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B Romero

Showing results (221-230 of 337) with videos related to

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Pediatric Transplantation|March 19, 1999
Bioavailability of two oral formulations of cyclosporin A in uremic children before renal transplantationM Medeiros, A C Gómez, J P Urizar, et al.
Archives of Biochemistry and Biophysics|June 28, 2024
Hexyltrimethylammonium ion enhances potential copper-chelating properties of ammonium thiomolybdate in an in vivo zebrafish modelK Vega-Granados, P Escobar-Ibarra, K Palomino-Vizcaino, et al.
Veterinary Microbiology|February 2, 2010
Experimental infection of Eurasian wild boar with Mycobacterium avium subsp. aviumJ M Garrido, J Vicente, R Carrasco-García, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related DiseasesIsabelle Nelson, Tanya Stojkovic, Valérie Allamand, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Transboundary and Emerging Diseases|February 4, 2015
Sheep as a Potential Source of Bovine TB: Epidemiology, Pathology and Evaluation of Diagnostic TechniquesM Muñoz-Mendoza, B Romero, A Del Cerro, et al.
Annals of Neurology|October 13, 2007
Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onsetMarc Bitoun, Jorge A Bevilacqua, Bernard Prudhon, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Journal of Neuromuscular Diseases|November 14, 2022
LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMDTanya Stojkovic, Marion Masingue, Corinne Métay, et al.
European Journal of Medical Genetics|January 14, 2009
POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.
Pageof 34

Showing results (221-230 of 337) with videos related to

Sort By:
Pageof 34
Pediatric Transplantation|March 19, 1999
Bioavailability of two oral formulations of cyclosporin A in uremic children before renal transplantationM Medeiros, A C Gómez, J P Urizar, et al.
Archives of Biochemistry and Biophysics|June 28, 2024
Hexyltrimethylammonium ion enhances potential copper-chelating properties of ammonium thiomolybdate in an in vivo zebrafish modelK Vega-Granados, P Escobar-Ibarra, K Palomino-Vizcaino, et al.
Veterinary Microbiology|February 2, 2010
Experimental infection of Eurasian wild boar with Mycobacterium avium subsp. aviumJ M Garrido, J Vicente, R Carrasco-García, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related DiseasesIsabelle Nelson, Tanya Stojkovic, Valérie Allamand, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Transboundary and Emerging Diseases|February 4, 2015
Sheep as a Potential Source of Bovine TB: Epidemiology, Pathology and Evaluation of Diagnostic TechniquesM Muñoz-Mendoza, B Romero, A Del Cerro, et al.
Annals of Neurology|October 13, 2007
Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onsetMarc Bitoun, Jorge A Bevilacqua, Bernard Prudhon, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Journal of Neuromuscular Diseases|November 14, 2022
LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMDTanya Stojkovic, Marion Masingue, Corinne Métay, et al.
European Journal of Medical Genetics|January 14, 2009
POMT2 intragenic deletions and splicing abnormalities causing congenital muscular dystrophy with mental retardationAkiko Yanagisawa, Céline Bouchet, Susana Quijano-Roy, et al.
Pageof 34