AAAAAA
Results:
1-16
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Results: 16
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:
Toepfer, M
Schroeder, M
Muller-Felber, W
Lochmuller, H
Sitter, T
Pongratz, D
Schiffl, H
Citation: M. Toepfer et al., Successful management of polyneuropathy associated with IgM gammopathy of undetermined significance with antibody-based immunoadsorption, CLIN NEPHR, 53(5), 2000, pp. 404-407
Authors:
Klopstock, T
Querner, V
Schmidt, F
Gekeler, F
Walter, M
Hartard, M
Hennig, M
Gasser, T
Pongratz, D
Straube, A
Dieterich, M
Muller-Felber, W
Citation: T. Klopstock et al., A placebo-controlled crossover trial of creatine in mitochondrial diseases, NEUROLOGY, 55(11), 2000, pp. 1748-1751
Authors:
Walter, MC
Lochmuller, H
Reilich, P
Klopstock, T
Huber, R
Hartard, M
Hennig, M
Pongratz, D
Muller-Felber, W
Citation: Mc. Walter et al., Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study, NEUROLOGY, 54(9), 2000, pp. 1848-1850
Authors:
Muller-Felber, W
Citation: W. Muller-felber, Neurological aspects of peripheral neuropathy in diabetes, INTERNIST, 41(5), 2000, pp. 429-433
Authors:
Landgraf, R
Muller-Felber, W
Piehlmeier, W
Dieterle, C
Citation: R. Landgraf et al., Impact of pancreas/islet transplantation on the course of diabetic complications, DIABETES IN THE NEW MILLENNIUM, 2000, pp. 355-366
Authors:
Toepfer, M
Folwaczny, C
Klauser, A
Riepl, RL
Muller-Felber, W
Pongratz, D
Citation: M. Toepfer et al., Gastrointestinal dysfunction in amyotrophic lateral sclerosis, AMYOTROPH L, 1(1), 1999, pp. 15-19
Authors:
Muller-Felber, W
Ansevin, CF
Ricker, K
Muller-Jenssen, A
Topfer, M
Goebel, HH
Pongratz, DE
Citation: W. Muller-felber et al., Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis, NEUROMUSC D, 9(8), 1999, pp. 604-607
Authors:
Muller-Felber, W
Schlotter, B
Topfer, M
Ketelsen, UP
Muller-Hocker, J
Pongratz, D
Citation: W. Muller-felber et al., Phenotypic variability in two brothers with sarcotubular myopathy, J NEUROL, 246(5), 1999, pp. 408-411
Authors:
Toepfer, M
Schroeder, M
Unger, JW
Lochmuller, H
Pongratz, D
Muller-Felber, W
Citation: M. Toepfer et al., Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies), CLIN NEUROL, 101(3), 1999, pp. 207-209
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:
Schulze, J
Toepfer, M
Schroff, KC
Aschhoff, S
Remien, J
Muller-Felber, W
Endres, S
Citation: J. Schulze et al., Clindamycin and nicotinic neuromuscular transmission, LANCET, 354(9192), 1999, pp. 1792-1793
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:
Toepfer, M
Folwaczny, C
Lochmuller, H
Schroeder, M
Riepl, RL
Pongratz, D
Muller-Felber, W
Citation: M. Toepfer et al., Noninvasive C-13-octanoic acid breath test shows delayed gastric emptying in patients with amyotrophic lateral sclerosis, DIGESTION, 60(6), 1999, pp. 567-571
Authors:
Klopstock, T
Chahrokh-Zadeh, S
Holinski-Feder, E
Meindl, A
Gasser, T
Pongratz, D
Muller-Felber, W
Citation: T. Klopstock et al., Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene, ACT NEUROP, 97(2), 1999, pp. 139-142
Risultati:
1-16
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