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M C Walter

Showing results (31-40 of 45) with videos related to

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Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 15, 2009
Phenotypic variability in siblings with calpainopathy (LGMD2A)J Schessl, M C Walter, G Schreiber, 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 Neurology|March 22, 2008
No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutationsL E Hjermind, J Vissing, F Asmus, et al.
Journal of Neuromuscular Diseases|June 16, 2020
Measuring Outcomes in Adults with Spinal Muscular Atrophy - Challenges and Future Directions - Meeting ReportV A Sansone, M C Walter, S Attarian, 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.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 30, 2005
Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutationsD Brummer, M C Walter, M Palmbach, 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.
Brain : a Journal of Neurology|November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescueD Hicks, A K Lampe, S H Laval, 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.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 15, 2009
Phenotypic variability in siblings with calpainopathy (LGMD2A)J Schessl, M C Walter, G Schreiber, 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 Neurology|March 22, 2008
No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutationsL E Hjermind, J Vissing, F Asmus, et al.
Journal of Neuromuscular Diseases|June 16, 2020
Measuring Outcomes in Adults with Spinal Muscular Atrophy - Challenges and Future Directions - Meeting ReportV A Sansone, M C Walter, S Attarian, 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.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 30, 2005
Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutationsD Brummer, M C Walter, M Palmbach, 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.
Brain : a Journal of Neurology|November 19, 2008
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescueD Hicks, A K Lampe, S H Laval, 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.
Pageof 5