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Nereo Bresolin

Showing results (251-260 of 346) with videos related to

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Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Journal of Neurology|December 17, 2013
Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesisAndrea Citterio, Alessia Arnoldi, Elena Panzeri, et al.
Journal of Neurology|February 26, 2009
Candidate gene analysis of selectin cluster in patients with multiple sclerosisChiara Fenoglio, Diego Scalabrini, Laura Piccio, et al.
Cancer Research|April 6, 2007
Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal modelsFederica Pisati, Marzia Belicchi, Francesco Acerbi, et al.
Science Translational Medicine|December 21, 2012
Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophyStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Pediatric Neurology|March 1, 2006
Agenesis of the corpus callosum: clinical and genetic study in 63 young patientsMaria Francesca Bedeschi, Maria Clara Bonaglia, Rita Grasso, et al.
Journal of the Neurological Sciences|November 11, 2021
CACNA1S mutation associated with a case of juvenile-onset congenital myopathyEleonora Mauri, Daniela Piga, Serena Pagliarani, et al.
Journal of Cellular and Molecular Medicine|July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophyDelia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 17, 2012
Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degenerationDaniela Galimberti, Claudio D'Addario, Bernardo Dell'osso, et al.
Pageof 35

Showing results (251-260 of 346) with videos related to

Sort By:
Pageof 35
Journal of the Neurological Sciences|November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunctionStefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Journal of Neurology|December 17, 2013
Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesisAndrea Citterio, Alessia Arnoldi, Elena Panzeri, et al.
Journal of Neurology|February 26, 2009
Candidate gene analysis of selectin cluster in patients with multiple sclerosisChiara Fenoglio, Diego Scalabrini, Laura Piccio, et al.
Cancer Research|April 6, 2007
Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal modelsFederica Pisati, Marzia Belicchi, Francesco Acerbi, et al.
Science Translational Medicine|December 21, 2012
Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophyStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Pediatric Neurology|March 1, 2006
Agenesis of the corpus callosum: clinical and genetic study in 63 young patientsMaria Francesca Bedeschi, Maria Clara Bonaglia, Rita Grasso, et al.
Journal of the Neurological Sciences|November 11, 2021
CACNA1S mutation associated with a case of juvenile-onset congenital myopathyEleonora Mauri, Daniela Piga, Serena Pagliarani, et al.
Journal of Cellular and Molecular Medicine|July 26, 2022
MicroRNAs as serum biomarkers in Becker muscular dystrophyDelia Gagliardi, Mafalda Rizzuti, Roberta Brusa, et al.
Parkinsonism & Related Disorders|March 10, 2019
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathyEdoardo Monfrini, Letizia Straniero, Sara Bonato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 17, 2012
Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degenerationDaniela Galimberti, Claudio D'Addario, Bernardo Dell'osso, et al.
Pageof 35