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Brain : a Journal of Neurology|August 19, 2006
CHRND mutation causes a congenital myasthenic syndrome by impairing co-clustering of the acetylcholine receptor with rapsynJuliane S Müller, Sarah K Baumeister, Ulrike Schara, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 14, 2022
Rituximab in juvenile myasthenia gravis-an international cohort study and literature reviewSithara Ramdas, Adela Della Marina, Monique M Ryan, et al.
Archives of Neurology|July 16, 2008
Aquaporin-4 antibodies in neuromyelitis optica and longitudinally extensive transverse myelitisPatrick Waters, Sven Jarius, Edward Littleton, et al.
Neuromuscular Disorders : NMD|November 30, 2020
Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporterPedro M Rodríguez Cruz, Imelda Hughes, Adnan Manzur, 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.
Journal of the Neurological Sciences|November 20, 2022
Motor end-plate analysis to diagnose immune-mediated myasthenia gravis in seronegative patientsAtsushi Nagaoka, Akira Tsujino, Hirokazu Shiraishi, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 15, 2010
Congenital myasthenic syndrome due to homozygous CHRNE mutations: report of patients in ArabiaMustafa A Salih, Darren T Oystreck, Yasser H Al-Faky, et al.
Brain : a Journal of Neurology|October 22, 2019
β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structureAn E Vanhaesebrouck, Richard Webster, Susan Maxwell, et al.
Journal of Cell Science|April 8, 2017
Multiple roles of integrin-α3 at the neuromuscular junctionJacob A Ross, Richard G Webster, Tanguy Lechertier, et al.
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