Steven H. Laval
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 13 publications
Autologous skeletal muscle derived cells expressing a novel functional dystrophin provide a potential therapy for Duchenne Muscular Dystrophy.
Journal: Scientific reports
Published: September 22, 2015
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome.
Journal: Brain : a journal of neurology
Published: September 01, 2015
Development and Application of an Ultrasensitive Hybridization-Based ELISA Method for the Determination of Peptide-Conjugated Phosphorodiamidate Morpholino Oligonucleotides.
Journal: Nucleic acid therapeutics
Published: July 16, 2015
Cardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic Cardiomyopathy.
Journal: Stem cells and development
Published: March 10, 2015
Absence of Cardiac Benefit with Early Combination ACE Inhibitor and Beta Blocker Treatment in mdx Mice.
Journal: Journal of cardiovascular translational research
Published: February 25, 2015
Dystrophin quantification: Biological and translational research implications.
Journal: Neurology
Published: October 31, 2014
Assessment of ventricular function in mouse models of muscular dystrophy: a comparison of MRI with conductance catheter.
Journal: Neuromuscular disorders : NMD
Published: July 31, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.
Journal: Brain : a journal of neurology
Published: June 22, 2014
Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular Transmission.
Journal: Journal of neuromuscular diseases
Published: January 01, 2014
Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy.
Journal: Human molecular genetics
Published: December 17, 2013
Exon skipping and gene transfer restore dystrophin expression in human induced pluripotent stem cells-cardiomyocytes harboring DMD mutations.
Journal: Stem cells and development
Published: July 09, 2013
Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.
Journal: Brain : a journal of neurology
Published: February 14, 2013
Last Updated: 09/26/2026