Authors:
Walter, MC
Lochmuller, H
Schlotter, B
Reilich, P
Muller-Felber, W
Pongratz, D
Citation: Mc. Walter et al., New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM), NERVENARZT, 72(2), 2001, pp. 117-121
Authors:
Walter, MC
Lochmuller, H
Toepfer, M
Schlotter, B
Reilich, P
Schroder, M
Muller-Felber, W
Pongratz, D
Citation: Mc. Walter et al., High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study, J NEUROL, 247(1), 2000, pp. 22-28
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:
Schlamp, V
Karg, O
Abel, A
Schlotter, B
Wasner, M
Borasio, GD
Citation: V. Schlamp et al., Non-invasive intermittent home mechanical ventilation as a palliative treatment in amyotrophic lateral sclerosis, NERVENARZT, 69(12), 1998, pp. 1074-1082