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Matthias Vorgerd

Showing results (61-70 of 140) with videos related to

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European Journal of Neurology|September 16, 2024
Pre- and post-skeletal muscle biopsy quantitative magnetic resonance imaging reveals correlations with histopathological findingsAnne-Katrin Güttsches, Johannes Forsting, Moritz Kneifel, et al.
Journal of Human Genetics|October 19, 2006
Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and TurkeyYoriko Endo, Asako Horinishi, Matthias Vorgerd, et al.
Neuromuscular Disorders : NMD|March 6, 2015
Two novel nebulin variants in an adult patient with congenital nemaline myopathyAnne K Güttsches, Gabriele Dekomien, Kristl G Claeys, et al.
Frontiers in Neuroscience|August 30, 2017
Treadmill Training with HAL Exoskeleton-A Novel Approach for Symptomatic Therapy in Patients with Limb-Girdle Muscular Dystrophy-Preliminary StudyMatthias Sczesny-Kaiser, Rebecca Kowalewski, Thomas A Schildhauer, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of casesBarbara Burwinkel, Bin Hu, Anja Schroers, et al.
Neuromuscular Disorders : NMD|May 9, 2015
50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutationMaggie C Walter, Martina Rossius, Manuela Zitzelsberger, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Muscle imaging data in late-onset Pompe disease reveal a correlation between the pre-existing degree of lipomatous muscle alterations and the efficacy of long-term enzyme replacement therapyKai Michael Gruhn, Christoph Malte Heyer, Anne-Katrin Güttsches, et al.
Journal of Clinical Medicine|April 13, 2024
Evaluation of Neuromuscular Diseases and Complaints by Quantitative Muscle MRILara Schlaffke, Robert Rehmann, Anne-Katrin Güttsches, et al.
Stem Cells International|November 29, 2023
CRISPR/Cas9 Genome Editing in LGMD2A/R1 Patient-Derived Induced Pluripotent Stem and Skeletal Muscle Progenitor CellsLampros Mavrommatis, Abdul Zaben, Urs Kindler, et al.
European Journal of Haematology|August 24, 2010
Diagnosis of leptomeningeal disease in diffuse large B-cell lymphomas of the central nervous system by flow cytometry and cytopathologyRoland Schroers, Alexander Baraniskin, Christoph Heute, et al.
Pageof 14

Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
European Journal of Neurology|September 16, 2024
Pre- and post-skeletal muscle biopsy quantitative magnetic resonance imaging reveals correlations with histopathological findingsAnne-Katrin Güttsches, Johannes Forsting, Moritz Kneifel, et al.
Journal of Human Genetics|October 19, 2006
Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and TurkeyYoriko Endo, Asako Horinishi, Matthias Vorgerd, et al.
Neuromuscular Disorders : NMD|March 6, 2015
Two novel nebulin variants in an adult patient with congenital nemaline myopathyAnne K Güttsches, Gabriele Dekomien, Kristl G Claeys, et al.
Frontiers in Neuroscience|August 30, 2017
Treadmill Training with HAL Exoskeleton-A Novel Approach for Symptomatic Therapy in Patients with Limb-Girdle Muscular Dystrophy-Preliminary StudyMatthias Sczesny-Kaiser, Rebecca Kowalewski, Thomas A Schildhauer, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of casesBarbara Burwinkel, Bin Hu, Anja Schroers, et al.
Neuromuscular Disorders : NMD|May 9, 2015
50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutationMaggie C Walter, Martina Rossius, Manuela Zitzelsberger, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Muscle imaging data in late-onset Pompe disease reveal a correlation between the pre-existing degree of lipomatous muscle alterations and the efficacy of long-term enzyme replacement therapyKai Michael Gruhn, Christoph Malte Heyer, Anne-Katrin Güttsches, et al.
Journal of Clinical Medicine|April 13, 2024
Evaluation of Neuromuscular Diseases and Complaints by Quantitative Muscle MRILara Schlaffke, Robert Rehmann, Anne-Katrin Güttsches, et al.
Stem Cells International|November 29, 2023
CRISPR/Cas9 Genome Editing in LGMD2A/R1 Patient-Derived Induced Pluripotent Stem and Skeletal Muscle Progenitor CellsLampros Mavrommatis, Abdul Zaben, Urs Kindler, et al.
European Journal of Haematology|August 24, 2010
Diagnosis of leptomeningeal disease in diffuse large B-cell lymphomas of the central nervous system by flow cytometry and cytopathologyRoland Schroers, Alexander Baraniskin, Christoph Heute, et al.
Pageof 14