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Carlo Minetti

Showing results (71-80 of 190) with videos related to

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Neurogenetics|July 4, 2019
Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findingsMarcello Scala, Giorgia Brigati, Chiara Fiorillo, et al.
Cannabis and Cannabinoid Research|May 17, 2021
An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant EpilepsyFrancesca Marchese, Maria Stella Vari, Ganna Balagura, et al.
Frontiers in Neurology|December 24, 2021
New Trends and Most Promising Therapeutic Strategies for Epilepsy TreatmentAntonella Riva, Alice Golda, Ganna Balagura, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutationsMafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Journal of Child Neurology|April 13, 2011
Quality of life in Duchenne muscular dystrophy: the subjective impact on children and parentsIlaria Baiardini, Carlo Minetti, Simona Bonifacino, et al.
DNA and Cell Biology|November 3, 2018
Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 GeneChiara Fiorillo, Maria Rosaria D'Apice, Federica Trucco, et al.
Italian Journal of Pediatrics|October 13, 2021
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variantsMarcello Scala, Midas Anijs, Roberta Battini, et al.
Cell Cycle (Georgetown, Tex.)|November 19, 2005
Loss of caveolin-1 causes the hyper-proliferation of intestinal crypt stem cells, with increased sensitivity to whole body gamma-radiationJiangwei Li, Ghada S Hassan, Terence M Williams, et al.
The American Journal of Pathology|September 26, 2003
Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteinsGloria Bonuccelli, Federica Sotgia, William Schubert, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2018
Spinal motor neuron involvement in a patient with homozygous PRUNE mutationMichele Iacomino, Chiara Fiorillo, Annalaura Torella, et al.
Pageof 19

Showing results (71-80 of 190) with videos related to

Sort By:
Pageof 19
Neurogenetics|July 4, 2019
Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findingsMarcello Scala, Giorgia Brigati, Chiara Fiorillo, et al.
Cannabis and Cannabinoid Research|May 17, 2021
An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant EpilepsyFrancesca Marchese, Maria Stella Vari, Ganna Balagura, et al.
Frontiers in Neurology|December 24, 2021
New Trends and Most Promising Therapeutic Strategies for Epilepsy TreatmentAntonella Riva, Alice Golda, Ganna Balagura, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutationsMafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Journal of Child Neurology|April 13, 2011
Quality of life in Duchenne muscular dystrophy: the subjective impact on children and parentsIlaria Baiardini, Carlo Minetti, Simona Bonifacino, et al.
DNA and Cell Biology|November 3, 2018
Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 GeneChiara Fiorillo, Maria Rosaria D'Apice, Federica Trucco, et al.
Italian Journal of Pediatrics|October 13, 2021
Hyperkinetic stereotyped movements in a boy with biallelic CNTNAP2 variantsMarcello Scala, Midas Anijs, Roberta Battini, et al.
Cell Cycle (Georgetown, Tex.)|November 19, 2005
Loss of caveolin-1 causes the hyper-proliferation of intestinal crypt stem cells, with increased sensitivity to whole body gamma-radiationJiangwei Li, Ghada S Hassan, Terence M Williams, et al.
The American Journal of Pathology|September 26, 2003
Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteinsGloria Bonuccelli, Federica Sotgia, William Schubert, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 9, 2018
Spinal motor neuron involvement in a patient with homozygous PRUNE mutationMichele Iacomino, Chiara Fiorillo, Annalaura Torella, et al.
Pageof 19