Authors: Jahn, K Mohammadi, B Krampfl, K Abicht, A Lochmuller, H Bufler, J

Citation: K. Jahn et al., Deactivation and desensitization of mouse embryonic- and adult-type nicotinic receptor channel currents, NEUROSCI L, 307(2), 2001, pp. 89-92

Authors: Stucka, R Abicht, A Song, IH Bonsch, D Deufel, T Lochmuller, H

Citation: R. Stucka et al., A modified alignment of human and rodent 5 ' untranslated sequences of theacetylcholine receptor epsilon subunit gene reveals additional regions of high homology, NEUROMUSC D, 10(3), 2000, pp. 213-214

Authors: Horvath, R Abicht, A Shoubridge, EA Karcagi, V Rozsa, C Komoly, S Lochmuller, H

Citation: R. Horvath et al., Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS, J NEUROL, 247(1), 2000, pp. 65-67

Authors: Toepfer, M Fischer, P Abicht, A Lochmuller, H Pongratz, D Muller-Felber, W

Citation: M. Toepfer et al., Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle, CELL MOL N, 19(2), 1999, pp. 297-300

Authors: Abicht, A Stucka, R Karcagi, V Herczegfalvi, A Horvath, R Mortier, W Schara, U Ramaekers, V Jost, W Brunner, J Janssen, G Seidel, U Schlotter, B Muller-Felber, W Pongratz, D Rudel, R Lochmuller, H

Citation: A. Abicht et al., A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin, NEUROLOGY, 53(7), 1999, pp. 1564-1569

Authors: Kramer, R Lochmuller, H Abicht, A Rudel, R Brinkmeier, H

Citation: R. Kramer et al., Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice, NEUROMUSC D, 8(8), 1998, pp. 542-550