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Marina Fanin

Showing results (11-20 of 56) with videos related to

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Human Mutation|July 17, 2010
Transcriptional and translational effects of intronic CAPN3 gene mutationsAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Neuromuscular Disorders : NMD|February 24, 2005
The frequency of limb girdle muscular dystrophy 2A in northeastern ItalyMarina Fanin, Anna Chiara Nascimbeni, Luigi Fulizio, et al.
Journal of Neuromuscular Diseases|November 19, 2016
New Pathogenetic Mechanisms that Link Autophagy to Pompe DiseaseAnna Chiara Nascimbeni, Marina Fanin, Corrado Angelini, et al.
Journal of Neuropathology and Experimental Neurology|March 17, 2009
Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?Marina Fanin, Elisabetta Tasca, Anna Chiara Nascimbeni, et al.
Neurology|February 21, 2008
Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiencyAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophyCorrado Angelini, Elisabetta Tasca, Anna Chiara Nascimbeni, et al.
Human Molecular Genetics|February 26, 2014
Unveiling the degradative route of the V247M α-sarcoglycan mutant responsible for LGMD-2DElisa Bianchini, Marina Fanin, Kamel Mamchaoui, et al.
Neurology. Genetics|April 12, 2016
GYG1 gene mutations in a family with polyglucosan body myopathyMarina Fanin, Annalaura Torella, Marco Savarese, et al.
Autophagy|September 4, 2012
Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patientsAnna Chiara Nascimbeni, Marina Fanin, Eva Masiero, et al.
Neuropathology and Applied Neurobiology|January 7, 2015
Impaired autophagy affects acid α-glucosidase processing and enzyme replacement therapy efficacy in late-onset glycogen storage disease type IIAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Human Mutation|July 17, 2010
Transcriptional and translational effects of intronic CAPN3 gene mutationsAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Neuromuscular Disorders : NMD|February 24, 2005
The frequency of limb girdle muscular dystrophy 2A in northeastern ItalyMarina Fanin, Anna Chiara Nascimbeni, Luigi Fulizio, et al.
Journal of Neuromuscular Diseases|November 19, 2016
New Pathogenetic Mechanisms that Link Autophagy to Pompe DiseaseAnna Chiara Nascimbeni, Marina Fanin, Corrado Angelini, et al.
Journal of Neuropathology and Experimental Neurology|March 17, 2009
Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?Marina Fanin, Elisabetta Tasca, Anna Chiara Nascimbeni, et al.
Neurology|February 21, 2008
Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiencyAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophyCorrado Angelini, Elisabetta Tasca, Anna Chiara Nascimbeni, et al.
Human Molecular Genetics|February 26, 2014
Unveiling the degradative route of the V247M α-sarcoglycan mutant responsible for LGMD-2DElisa Bianchini, Marina Fanin, Kamel Mamchaoui, et al.
Neurology. Genetics|April 12, 2016
GYG1 gene mutations in a family with polyglucosan body myopathyMarina Fanin, Annalaura Torella, Marco Savarese, et al.
Autophagy|September 4, 2012
Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patientsAnna Chiara Nascimbeni, Marina Fanin, Eva Masiero, et al.
Neuropathology and Applied Neurobiology|January 7, 2015
Impaired autophagy affects acid α-glucosidase processing and enzyme replacement therapy efficacy in late-onset glycogen storage disease type IIAnna Chiara Nascimbeni, Marina Fanin, Elisabetta Tasca, et al.
Pageof 6