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Journal of the Peripheral Nervous System : JPNS|January 3, 2013
X-linked Charcot-Marie-Tooth diseaseSteven S Scherer, Kleopas A KleopaNeuromolecular Medicine|June 16, 2006
Molecular genetics of X-linked Charcot-Marie-Tooth diseaseKleopas A Kleopa, Steven S SchererJournal of Neuroscience Research|July 12, 2002
Cellular mechanisms of connexin32 mutations associated with CNS manifestationsKleopas A Kleopa, Sabrina W Yum, Steven S SchererBrain Research|July 10, 2012
How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?Kleopas A Kleopa, Charles K Abrams, Steven S SchererNeurobiology of Disease|December 4, 2002
Diverse trafficking abnormalities of connexin32 mutants causing CMTXSabrina W Yum, Kleopas A Kleopa, Susan Shumas, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 6, 2004
KCNQ2 is a nodal K+ channelJérôme J Devaux, Kleopas A Kleopa, Edward C Cooper, et al.Brain : a Journal of Neurology|April 15, 2006
Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestationsKleopas A Kleopa, Lauren B Elman, Bethan Lang, et al.Journal of Neuropathology and Experimental Neurology|August 20, 2010
Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathyNatalie Vavlitou, Irene Sargiannidou, Kyriaki Markoullis, et al.Glia|August 5, 2004
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytesKleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, et al.Pageof 24