Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jens Reimann

Showing results (41-50 of 56) with videos related to

Pageof 6
Sort By:
Journal of Neurology|May 6, 2011
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 genePeter Reilich, Rita Horvath, Sabine Krause, et al.
Nature Communications|April 11, 2026
Blockage of autophagy causes severe skeletal muscle disruption in a mouse model for myofibrillar myopathy 6Kerstin Filippi, Kathrin Graf-Riesen, Maithreyan Kuppusamy, et al.
Brain : a Journal of Neurology|September 14, 2010
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseasesChristoph S Clemen, Karthikeyan Tangavelou, Karl-Heinz Strucksberg, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2002
Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophyRolf Schröder, Wolfram S Kunz, Fatima Rouan, et al.
Der Nervenarzt|April 29, 2024
[Expert recommendations for magnetic resonance imaging of muscle disorders]Rachel Zeng, Sarah Schlaeger, Matthias Türk, et al.
Radiologie (Heidelberg, Germany)|April 19, 2024
[Expert recommendations for magnetic resonance imaging of muscle disorders]Rachel Zeng, Sarah Schlaeger, Matthias Türk, et al.
European Journal of Neurology|August 16, 2022
European Neuromuscular Centre consensus statement on anaesthesia in patients with neuromuscular disordersLuuk R van den Bersselaar, Luc Heytens, Helga C A Silva, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Brain : a Journal of Neurology|September 21, 2006
Pathological consequences of VCP mutations on human striated muscleChristian U Hübbers, Christoph S Clemen, Kristina Kesper, et al.
Orphanet Journal of Rare Diseases|May 12, 2017
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 casesLukas J Schnitzler, Tobias Schreckenbach, Aleksandra Nadaj-Pakleza, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Journal of Neurology|May 6, 2011
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 genePeter Reilich, Rita Horvath, Sabine Krause, et al.
Nature Communications|April 11, 2026
Blockage of autophagy causes severe skeletal muscle disruption in a mouse model for myofibrillar myopathy 6Kerstin Filippi, Kathrin Graf-Riesen, Maithreyan Kuppusamy, et al.
Brain : a Journal of Neurology|September 14, 2010
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseasesChristoph S Clemen, Karthikeyan Tangavelou, Karl-Heinz Strucksberg, et al.
Journal of Neuropathology and Experimental Neurology|June 20, 2002
Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophyRolf Schröder, Wolfram S Kunz, Fatima Rouan, et al.
Der Nervenarzt|April 29, 2024
[Expert recommendations for magnetic resonance imaging of muscle disorders]Rachel Zeng, Sarah Schlaeger, Matthias Türk, et al.
Radiologie (Heidelberg, Germany)|April 19, 2024
[Expert recommendations for magnetic resonance imaging of muscle disorders]Rachel Zeng, Sarah Schlaeger, Matthias Türk, et al.
European Journal of Neurology|August 16, 2022
European Neuromuscular Centre consensus statement on anaesthesia in patients with neuromuscular disordersLuuk R van den Bersselaar, Luc Heytens, Helga C A Silva, et al.
Acta Neuropathologica|May 11, 2021
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusionsMridul Johari, Jaakko Sarparanta, Anna Vihola, et al.
Brain : a Journal of Neurology|September 21, 2006
Pathological consequences of VCP mutations on human striated muscleChristian U Hübbers, Christoph S Clemen, Kristina Kesper, et al.
Orphanet Journal of Rare Diseases|May 12, 2017
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 casesLukas J Schnitzler, Tobias Schreckenbach, Aleksandra Nadaj-Pakleza, et al.
Pageof 6