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Cornelia Kornblum

Showing results (1-10 of 77) with videos related to

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Journal of Neuromuscular Diseases|August 11, 2020
Towards Central Nervous System Involvement in Adults with Hereditary MyopathiesJens Reimann, Cornelia Kornblum
Handbook of Clinical Neurology|February 22, 2023
Currently available therapies in mitochondrial diseaseCornelia Kornblum, Costanza Lamperti, Sumit Parikh
Frontiers in Neurology|September 7, 2018
Current Progress in CNS Imaging of Myotonic DystrophyMartina Minnerop, Carla Gliem, Cornelia Kornblum
Neuromuscular Disorders : NMD|April 24, 2025
280th ENMC International Workshop: The ERN EURO-NMD mitochondrial diseases working group; diagnostic criteria and outcome measures in primary mitochondrial myopathies. Hoofddorp, the Netherlands, 22-24 November 2024Michelangelo Mancuso, Piervito Lopriore, Luisa Semmler, et al.
Brain : a Journal of Neurology|April 12, 2003
Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndromeSimone Bosbach, Cornelia Kornblum, Rolf Schröder, et al.
Muscle & Nerve|January 9, 2007
Variability of the recessive oculopharyngeal muscular dystrophy phenotypeAlexander Semmler, Wolfram Kress, Stefan Vielhaber, et al.
Neuromuscular Disorders : NMD|February 5, 2022
Long-term effects of enzyme replacement therapy in an elderly cohort of late-onset Pompe diseaseMaren Winkler, Christina von Landenberg, Katharina Kuchenbecker, et al.
Clinical and Experimental Rheumatology|January 21, 2026
The MicroIBioM study: the gut microbiome in inclusion body myositisMaren Winkler, Waldemar Seel, Cornelia Kornblum, et al.
Journal of Neuromuscular Diseases|August 30, 2021
Early Changes in Skeletal Muscle of Young C22 Mice, A Model of Charcot-Marie-Tooth 1AFriederike Deres, Stephanie Schwartz, Karin Kappes-Horn, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 3, 2005
Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosisThorsten Okulla, Wolfram S Kunz, Thomas Klockgether, et al.
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
Journal of Neuromuscular Diseases|August 11, 2020
Towards Central Nervous System Involvement in Adults with Hereditary MyopathiesJens Reimann, Cornelia Kornblum
Handbook of Clinical Neurology|February 22, 2023
Currently available therapies in mitochondrial diseaseCornelia Kornblum, Costanza Lamperti, Sumit Parikh
Frontiers in Neurology|September 7, 2018
Current Progress in CNS Imaging of Myotonic DystrophyMartina Minnerop, Carla Gliem, Cornelia Kornblum
Neuromuscular Disorders : NMD|April 24, 2025
280th ENMC International Workshop: The ERN EURO-NMD mitochondrial diseases working group; diagnostic criteria and outcome measures in primary mitochondrial myopathies. Hoofddorp, the Netherlands, 22-24 November 2024Michelangelo Mancuso, Piervito Lopriore, Luisa Semmler, et al.
Brain : a Journal of Neurology|April 12, 2003
Executive and visuospatial deficits in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndromeSimone Bosbach, Cornelia Kornblum, Rolf Schröder, et al.
Muscle & Nerve|January 9, 2007
Variability of the recessive oculopharyngeal muscular dystrophy phenotypeAlexander Semmler, Wolfram Kress, Stefan Vielhaber, et al.
Neuromuscular Disorders : NMD|February 5, 2022
Long-term effects of enzyme replacement therapy in an elderly cohort of late-onset Pompe diseaseMaren Winkler, Christina von Landenberg, Katharina Kuchenbecker, et al.
Clinical and Experimental Rheumatology|January 21, 2026
The MicroIBioM study: the gut microbiome in inclusion body myositisMaren Winkler, Waldemar Seel, Cornelia Kornblum, et al.
Journal of Neuromuscular Diseases|August 30, 2021
Early Changes in Skeletal Muscle of Young C22 Mice, A Model of Charcot-Marie-Tooth 1AFriederike Deres, Stephanie Schwartz, Karin Kappes-Horn, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 3, 2005
Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosisThorsten Okulla, Wolfram S Kunz, Thomas Klockgether, et al.
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