Showing results (21-30 of 104) with videos related to

Sort By:
Pageof 11
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 6, 2024
Myotonic dystrophies: an update on clinical features, molecular mechanisms, management, and gene therapyMartina Rimoldi, Sabrina Lucchiari, Serena Pagliarani, et al.
Frontiers in Neurology|October 18, 2021
First Family of <i>MATR3</i>-Related Distal Myopathy From Italy: The Role of Muscle Biopsy in the Diagnosis and Characterization of a Still Poorly Understood DiseaseMichele Cavalli, Rosanna Cardani, Laura Valentina Renna, et al.
Neuromuscular Disorders : NMD|April 7, 2009
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2Rosanna Cardani, Simona Baldassa, Annalisa Botta, et al.
European Journal of Applied Physiology|February 15, 2017
Electromechanical delays during a fatiguing exercise and recovery in patients with myotonic dystrophy type 1Fabio Esposito, Emiliano Cè, Susanna Rampichini, et al.
Frontiers in Neuroscience|February 9, 2018
MSA Mimic? Rare Occurrence of Anti-Hu Autonomic Failure and Thymoma in a Patient with Parkinsonism: Case Report and Literature ReviewVito A G Ricigliano, Barbara Fossati, Lorenzo Saraceno, et al.
Plos One|July 7, 2012
Deregulated microRNAs in myotonic dystrophy type 2Simona Greco, Alessandra Perfetti, Pasquale Fasanaro, et al.
Neuromuscular Disorders : NMD|April 1, 2014
Plasma microRNAs as biomarkers for myotonic dystrophy type 1Alessandra Perfetti, Simona Greco, Enrico Bugiardini, et al.
Neuromuscular Disorders : NMD|December 21, 2010
Dysregulation and cellular mislocalization of specific miRNAs in myotonic dystrophy type 1Riccardo Perbellini, Simona Greco, Gianluca Sarra-Ferraris, et al.
Molecular Therapy. Nucleic Acids|December 17, 2017
CRISPR/Cas9-Mediated Deletion of CTG Expansions Recovers Normal Phenotype in Myogenic Cells Derived from Myotonic Dystrophy 1 PatientsClaudia Provenzano, Marisa Cappella, Rea Valaperta, et al.
Neurobiology of Disease|February 9, 2010
Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathwaysFrancesco Rusconi, Enzo Mancinelli, Graziano Colombo, et al.
Pageof 11