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Maurizio Moggio

Showing results (1-10 of 142) with videos related to

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Current Pharmaceutical Design|January 1, 2010
Muscular dystrophies: histology, immunohistochemistry, molecular genetics and managementLamperti Costanza, Maurizio Moggio
Nutrients|June 13, 2017
Nutritional Challenges in Duchenne Muscular DystrophySimona Salera, Francesca Menni, Maurizio Moggio, et al.
Neuromuscular Disorders : NMD|May 31, 2022
A new phenotype of muscle glycogen synthase deficiency (GSD0B) characterized by an adult onset myopathy without cardiomyopathyOlimpia Musumeci, Alessia Pugliese, Rosaria Oteri, et al.
Neurology. Genetics|July 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 MutationArianna Manini, Daniele Velardo, Patrizia Ciscato, et al.
Muscle & Nerve|September 5, 2002
Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 geneGigliola Fagiolari, Monica Sciacco, Luca Chiveri, et al.
Cancer Research and Treatment|April 2, 2016
Coexistence of VHL Disease and CPT2 Deficiency: A Case ReportAlfonso Massimiliano Ferrara, Monica Sciacco, Stefania Zovato, et al.
Journal of Personalized Medicine|January 21, 2023
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular CharacterizationMichela Ripolone, Simona Zanotti, Laura Napoli, et al.
Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 25, 2015
Mitochondrial disease heterogeneity: a prognostic challengeMaurizio Moggio, Irene Colombo, Lorenzo Peverelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
Pageof 15

Showing results (1-10 of 142) with videos related to

Sort By:
Pageof 15
Current Pharmaceutical Design|January 1, 2010
Muscular dystrophies: histology, immunohistochemistry, molecular genetics and managementLamperti Costanza, Maurizio Moggio
Nutrients|June 13, 2017
Nutritional Challenges in Duchenne Muscular DystrophySimona Salera, Francesca Menni, Maurizio Moggio, et al.
Neuromuscular Disorders : NMD|May 31, 2022
A new phenotype of muscle glycogen synthase deficiency (GSD0B) characterized by an adult onset myopathy without cardiomyopathyOlimpia Musumeci, Alessia Pugliese, Rosaria Oteri, et al.
Neurology. Genetics|July 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 MutationArianna Manini, Daniele Velardo, Patrizia Ciscato, et al.
Muscle & Nerve|September 5, 2002
Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 geneGigliola Fagiolari, Monica Sciacco, Luca Chiveri, et al.
Cancer Research and Treatment|April 2, 2016
Coexistence of VHL Disease and CPT2 Deficiency: A Case ReportAlfonso Massimiliano Ferrara, Monica Sciacco, Stefania Zovato, et al.
Journal of Personalized Medicine|January 21, 2023
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular CharacterizationMichela Ripolone, Simona Zanotti, Laura Napoli, et al.
Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 25, 2015
Mitochondrial disease heterogeneity: a prognostic challengeMaurizio Moggio, Irene Colombo, Lorenzo Peverelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
Pageof 15