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Stephan Zierz

Showing results (81-90 of 123) with videos related to

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Neuromuscular Disorders : NMD|March 29, 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Gavin Hudson, Tobias Müller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 22, 2014
SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletionsFrank Hanisch, Malte Kornhuber, Charlotte L Alston, et al.
European Cytokine Network|January 9, 2003
Energetic depression caused by mitochondrial dysfunctionFrank Norbert Gellerich, Sonata Trumbeckaite, Ying Chen, et al.
Life (Basel, Switzerland)|September 19, 2020
Palmitate but Not Oleate Exerts a Negative Effect on Oxygen Utilization in Myoblasts of Patients with the m.3243A>G Mutation: A Pilot StudyLeila Motlagh Scholle, Helena Schieffers, Samiya Al-Robaiy, et al.
Mitochondrion|January 1, 2018
Cognitive impairment, clinical severity and MRI changes in MELAS syndromeTorsten Kraya, Lena Neumann, Yvonne Paelecke-Habermann, et al.
Journal of Neurology|February 18, 2016
Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophyMarius Kuhn, Dieter Gläser, Pushpa Raj Joshi, et al.
Molecular and Cellular Biochemistry|February 24, 2004
Energetic depression caused by mitochondrial dysfunctionFrank Norbert Gellerich, Sonata Trumbeckaite, Tobias Müller, et al.
Archives of Neurology|January 21, 2003
Increased metabolic muscle fatigue is caused by some but not all mitochondrial mutationsWilhelm J Schulte-Mattler, Tobias Müller, Marcus Deschauer, et al.
Journal of Neurology|September 26, 2012
Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation studyKai Boelmans, Jörn Kaufmann, Sophie Schmelzer, et al.
Neuromuscular Disorders : NMD|August 19, 2003
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Reinhard Kiefer, Emma L Blakely, et al.
Pageof 13

Showing results (81-90 of 123) with videos related to

Sort By:
Pageof 13
Neuromuscular Disorders : NMD|March 29, 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Gavin Hudson, Tobias Müller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 22, 2014
SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletionsFrank Hanisch, Malte Kornhuber, Charlotte L Alston, et al.
European Cytokine Network|January 9, 2003
Energetic depression caused by mitochondrial dysfunctionFrank Norbert Gellerich, Sonata Trumbeckaite, Ying Chen, et al.
Life (Basel, Switzerland)|September 19, 2020
Palmitate but Not Oleate Exerts a Negative Effect on Oxygen Utilization in Myoblasts of Patients with the m.3243A>G Mutation: A Pilot StudyLeila Motlagh Scholle, Helena Schieffers, Samiya Al-Robaiy, et al.
Mitochondrion|January 1, 2018
Cognitive impairment, clinical severity and MRI changes in MELAS syndromeTorsten Kraya, Lena Neumann, Yvonne Paelecke-Habermann, et al.
Journal of Neurology|February 18, 2016
Utility of a next-generation sequencing-based gene panel investigation in German patients with genetically unclassified limb-girdle muscular dystrophyMarius Kuhn, Dieter Gläser, Pushpa Raj Joshi, et al.
Molecular and Cellular Biochemistry|February 24, 2004
Energetic depression caused by mitochondrial dysfunctionFrank Norbert Gellerich, Sonata Trumbeckaite, Tobias Müller, et al.
Archives of Neurology|January 21, 2003
Increased metabolic muscle fatigue is caused by some but not all mitochondrial mutationsWilhelm J Schulte-Mattler, Tobias Müller, Marcus Deschauer, et al.
Journal of Neurology|September 26, 2012
Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation studyKai Boelmans, Jörn Kaufmann, Sophie Schmelzer, et al.
Neuromuscular Disorders : NMD|August 19, 2003
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Reinhard Kiefer, Emma L Blakely, et al.
Pageof 13