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Stephan Zierz

Showing results (101-110 of 123) with videos related to

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Muscle & Nerve|October 14, 2014
Histological characterization and biochemical analysis of paraspinal muscles in neuromuscularly healthy subjectsClaudia Zimmermann, Rajakiran Kalepu, Matthias Ponfick, et al.
Journal of Neurology|December 26, 2015
Clinical features and differential diagnosis of flail arm syndromeAnnemarie Hübers, Viviane Hildebrandt, Susanne Petri, et al.
Annals of Neurology|August 27, 2014
Phenotype of matrin-3-related distal myopathy in 16 German patientsTobias J Müller, Torsten Kraya, Gisela Stoltenburg-Didinger, et al.
The Journal of Biological Chemistry|July 9, 2008
Impaired regulation of brain mitochondria by extramitochondrial Ca2+ in transgenic Huntington disease ratsFrank N Gellerich, Zemfira Gizatullina, Huu P Nguyen, et al.
Annals of Neurology|January 27, 2006
Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 miceZemfira Z Gizatullina, Katrin S Lindenberg, Phoebe Harjes, et al.
Experimental Neurology|June 7, 2015
HMGB1 and RAGE in skeletal muscle inflammation: Implications for protein accumulation in inclusion body myositisIngrid E Muth, Jana Zschüntzsch, Konstanze Kleinschnitz, et al.
Journal of Clinical Neuromuscular Disease|November 26, 2024
A Novel MYH14 Variant Presenting as a New Phenotype of MYH14-Associated Neuromuscular Disorders-Clinicohistologic Findings and Review of the LiteratureAlexander Mensch, Berit Jordan, Joachim Weis, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophyMichal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Molecular and Cellular Biochemistry|March 29, 2005
Compartmentation of energy metabolism in atrial myocardium of patients undergoing cardiac surgeryEvelin Seppet, Margus Eimre, Nadezhda Peet, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathyDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Pageof 13

Showing results (101-110 of 123) with videos related to

Sort By:
Pageof 13
Muscle & Nerve|October 14, 2014
Histological characterization and biochemical analysis of paraspinal muscles in neuromuscularly healthy subjectsClaudia Zimmermann, Rajakiran Kalepu, Matthias Ponfick, et al.
Journal of Neurology|December 26, 2015
Clinical features and differential diagnosis of flail arm syndromeAnnemarie Hübers, Viviane Hildebrandt, Susanne Petri, et al.
Annals of Neurology|August 27, 2014
Phenotype of matrin-3-related distal myopathy in 16 German patientsTobias J Müller, Torsten Kraya, Gisela Stoltenburg-Didinger, et al.
The Journal of Biological Chemistry|July 9, 2008
Impaired regulation of brain mitochondria by extramitochondrial Ca2+ in transgenic Huntington disease ratsFrank N Gellerich, Zemfira Gizatullina, Huu P Nguyen, et al.
Annals of Neurology|January 27, 2006
Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 miceZemfira Z Gizatullina, Katrin S Lindenberg, Phoebe Harjes, et al.
Experimental Neurology|June 7, 2015
HMGB1 and RAGE in skeletal muscle inflammation: Implications for protein accumulation in inclusion body myositisIngrid E Muth, Jana Zschüntzsch, Konstanze Kleinschnitz, et al.
Journal of Clinical Neuromuscular Disease|November 26, 2024
A Novel MYH14 Variant Presenting as a New Phenotype of MYH14-Associated Neuromuscular Disorders-Clinicohistologic Findings and Review of the LiteratureAlexander Mensch, Berit Jordan, Joachim Weis, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophyMichal Vytopil, Enzo Ricci, Antonio Dello Russo, et al.
Molecular and Cellular Biochemistry|March 29, 2005
Compartmentation of energy metabolism in atrial myocardium of patients undergoing cardiac surgeryEvelin Seppet, Margus Eimre, Nadezhda Peet, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathyDiana Lehmann, Kathrin Schubert, Pushpa R Joshi, et al.
Pageof 13