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G Schoser

Showing results (21-30 of 29) with videos related to

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Human Molecular Genetics|April 21, 2006
DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expressionJamie M Margolis, Benedikt G Schoser, Melinda L Moseley, et al.
Journal of Medical Genetics|June 3, 2004
Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III geneR Horváth, H Lochmüller, M Hoeltzenbein, et al.
Brain : a Journal of Neurology|May 20, 2005
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophiesAnna Krasnianski, Marcus Deschauer, Stephan Neudecker, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Brain : a Journal of Neurology|December 7, 2007
McLeod myopathy revisited: more neurogenic and less benignEkkehard Hewer, Adrian Danek, Benedikt G Schoser, et al.
Journal of Medical Genetics|October 22, 2003
A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophyR Horváth, H Lochmüller, C Scharfe, 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.
Histochemistry and Cell Biology|July 10, 2016
Differential expression and localization of Ankrd2 isoforms in human skeletal and cardiac musclesJovana Jasnic-Savovic, Sabine Krause, Slobodan Savic, et al.
Nature Genetics|June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Human Molecular Genetics|April 21, 2006
DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expressionJamie M Margolis, Benedikt G Schoser, Melinda L Moseley, et al.
Journal of Medical Genetics|June 3, 2004
Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III geneR Horváth, H Lochmüller, M Hoeltzenbein, et al.
Brain : a Journal of Neurology|May 20, 2005
Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophiesAnna Krasnianski, Marcus Deschauer, Stephan Neudecker, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Brain : a Journal of Neurology|December 7, 2007
McLeod myopathy revisited: more neurogenic and less benignEkkehard Hewer, Adrian Danek, Benedikt G Schoser, et al.
Journal of Medical Genetics|October 22, 2003
A tRNA(Ala) mutation causing mitochondrial myopathy clinically resembling myotonic dystrophyR Horváth, H Lochmüller, C Scharfe, 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.
Histochemistry and Cell Biology|July 10, 2016
Differential expression and localization of Ankrd2 isoforms in human skeletal and cardiac musclesJovana Jasnic-Savovic, Sabine Krause, Slobodan Savic, et al.
Nature Genetics|June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.
Pageof 3