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Gaetano Vattemi

Showing results (31-40 of 55) with videos related to

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Journal of Neurology|January 31, 2020
Multiple acyl-COA dehydrogenase deficiency in elderly carriersFrancesco Macchione, Leonardo Salviati, Andrea Bordugo, et al.
International Journal of Molecular Sciences|December 11, 2025
Recurrent <i>CAPN3</i> p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical ExpressivityGiorgia D'Este, Alejandro Giorgetti, Denise Cassandrini, et al.
Iscience|April 20, 2026
CryAB-driven amyloidogenesis in <i>Drosophila</i> muscle engages extracellular vesicle pathways for cellular releaseZiwei Zhao, Hui-Ying Lim, Elena Cannone, et al.
Journal of Neuropathology and Experimental Neurology|September 3, 2017
Bortezomib-Induced Muscle Toxicity in Multiple MyelomaValeria Guglielmi, Dominika Nowis, Martina Tinelli, et al.
Muscle & Nerve|August 24, 2019
Benign acute viral myositis in African migrants: A clinical, serological, and pathological studyElia Pancheri, Massimiliano Lanzafame, Alberto Zamò, et al.
Gene|March 5, 2025
A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysisMuhammad Abrar Yousaf, Arianna Scartezzini, Chiara Colombo, et al.
Journal of Neuropathology and Experimental Neurology|February 10, 2010
Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutationGaetano Vattemi, Francesca Gualandi, Arie Oosterhof, et al.
Nucleic Acids Research|July 10, 2025
Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesisValentina Salsi, Francesca Losi, Bruno Fosso, et al.
Journal of Biomedicine & Biotechnology|October 24, 2012
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx miceElena Bassi, Sofia Falzarano, Marina Fabris, et al.
Clinical Genetics|August 8, 2023
A novel in-frame deletion in MYOT causes an early adult onset distal myopathyValeria Guglielmi, Elia Pancheri, Elena Cannone, et al.
Pageof 6

Showing results (31-40 of 55) with videos related to

Sort By:
Pageof 6
Journal of Neurology|January 31, 2020
Multiple acyl-COA dehydrogenase deficiency in elderly carriersFrancesco Macchione, Leonardo Salviati, Andrea Bordugo, et al.
International Journal of Molecular Sciences|December 11, 2025
Recurrent <i>CAPN3</i> p.Asp753Asn Variant Supports a Potential Dominant Calpainopathy with Variable Clinical ExpressivityGiorgia D'Este, Alejandro Giorgetti, Denise Cassandrini, et al.
Iscience|April 20, 2026
CryAB-driven amyloidogenesis in <i>Drosophila</i> muscle engages extracellular vesicle pathways for cellular releaseZiwei Zhao, Hui-Ying Lim, Elena Cannone, et al.
Journal of Neuropathology and Experimental Neurology|September 3, 2017
Bortezomib-Induced Muscle Toxicity in Multiple MyelomaValeria Guglielmi, Dominika Nowis, Martina Tinelli, et al.
Muscle & Nerve|August 24, 2019
Benign acute viral myositis in African migrants: A clinical, serological, and pathological studyElia Pancheri, Massimiliano Lanzafame, Alberto Zamò, et al.
Gene|March 5, 2025
A novel de novo GFAP variant causes a juvenile-onset Alexander disease with bilateral vocal cord paralysisMuhammad Abrar Yousaf, Arianna Scartezzini, Chiara Colombo, et al.
Journal of Neuropathology and Experimental Neurology|February 10, 2010
Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutationGaetano Vattemi, Francesca Gualandi, Arie Oosterhof, et al.
Nucleic Acids Research|July 10, 2025
Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesisValentina Salsi, Francesca Losi, Bruno Fosso, et al.
Journal of Biomedicine & Biotechnology|October 24, 2012
Persistent dystrophin protein restoration 90 days after a course of intraperitoneally administered naked 2'OMePS AON and ZM2 NP-AON complexes in mdx miceElena Bassi, Sofia Falzarano, Marina Fabris, et al.
Clinical Genetics|August 8, 2023
A novel in-frame deletion in MYOT causes an early adult onset distal myopathyValeria Guglielmi, Elia Pancheri, Elena Cannone, et al.
Pageof 6