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H Goebel

Showing results (421-430 of 483) with videos related to

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Neuromuscular Disorders : NMD|January 5, 2000
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravisW Müller-Felber, C F Ansevin, K Ricker, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
European Surgical Research. Europaische Chirurgische Forschung. Recherches Chirurgicales Europeennes|November 2, 2005
Development of a special balloon occlusion device to prevent adverse events in high-risk patients during open aortic surgeryE Weigang, M Luehr, P von Samson, et al.
Neuromuscular Disorders : NMD|September 14, 2010
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studiesA L Taratuto, H O Akman, M Saccoliti, et al.
Human Mutation|December 24, 2008
How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathyChristoph S Clemen, Dirk Fischer, Jens Reimann, et al.
Muscle & Nerve|September 1, 1997
Spheroid body myopathy revisitedH H Goebel, A N D'Agostino, J Wilson, et al.
The American Journal of Pathology|October 13, 2012
Immune-mediated necrotizing myopathy is characterized by a specific Th1-M1 polarized immune profileCorinna Preuße, Hans H Goebel, Josephin Held, et al.
Neurology|December 30, 2004
T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndromeI Harting, A Blaschek, N I Wolf, et al.
Muscle & Nerve|August 10, 2013
Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expressionNicolas W J Schröder, Ulrike Grieben, Stefan Prokop, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Pageof 49

Showing results (421-430 of 483) with videos related to

Sort By:
Pageof 49
Neuromuscular Disorders : NMD|January 5, 2000
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravisW Müller-Felber, C F Ansevin, K Ricker, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
European Surgical Research. Europaische Chirurgische Forschung. Recherches Chirurgicales Europeennes|November 2, 2005
Development of a special balloon occlusion device to prevent adverse events in high-risk patients during open aortic surgeryE Weigang, M Luehr, P von Samson, et al.
Neuromuscular Disorders : NMD|September 14, 2010
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studiesA L Taratuto, H O Akman, M Saccoliti, et al.
Human Mutation|December 24, 2008
How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathyChristoph S Clemen, Dirk Fischer, Jens Reimann, et al.
Muscle & Nerve|September 1, 1997
Spheroid body myopathy revisitedH H Goebel, A N D'Agostino, J Wilson, et al.
The American Journal of Pathology|October 13, 2012
Immune-mediated necrotizing myopathy is characterized by a specific Th1-M1 polarized immune profileCorinna Preuße, Hans H Goebel, Josephin Held, et al.
Neurology|December 30, 2004
T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndromeI Harting, A Blaschek, N I Wolf, et al.
Muscle & Nerve|August 10, 2013
Novel γ-sarcoglycan-mutation affects cardiac function and N-terminal dystrophin expressionNicolas W J Schröder, Ulrike Grieben, Stefan Prokop, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Pageof 49