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Frédéric Chevessier

Max Planck Society

9

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240

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Advances in the understanding of skeletal muscle weakness in murine models of diseases affecting nerve-evoked muscle activity, motor neurons, synapses and myofibers

2014 Neuromuscular Disorders
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The neuromuscular junction: selective remodeling of synaptic regulators at the nerve/muscle interface.

2013 Mechanisms of Development
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A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation

2012 Neurobiology of Disease
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Brody syndrome represents a differential diagnosis for painless exercise -induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene

2011
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Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

2009 American Journal of Human Genetics
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Analysis of the neuromuscular junction, synaptic transmission, and muscle contraction in a knock-in mouse with a slow channel congenital myasthenic syndrome

2009
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A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions

2008 Human Molecular Genetics
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Congenital myasthenic syndrome due to mutations in the MUSK gene: Characterization of a factor favouring axonal growth

2008
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