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Annals of Neurology|March 3, 2004
Focal caspase activation underlies the endplate myopathy in slow-channel syndromeBhupinder P S Vohra, Jason S Groshong, Ricardo A Maselli, et al.Journal of Virology|April 11, 2008
A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelinationGleb Baida, Brian Popko, Robert L Wollmann, et al.Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.Human Molecular Genetics|April 8, 2010
Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interactionRicardo A Maselli, Juan Arredondo, Orla Cagney, et al.Archives of Neurology|December 14, 2011
Acute severe animal model of anti-muscle-specific kinase myasthenia: combined postsynaptic and presynaptic changesDavid P Richman, Kayoko Nishi, Stuart W Morell, et al.The Journal of Clinical Investigation|September 15, 2007
Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndromeJason S Groshong, Melissa J Spencer, Bula J Bhattacharyya, et al.Human Genetics|December 30, 2011
LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrinRicardo A Maselli, Jose M Fernandez, Juan Arredondo, et al.Nature Genetics|December 29, 2005
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic miceSandra L Gilbert, Li Zhang, Michele L Forster, et al.Pageof 2