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Claudio Bruno

Showing results (81-90 of 302) with videos related to

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Neuromuscular Disorders : NMD|October 23, 2013
Novel mutations in the fukutin gene in a boy with asymptomatic hyperCKemiaChiara Fiorillo, Francesca Moro, Guja Astrea, et al.
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.
Journal of Cellular and Molecular Medicine|May 7, 2025
D- and L-Amino Acid Blood Concentrations Are Affected in Children With Duchenne Muscular DystrophyMartina Garofalo, Chiara Panicucci, Alberto Imarisio, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|July 31, 2024
Investigating whether H5N1 is a risk to human populations in BrazilClaudio Bruno Silva de Oliveira, Joelma Maria de Araújo Andrade, Shahina Akter, et al.
Cancers|April 12, 2022
Targeting of Ubiquitin E3 Ligase RNF5 as a Novel Therapeutic Strategy in Neuroectodermal TumorsElisa Principi, Elvira Sondo, Giovanna Bianchi, et al.
Molecular Cell|April 1, 2004
Respiratory complex III is required to maintain complex I in mammalian mitochondriaRebeca Acín-Pérez, María Pilar Bayona-Bafaluy, Patricio Fernández-Silva, et al.
Neuromuscular Disorders : NMD|November 15, 2017
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experienceSonia Messina, Marika Pane, Valeria Sansone, et al.
Research in Developmental Disabilities|August 11, 2015
Reading impairment in Duchenne muscular dystrophy: A pilot study to investigate similarities and differences with developmental dyslexiaGuja Astrea, Chiara Pecini, Filippo Gasperini, et al.
Journal of Telemedicine and Telecare|June 6, 2018
Tele-monitoring in paediatric and young home-ventilated neuromuscular patients: A multicentre case-control trialFederica Trucco, Marina Pedemonte, Fabrizio Racca, et al.
Italian Journal of Pediatrics|October 17, 2022
Long term follow-up in two siblings with Sengers syndrome: Case reportChiara Panicucci, Maria Cristina Schiaffino, Claudia Nesti, et al.
Pageof 31

Showing results (81-90 of 302) with videos related to

Sort By:
Pageof 31
Neuromuscular Disorders : NMD|October 23, 2013
Novel mutations in the fukutin gene in a boy with asymptomatic hyperCKemiaChiara Fiorillo, Francesca Moro, Guja Astrea, et al.
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.
Journal of Cellular and Molecular Medicine|May 7, 2025
D- and L-Amino Acid Blood Concentrations Are Affected in Children With Duchenne Muscular DystrophyMartina Garofalo, Chiara Panicucci, Alberto Imarisio, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|July 31, 2024
Investigating whether H5N1 is a risk to human populations in BrazilClaudio Bruno Silva de Oliveira, Joelma Maria de Araújo Andrade, Shahina Akter, et al.
Cancers|April 12, 2022
Targeting of Ubiquitin E3 Ligase RNF5 as a Novel Therapeutic Strategy in Neuroectodermal TumorsElisa Principi, Elvira Sondo, Giovanna Bianchi, et al.
Molecular Cell|April 1, 2004
Respiratory complex III is required to maintain complex I in mammalian mitochondriaRebeca Acín-Pérez, María Pilar Bayona-Bafaluy, Patricio Fernández-Silva, et al.
Neuromuscular Disorders : NMD|November 15, 2017
Expanded access program with Nusinersen in SMA type I in Italy: Strengths and pitfalls of a successful experienceSonia Messina, Marika Pane, Valeria Sansone, et al.
Research in Developmental Disabilities|August 11, 2015
Reading impairment in Duchenne muscular dystrophy: A pilot study to investigate similarities and differences with developmental dyslexiaGuja Astrea, Chiara Pecini, Filippo Gasperini, et al.
Journal of Telemedicine and Telecare|June 6, 2018
Tele-monitoring in paediatric and young home-ventilated neuromuscular patients: A multicentre case-control trialFederica Trucco, Marina Pedemonte, Fabrizio Racca, et al.
Italian Journal of Pediatrics|October 17, 2022
Long term follow-up in two siblings with Sengers syndrome: Case reportChiara Panicucci, Maria Cristina Schiaffino, Claudia Nesti, et al.
Pageof 31