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The Japanese Dental Science Review|January 13, 2022
Biobanking in dentistry: A reviewStefano Sivolella, Anna Scanu, Zijing Xie, et al.Neuromuscular Disorders : NMD|July 22, 2020
Transportin 3 (TNPO3) and related proteins in limb girdle muscular dystrophy D2 muscle biopsies: A morphological study and pathogenetic hypothesisRoberta Costa, Maria Teresa Rodia, Sara Vianello, et al.Neurobiology of Disease|August 30, 2014
Arginine butyrate per os protects mdx mice against cardiomyopathy, kyphosis and changes in axonal excitabilitySara Vianello, Sophie Bouyon, Evelyne Benoit, et al.Human Molecular Genetics|June 9, 2017
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cellsSara Vianello, Boris Pantic, Aurora Fusto, et al.Scientific Reports|October 12, 2023
The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA)Lorenzo Blasi, Daniele Sabbatini, Andrea Fortuna, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 8, 2014
Low doses of arginine butyrate derivatives improve dystrophic phenotype and restore membrane integrity in DMD modelsSara Vianello, Francesca Consolaro, Claudia Bich, et al.Neurology. Genetics|July 30, 2025
Longitudinal Changes of Motor Function in Becker Muscular DystrophyLuca Bello, Pietro Riguzzi, Giuliana Capece, et al.European Journal of Neurology|March 17, 2026
Wernicke Encephalopathy Complicating a Distinctive POLG Phenotype With MNGIE-Like FeaturesGiuliana Capece, Luca Caumo, Sara Volta, et al.Biomolecules|November 27, 2025
<i>RYR1</i>-Related Myopathies Involve More than Calcium Dysregulation: Insights from Transcriptomic ProfilingDaniele Sabbatini, Domenico Gorgoglione, Giovanni Minervini, et al.Journal of Neurology|March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutationsPietro Riguzzi, Daniele Sabbatini, Aurora Fusto, et al.Pageof 3