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Journal of Neurology
|
January 11, 2012
Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy
Mireia Tondo, Josep Gámez, Eduardo Gutiérrez-Rivas, et al.
Journal of Neuropathology and Experimental Neurology
|
February 20, 2009
TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies
Montse Olivé, Anna Janué, Dolores Moreno, et al.
Molecular Neurobiology
|
March 2, 2018
K<sub>ATP</sub> Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis
José M Vidal-Taboada, Marco Pugliese, Maria Salvadó, et al.
Muscle & Nerve
|
August 21, 2003
Two novel mutations in the muscle glycogen phosphorylase gene in McArdle's disease
Josep Gámez, Juan C Rubio, Miguel A Martín, et al.
Archives of Neurology
|
December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle disease
Juan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
Molecular Genetics and Metabolism
|
April 11, 2006
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA
Jordi P Guallar, Maya R Vilà, Ester López-Gallardo, et al.
Annals of Clinical and Translational Neurology
|
October 24, 2018
Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum
Mikel Vicente-Pascual, Marcello Rossi, Josep Gámez, et al.
Brain : a Journal of Neurology
|
April 2, 2013
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
Maria J Melià, Akatsuki Kubota, Saida Ortolano, et al.
Journal of Neurology
|
July 5, 2011
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia
Elena Sánchez-Ferrero, Eliecer Coto, Ana I Corao, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
September 6, 2016
A coordinated transition model for patients with cystinosis: from pediatrics to adult care
Gema Ariceta, Juan Antonio Camacho, Matilde Fernández-Obispo, et al.
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of 2
Search research articles
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Journal of Neurology
|
January 11, 2012
Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy
Mireia Tondo, Josep Gámez, Eduardo Gutiérrez-Rivas, et al.
Journal of Neuropathology and Experimental Neurology
|
February 20, 2009
TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies
Montse Olivé, Anna Janué, Dolores Moreno, et al.
Molecular Neurobiology
|
March 2, 2018
K<sub>ATP</sub> Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis
José M Vidal-Taboada, Marco Pugliese, Maria Salvadó, et al.
Muscle & Nerve
|
August 21, 2003
Two novel mutations in the muscle glycogen phosphorylase gene in McArdle's disease
Josep Gámez, Juan C Rubio, Miguel A Martín, et al.
Archives of Neurology
|
December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle disease
Juan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
Molecular Genetics and Metabolism
|
April 11, 2006
Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA
Jordi P Guallar, Maya R Vilà, Ester López-Gallardo, et al.
Annals of Clinical and Translational Neurology
|
October 24, 2018
Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum
Mikel Vicente-Pascual, Marcello Rossi, Josep Gámez, et al.
Brain : a Journal of Neurology
|
April 2, 2013
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
Maria J Melià, Akatsuki Kubota, Saida Ortolano, et al.
Journal of Neurology
|
July 5, 2011
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia
Elena Sánchez-Ferrero, Eliecer Coto, Ana I Corao, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
September 6, 2016
A coordinated transition model for patients with cystinosis: from pediatrics to adult care
Gema Ariceta, Juan Antonio Camacho, Matilde Fernández-Obispo, et al.
Page
of 2