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Filippo M Santorelli

Showing results (1-10 of 294) with videos related to

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Cerebellum (London, England)|July 5, 2022
Correction to: The Strange Case of the Multiple MRI Phenotypes of RFC1 MutationMario Mascalchi, Filippo M Santorelli
Molecular Genetics and Metabolism Reports|June 23, 2016
Reply to: Double trouble progressive external ophthalmoplegia and Huntington's diseaseMassimiliano Filosto, Filippo M Santorelli
Cerebellum (London, England)|April 1, 2022
The Strange Case of the Multiple MRI Phenotypes of RFC1 MutationMario Mascalchi, Filippo M Santorelli
Genes|April 28, 2023
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special IssueLuisa Politano, Filippo M Santorelli
Archives of Neurology|December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencingGabriella Silvestri, Marcella Masciullo, Filippo M Santorelli
Hepatology Research : the Official Journal of the Japan Society of Hepatology|October 26, 2012
Reply from the authorsIsabella Giovannoni, Paola Francalanci, Filippo M Santorelli
Handbook of Clinical Neurology|April 30, 2013
Hereditary spastic paraplegias: one disease for many genes, and still countingPaola S Denora, Filippo M Santorelli, Enrico Bertini
Movement Disorders Clinical Practice|August 11, 2020
<i>STUB1</i>-Related Ataxias: A Challenging DiagnosisSirio Cocozza, Filippo M Santorelli, Giuseppe De Michele
Neurogenetics|December 7, 2017
Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysisDaniele Galatolo, Alessandra Tessa, Alessandro Filla, et al.
Electrophoresis|October 27, 2007
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell linesIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Pageof 30

Showing results (1-10 of 294) with videos related to

Sort By:
Pageof 30
Cerebellum (London, England)|July 5, 2022
Correction to: The Strange Case of the Multiple MRI Phenotypes of RFC1 MutationMario Mascalchi, Filippo M Santorelli
Molecular Genetics and Metabolism Reports|June 23, 2016
Reply to: Double trouble progressive external ophthalmoplegia and Huntington's diseaseMassimiliano Filosto, Filippo M Santorelli
Cerebellum (London, England)|April 1, 2022
The Strange Case of the Multiple MRI Phenotypes of RFC1 MutationMario Mascalchi, Filippo M Santorelli
Genes|April 28, 2023
Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special IssueLuisa Politano, Filippo M Santorelli
Archives of Neurology|December 12, 2012
Autosomal recessive spastic ataxia of Charlevoix-Saguenay in the time of next-generation sequencingGabriella Silvestri, Marcella Masciullo, Filippo M Santorelli
Hepatology Research : the Official Journal of the Japan Society of Hepatology|October 26, 2012
Reply from the authorsIsabella Giovannoni, Paola Francalanci, Filippo M Santorelli
Handbook of Clinical Neurology|April 30, 2013
Hereditary spastic paraplegias: one disease for many genes, and still countingPaola S Denora, Filippo M Santorelli, Enrico Bertini
Movement Disorders Clinical Practice|August 11, 2020
<i>STUB1</i>-Related Ataxias: A Challenging DiagnosisSirio Cocozza, Filippo M Santorelli, Giuseppe De Michele
Neurogenetics|December 7, 2017
Clinical application of next generation sequencing in hereditary spinocerebellar ataxia: increasing the diagnostic yield and broadening the ataxia-spasticity spectrum. A retrospective analysisDaniele Galatolo, Alessandra Tessa, Alessandro Filla, et al.
Electrophoresis|October 27, 2007
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell linesIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Pageof 30