Showing 1 - 4 results of 4 for search 'Lochmüller Hanns', query time: 0.02s
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Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD) by Rodger Sunil, Steffensen Birgit F, Lochmüller Hanns
Published 2012-11-01Article -
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Electrophysiological features of SYT2 mutations; a novel and treatable neuromuscular syndrome by Whittaker, Roger G., Herrmann, David N., Bansagi, Boglarka, Hasan, Bashar Awwad Shiekh, Lofra, Robert Muni, Logigian, Eric L., Sowden, Janet E., Almodovar, Jorge L., Zuchner, Stephan, Horvath, Rita, Lochmüller, Hanns, Littleton, J. Troy
Published 2017
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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy by Herrmann, David N., Horvath, Rita, Sowden, Janet E., Gonzales, Michael, Sanchez-Mejias, Avencia, Whittaker, Roger G., Almodovar, Jorge L., Lane, Maria, Bansagi, Boglarka, Pyle, Angela, Boczonadi, Veronika, Lochmüller, Hanns, Griffin, Helen, Chinnery, Patrick F., Lloyd, Thomas E., Zuchner, Stephan, Guan, Zhuo, Littleton, J. Troy
Published 2017
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