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Results:
1-7
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Results: 7
Authors:
Walter, MC
Lochmuller, H
Citation: Mc. Walter et H. Lochmuller, Novel approaches to treat muscular dystrophies, EXPERT OP I, 10(4), 2001, pp. 695-707
Authors:
Lampe, J
Gossrau, G
Reichmann, H
Koch, R
Walter, MC
Mendel, B
Lochmuller, H
Citation: J. Lampe et al., Prion codon 129 homozygosity and sporadic inclusion body myositis, NEUROLOGY, 57(2), 2001, pp. 368-368
Authors:
Lampe, J
Gossrau, G
Reichmann, H
Walter, MC
Mendel, B
Lochmuller, H
Citation: J. Lampe et al., Prion codon 129 homozygosity and sporadic inclusion body myositis, NEUROLOGY, 57(2), 2001, pp. 368-368
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:
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:
Lampe, J
Kitzler, H
Walter, MC
Lochmuller, H
Reichmann, H
Citation: J. Lampe et al., Methionine homozygosity at prion gene codon 129 may predispose to sporadicinclusion-body myositis, LANCET, 353(9151), 1999, pp. 465-466
Risultati:
1-7
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