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Der Nervenarzt|March 21, 2001
[New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)]M C Walter, H Lochmüller, B Schlotter, et al.
Journal of Neurology|March 4, 2000
High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled studyM C Walter, H Lochmüller, M Toepfer, et al.
Neurology|May 10, 2000
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical studyM C Walter, H Lochmüller, P Reilich, et al.
Neuromuscular Disorders : NMD|December 7, 2002
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathyH J Durling, P Reilich, J Müller-Höcker, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 10, 2004
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthoodM C Walter, G Dekomien, B Schlotter-Weigel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 19, 2015
Alterations in the trapezius muscle in young patients with migraine--a pilot case series with MRIM N Landgraf, B Ertl-Wagner, I K Koerte, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 3, 2008
LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filamentsP Reilich, J A Petersen, S Vielhaber, et al.
Clinical Neuropathology|October 3, 2007
Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing proteinS Krause, T Göhringer, M C Walter, et al.
Neuropediatrics|November 7, 2012
Ten-year follow-up in a case series of integrative botulinum toxin intervention in adolescents with chronic daily headache and associated muscle painA S Schroeder, K Huss, A Blaschek, et al.
Brain : a Journal of Neurology|April 19, 2007
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350PM C Walter, P Reilich, A Huebner, et al.
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