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Stephan Zierz

Showing results (111-120 of 123) with videos related to

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Journal of Neuromuscular Diseases|June 13, 2022
GFPT1-Associated Congenital Myasthenic Syndrome Mimicking a Glycogen Storage Disease - Diagnostic Pitfalls in Myopathology Solved by Next-Generation-SequencingAlexander Mensch, Isabell Cordts, Leila Scholle, et al.
Experimental and Clinical Cardiology|July 31, 2009
Intracellular energetic units in healthy and diseased heartsEnn K Seppet, Margus Eimre, Tiia Anmann, et al.
Journal of Neurology|April 14, 2009
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosisRubén Fernández-Santiago, Sabine Hoenig, Peter Lichtner, et al.
Acta Neurologica Scandinavica|November 19, 2016
The concept and diagnostic criteria of primary lateral sclerosisVerena Wais, Angela Rosenbohm, Susanne Petri, et al.
Journal of Neurology|March 4, 2024
Quantitative whole-body muscle MRI in idiopathic inflammatory myopathies including polymyositis with mitochondrial pathology: indications for a disease spectrumLea-Katharina Zierer, Steffen Naegel, Ilka Schneider, et al.
International Journal of Molecular Sciences|July 1, 2009
Mitochondria and energetic depression in cell pathophysiologyEnn Seppet, Marju Gruno, Ants Peetsalu, et al.
Nucleic Acids Research|June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre levelDiana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 23, 2024
A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disordersAmy E Vincent, Chun Chen, Tiago Bernardino Gomes, et al.
Plos One|June 21, 2012
A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosisLuc Dupuis, Reinhard Dengler, Michael T Heneka, et al.
Neurology|May 13, 2016
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weaknessZoltan Lukacs, Paulina Nieves Cobos, Stephan Wenninger, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
Journal of Neuromuscular Diseases|June 13, 2022
GFPT1-Associated Congenital Myasthenic Syndrome Mimicking a Glycogen Storage Disease - Diagnostic Pitfalls in Myopathology Solved by Next-Generation-SequencingAlexander Mensch, Isabell Cordts, Leila Scholle, et al.
Experimental and Clinical Cardiology|July 31, 2009
Intracellular energetic units in healthy and diseased heartsEnn K Seppet, Margus Eimre, Tiia Anmann, et al.
Journal of Neurology|April 14, 2009
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosisRubén Fernández-Santiago, Sabine Hoenig, Peter Lichtner, et al.
Acta Neurologica Scandinavica|November 19, 2016
The concept and diagnostic criteria of primary lateral sclerosisVerena Wais, Angela Rosenbohm, Susanne Petri, et al.
Journal of Neurology|March 4, 2024
Quantitative whole-body muscle MRI in idiopathic inflammatory myopathies including polymyositis with mitochondrial pathology: indications for a disease spectrumLea-Katharina Zierer, Steffen Naegel, Ilka Schneider, et al.
International Journal of Molecular Sciences|July 1, 2009
Mitochondria and energetic depression in cell pathophysiologyEnn Seppet, Marju Gruno, Ants Peetsalu, et al.
Nucleic Acids Research|June 1, 2019
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre levelDiana Lehmann, Helen A L Tuppen, Georgia E Campbell, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 23, 2024
A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disordersAmy E Vincent, Chun Chen, Tiago Bernardino Gomes, et al.
Plos One|June 21, 2012
A randomized, double blind, placebo-controlled trial of pioglitazone in combination with riluzole in amyotrophic lateral sclerosisLuc Dupuis, Reinhard Dengler, Michael T Heneka, et al.
Neurology|May 13, 2016
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weaknessZoltan Lukacs, Paulina Nieves Cobos, Stephan Wenninger, et al.
Pageof 13