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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.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 17, 2019
Novel <i>TRIM32</i> mutation in sarcotubular myopathyChiara Panicucci, Monica Traverso, Serena Baratto, 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.
JIMD Reports|May 1, 2017
Mutations in GMPPB Presenting with Pseudometabolic MyopathyChiara Panicucci, Chiara Fiorillo, Francesca Moro, et al.
Clinical Neuropathology|July 20, 2021
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathiesChiara Panicucci, Serena Baratto, Lizzia Raffaghello, et al.
The American Journal of Pathology|October 15, 2015
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X AxisElisabetta Gazzerro, Simona Baldassari, Stefania Assereto, et al.
European Journal of Pediatrics|November 17, 2025
Hand X-ray metrics for assessing bone health and fracture risk in Duchenne muscular dystrophy: a cross-sectional studyChiara Panicucci, Agnese Repetto, Alessia Angelelli, et al.
Neurobiology of Disease|August 2, 2025
Nusinersen corrects L-arginine deficiency in the cerebrospinal fluid of patients with severe spinal muscular atrophyAmber Hassan, Raffaella di Vito, Anna Caretto, et al.
Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Communications Medicine|February 16, 2026
Nusinersen rescues taurine deficiency in patients with type 1 Spinal Muscular AtrophyRaffaella di Vito, Amber Hassan, Tommaso Nuzzo, et al.
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