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P Camaño

Showing results (1-10 of 6) with videos related to

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Genes, Brain, and Behavior|October 1, 2008
Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defectA Sistiaga, P Camaño, D Otaegui, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 12, 2006
CD24 V/V is an allele associated with the risk of developing multiple sclerosis in the Spanish populationD Otaegui, A Sáenz, P Camaño, et al.
Neurology|October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMAM Mancuso, L Salviati, S Sacconi, et al.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genes, Brain, and Behavior|October 1, 2008
Cognitive function in facioscapulohumeral dystrophy correlates with the molecular defectA Sistiaga, P Camaño, D Otaegui, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 12, 2006
CD24 V/V is an allele associated with the risk of developing multiple sclerosis in the Spanish populationD Otaegui, A Sáenz, P Camaño, et al.
Neurology|October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMAM Mancuso, L Salviati, S Sacconi, et al.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Pageof 1