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M Deschauer

Showing results (1-10 of 37) with videos related to

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Zeitschrift Fur Rheumatologie|April 5, 2013
[Metabolic and mitochondrial myopathies]M Vorgerd, M Deschauer
Der Nervenarzt|March 26, 2004
["Seronegative" myasthenia with antibodies against muscle-specific tyrosine-kinase]B Hain, F Hanisch, M Deschauer
Fortschritte Der Neurologie-Psychiatrie|May 5, 1998
[Hearing loss as the leading symptom in anterior inferior cerebellar artery infarction]M Deschauer, D Georgiadis, A Lindner
Klinische Monatsblatter Fur Augenheilkunde|October 16, 2009
[Chronic progressive external ophthalmoplegia--symptom or syndrome?]V Bau, M Deschauer, S Zierz
Der Nervenarzt|March 21, 2001
[Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with differing genetics]M Deschauer, T Müller, S Dreha, et al.
Der Nervenarzt|June 29, 2004
[The clinical spectrum of limb-girdle muscular dystrophies type 2I in cases of a mutation in the "fukutin-related- protein"-gene]M Krasnianski, S Neudecker, M Deschauer, et al.
Molecular Genetics and Metabolism|December 26, 2001
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle diseaseM Deschauer, J R Opalka, A Lindner, et al.
Journal of Neurology|April 19, 2006
Genetic heterogeneity in 30 German patients with oculopharyngeal muscular dystrophyT Müller, M Deschauer, F Kolbe-Fehr, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutationT Müller, M Krasnianski, R Witthaut, et al.
Neurology|April 23, 2003
Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patientsT Wieser, M Deschauer, K Olek, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Zeitschrift Fur Rheumatologie|April 5, 2013
[Metabolic and mitochondrial myopathies]M Vorgerd, M Deschauer
Der Nervenarzt|March 26, 2004
["Seronegative" myasthenia with antibodies against muscle-specific tyrosine-kinase]B Hain, F Hanisch, M Deschauer
Fortschritte Der Neurologie-Psychiatrie|May 5, 1998
[Hearing loss as the leading symptom in anterior inferior cerebellar artery infarction]M Deschauer, D Georgiadis, A Lindner
Klinische Monatsblatter Fur Augenheilkunde|October 16, 2009
[Chronic progressive external ophthalmoplegia--symptom or syndrome?]V Bau, M Deschauer, S Zierz
Der Nervenarzt|March 21, 2001
[Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with differing genetics]M Deschauer, T Müller, S Dreha, et al.
Der Nervenarzt|June 29, 2004
[The clinical spectrum of limb-girdle muscular dystrophies type 2I in cases of a mutation in the "fukutin-related- protein"-gene]M Krasnianski, S Neudecker, M Deschauer, et al.
Molecular Genetics and Metabolism|December 26, 2001
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle diseaseM Deschauer, J R Opalka, A Lindner, et al.
Journal of Neurology|April 19, 2006
Genetic heterogeneity in 30 German patients with oculopharyngeal muscular dystrophyT Müller, M Deschauer, F Kolbe-Fehr, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutationT Müller, M Krasnianski, R Witthaut, et al.
Neurology|April 23, 2003
Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patientsT Wieser, M Deschauer, K Olek, et al.
Pageof 4