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Publications by Francesco Muntoni
Biochemical and Epigenetic Modifications Occur in Muscles of Patients With Selenoprotein N Related Congenital Myopathy
Biophysical Journal
Biophysics
A Novel Morpholino Oligomer Targeting ISS-N1 Improves Rescue of Severe Spinal Muscular Atrophy Transgenic Mice
Human Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Exome Sequencing in Crisponi/CISS-like Individuals Reveals Unpredicted Alternative Diagnoses
Clinical Genetics
Genetics
Randomised Placebo-Controlled Trial of Combination ACE Inhibitor and Beta-Blocker Therapy to Prevent Cardiomyopathy in Children With Duchenne Muscular Dystrophy? (DMD Heart Protection Study): A Protocol Study
BMJ Open
Medicine
Personalized Exon Skipping Strategies to Address Clustered Non-Deletion Dystrophin Mutations
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
240th ENMC Workshop: The Involvement of Skeletal Muscle Stem Cells in the Pathology of Muscular Dystrophies 25 – 27 January 2019, Hoofddorp, the Netherlands
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
A Multicenter Comparison of Quantification Methods for Antisense Oligonucleotide-Induced DMD Exon 51 Skipping in Duchenne Muscular Dystrophy Cell Cultures
PLoS ONE
Multidisciplinary
Revised Upper Limb Module for Spinal Muscular Atrophy: 12 Month Changes
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Safety and Effectiveness of Ataluren: Comparison of Results From the STRIDE Registry and CINRG DMD Natural History Study
Journal of Comparative Effectiveness Research
Health Policy
Localization and Functional Analysis of the LARGE Family of Glycosyltransferases: Significance for Muscular Dystrophy
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
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