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Experimental Cell Research|January 7, 2014
Biomarkers in rare neuromuscular diseasesChiara Scotton, Chiara Passarelli, Marcella Neri, et al.Neuromuscular Disorders : NMD|February 24, 2005
Recurrent syncope as persistently isolated feature of transthyretin amyloidotic polyneuropathyGiuseppe Vita, Anna Mazzeo, Rita Di Leo, et al.Journal of Clinical Medicine|March 6, 2021
Innovative Therapeutic Approaches for Duchenne Muscular DystrophyFernanda Fortunato, Rachele Rossi, Maria Sofia Falzarano, et al.Molecules (Basel, Switzerland)|October 13, 2015
Duchenne Muscular Dystrophy: From Diagnosis to TherapyMaria Sofia Falzarano, Chiara Scotton, Chiara Passarelli, et al.Biochemical and Biophysical Research Communications|April 20, 2004
In vivo study of an aberrant dystrophin exon inclusion in X-linked dilated cardiomyopathyNiaz Cohen, Paola Rimessi, Francesca Gualandi, et al.Molecular Syndromology|August 25, 2018
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the LiteratureGiulia Parmeggiani, Barbara Buldrini, Sergio Fini, et al.Frontiers in Neurology|January 30, 2024
<i>DMD</i> deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosisFernanda Fortunato, Laura Tonelli, Marianna Farnè, et al.Human Mutation|January 7, 2012
Rapid, comprehensive analysis of the dystrophin transcript by a custom micro-fluidic exome arrayMatteo Bovolenta, Chiara Scotton, Maria Sofia Falzarano, et al.Journal of Cardiovascular Development and Disease|June 28, 2016
The Popeye Domain Containing Genes and their Function in Striated MuscleRoland Fr Schindler, Chiara Scotton, Vanessa French, et al.Molecules (Basel, Switzerland)|April 6, 2017
Antisense Oligonucleotide-Based Therapy for Neuromuscular DiseaseValentina Sardone, Haiyan Zhou, Francesco Muntoni, et al.Pageof 19