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Human Molecular Genetics|May 5, 2017
Oxidative stress in Duchenne muscular dystrophy: focus on the NRF2 redox pathwaySara Petrillo, Laura Pelosi, Fiorella Piemonte, et al.
International Journal of Cardiology|January 29, 2019
Heart rate reduction strategy using ivabradine in end-stage Duchenne cardiomyopathyRachele Adorisio, Camilla Calvieri, Nicoletta Cantarutti, et al.
Neuromuscular Disorders : NMD|December 4, 2019
Evaluation of gait in Duchenne Muscular Dystrophy: Relation of 3D gait analysis to clinical assessmentAlberto Romano, Martina Favetta, Tommaso Schirinzi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 6, 2021
Management of motor rehabilitation in individuals with muscular dystrophies. 1st Consensus Conference report from UILDM - Italian Muscular Dystrophy Association (Rome, January 25-26, 2019)Maria Elena Lombardo, Elena Carraro, Cristina Sancricca, et al.
Journal of Neurology|January 7, 2015
"Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutationMichela Catteruccia, Donato Sauchelli, Giacomo Della Marca, et al.
Muscle & Nerve|August 9, 2021
Age-related sensory neuropathy in patients with spinal muscular atrophy type 1Stefano Pro, Alberto Eugenio Tozzi, Adele D'Amico, et al.
Frontiers in Cellular Neuroscience|August 8, 2024
Modeling riboflavin transporter deficiency type 2: from iPSC-derived motoneurons to iPSC-derived astrocytesValentina Magliocca, Angela Lanciotti, Elena Ambrosini, et al.
Neuromuscular Disorders : NMD|February 10, 2024
Evolution of neuropsychological and behavioral profile in a cohort of pediatric patients with Becker muscular dystrophy in a longitudinal studyFrancesca Cumbo, Michele Tosi, Michela Catteruccia, et al.
Molecular Genetics and Metabolism|February 4, 2014
Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patientsMichela Catteruccia, Daniela Verrigni, Diego Martinelli, et al.
Journal of Medical Genetics|December 18, 2012
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutationsMarianna Ciccolella, Stefania Corti, Michela Catteruccia, et al.
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