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Jens Reimann

Showing results (21-30 of 56) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 27, 2005
The oral antidiabetic pioglitazone protects from neurodegeneration and amyotrophic lateral sclerosis-like symptoms in superoxide dismutase-G93A transgenic miceBurkhard Schütz, Jens Reimann, Lucia Dumitrescu-Ozimek, et al.
Neurology|August 8, 2013
Diagnostic challenge and therapeutic dilemma in necrotizing myopathyKristl G Claeys, Olga Gorodinskaya, Susanne Handt, et al.
Neuromuscular Disorders : NMD|March 23, 2010
Reverse protein arrays as novel approach for protein quantification in muscular dystrophiesClaudia Escher, Hanns Lochmüller, Dirk Fischer, et al.
Clinical Neuropathology|June 3, 2014
Clinical and morphological variability of the E396K mutation in the neurofilament light chain gene in patients with Charcot-Marie- Tooth disease type 2EMiriam Elbracht, Jan Senderek, Ulrike Schara, et al.
Human Molecular Genetics|April 18, 2023
Extension of the DNAJB2a isoform in a dominant neuromyopathy familyJaakko Sarparanta, Per Harald Jonson, Jens Reimann, et al.
Neurology. Genetics|April 12, 2017
Camptocormia and shuffling gait due to a novel <i>MT-TV</i> mutation: Diagnostic pitfallsJens Reimann, Diana Lehmann, Steven A Hardy, et al.
Epilepsy & Behavior : E&B|December 15, 2010
Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgeryPitt Niehusmann, Rainer Surges, Randi D von Wrede, et al.
Journal of Neurology|November 28, 2025
Characterization of novel CASQ1 variants in two families with unusual phenotypic featuresMilla Laarne, Manu Jokela, Fang Zhao, et al.
Orphanet Journal of Rare Diseases|February 12, 2026
Myopathy and ataxia related to impaired mitochondrial function in mevalonate kinase deficiencyAlessia Pugliese, Christina von Landenberg, Romina Gallizzi, et al.
Ophthalmology. Retina|July 14, 2021
Mitochondrial RetinopathyJohannes Birtel, Christina von Landenberg, Martin Gliem, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 27, 2005
The oral antidiabetic pioglitazone protects from neurodegeneration and amyotrophic lateral sclerosis-like symptoms in superoxide dismutase-G93A transgenic miceBurkhard Schütz, Jens Reimann, Lucia Dumitrescu-Ozimek, et al.
Neurology|August 8, 2013
Diagnostic challenge and therapeutic dilemma in necrotizing myopathyKristl G Claeys, Olga Gorodinskaya, Susanne Handt, et al.
Neuromuscular Disorders : NMD|March 23, 2010
Reverse protein arrays as novel approach for protein quantification in muscular dystrophiesClaudia Escher, Hanns Lochmüller, Dirk Fischer, et al.
Clinical Neuropathology|June 3, 2014
Clinical and morphological variability of the E396K mutation in the neurofilament light chain gene in patients with Charcot-Marie- Tooth disease type 2EMiriam Elbracht, Jan Senderek, Ulrike Schara, et al.
Human Molecular Genetics|April 18, 2023
Extension of the DNAJB2a isoform in a dominant neuromyopathy familyJaakko Sarparanta, Per Harald Jonson, Jens Reimann, et al.
Neurology. Genetics|April 12, 2017
Camptocormia and shuffling gait due to a novel <i>MT-TV</i> mutation: Diagnostic pitfallsJens Reimann, Diana Lehmann, Steven A Hardy, et al.
Epilepsy & Behavior : E&B|December 15, 2010
Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgeryPitt Niehusmann, Rainer Surges, Randi D von Wrede, et al.
Journal of Neurology|November 28, 2025
Characterization of novel CASQ1 variants in two families with unusual phenotypic featuresMilla Laarne, Manu Jokela, Fang Zhao, et al.
Orphanet Journal of Rare Diseases|February 12, 2026
Myopathy and ataxia related to impaired mitochondrial function in mevalonate kinase deficiencyAlessia Pugliese, Christina von Landenberg, Romina Gallizzi, et al.
Ophthalmology. Retina|July 14, 2021
Mitochondrial RetinopathyJohannes Birtel, Christina von Landenberg, Martin Gliem, et al.
Pageof 6