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Brain Pathology (Zurich, Switzerland)|December 17, 2008
A 59 year-old man with sellar lesionRobert M Sargis, Robert L Wollmann, Peter PytelAnnals of the New York Academy of Sciences|January 3, 2013
Synaptic basal lamina-associated congenital myasthenic syndromesRicardo A Maselli, Juan Arredondo, Michael J Ferns, et al.Muscle & Nerve|January 28, 2003
Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesisRicardo A Maselli, Darlene Chen, Delores Mo, et al.American Journal of Clinical Pathology|January 6, 2006
Degenerative spine disease : pathologic findings in 985 surgical specimensPeter Pytel, Robert L Wollmann, Richard G Fessler, et al.Neurobiology of Disease|July 4, 2006
Activation of apoptotic pathways at muscle fiber synapses is circumscribed and reversible in a slow-channel syndrome modelBhupinder P S Vohra, Jason S Groshong, Roberto Zayas, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 7, 2008
Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNSMaria Traka, Robert L Wollmann, Sonia R Cerda, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 28, 2007
Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 geneXiang-Jun Chen, Eleni N Levedakou, Kathleen J Millen, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 2, 2002
Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndromeChristopher M Gomez, Ricardo A Maselli, Jason Groshong, et al.Muscle & Nerve|August 21, 2003
Rapsyn mutations in myasthenic syndrome due to impaired receptor clusteringRicardo A Maselli, Vanessa Dunne, Samuel Ignacio Pascual-Pascual, et al.Muscle & Nerve|December 28, 2007
Variable phenotypes associated with mutations in DOK7Jennifer A Anderson, Jarae J Ng, Constance Bowe, et al.Pageof 2