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C Nascimbeni

Showing results (1-10 of 24) with videos related to

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Clinical Genetics|May 2, 2007
Late-onset GSDII with novel GAA gene mutationC Angelini, A C Nascimbeni
Neuropathology and Applied Neurobiology|February 19, 2013
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular studyM Fanin, A C Nascimbeni, C Angelini
Muscle & Nerve|January 8, 2014
Muscle atrophy, ubiquitin-proteasome, and autophagic pathways in dysferlinopathyMarina Fanin, Anna C Nascimbeni, Corrado Angelini
JIMD Reports|February 26, 2015
Autophagy in Natural History and After ERT in Glycogenosis Type IICorrado Angelini, Anna C Nascimbeni, Marina Fanin
Clinical Neuropathology|March 13, 2014
Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patientsMarina Fanin, Anna C Nascimbeni, Corrado Angelini
Journal of Medical Genetics|September 15, 2006
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutationsM Fanin, A C Nascimbeni, C Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 20, 2004
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutationC Angelini, G Cenacchi, A C Nascimbeni, et al.
International Review of Cell and Molecular Biology|January 11, 2017
Molecular Mechanisms of Noncanonical AutophagyN Dupont, A C Nascimbeni, E Morel, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Clinical Genetics|May 2, 2007
Late-onset GSDII with novel GAA gene mutationC Angelini, A C Nascimbeni
Neuropathology and Applied Neurobiology|February 19, 2013
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular studyM Fanin, A C Nascimbeni, C Angelini
Muscle & Nerve|January 8, 2014
Muscle atrophy, ubiquitin-proteasome, and autophagic pathways in dysferlinopathyMarina Fanin, Anna C Nascimbeni, Corrado Angelini
JIMD Reports|February 26, 2015
Autophagy in Natural History and After ERT in Glycogenosis Type IICorrado Angelini, Anna C Nascimbeni, Marina Fanin
Clinical Neuropathology|March 13, 2014
Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patientsMarina Fanin, Anna C Nascimbeni, Corrado Angelini
Journal of Medical Genetics|September 15, 2006
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutationsM Fanin, A C Nascimbeni, C Angelini
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 20, 2004
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutationC Angelini, G Cenacchi, A C Nascimbeni, et al.
International Review of Cell and Molecular Biology|January 11, 2017
Molecular Mechanisms of Noncanonical AutophagyN Dupont, A C Nascimbeni, E Morel, et al.
Clinical Genetics|March 4, 2008
Cardioembolic stroke in Danon diseaseM Spinazzi, M Fanin, P Melacini, et al.
Cell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.
Pageof 3