Shatunov, Alexey; González Mera, Laura; Carmona, Olga; Moreno, Dolores; González Quereda, Lidia; Martínez Matos, Juan Antonio; Goldfarb, Lev G.; Ferrer, Isidro (Ferrer Abizanda)