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Matthias Vorgerd

Showing results (131-140 of 140) with videos related to

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Brain : a Journal of Neurology|December 7, 2007
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patientsRudolf A Kley, Yorck Hellenbroich, Peter F M van der Ven, et al.
Nature Communications|September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe diseaseLina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Brain : a Journal of Neurology|January 18, 2021
Bi-allelic truncating mutations in VWA1 cause neuromyopathyMarcus Deschauer, Holger Hengel, Katrin Rupprich, et al.
Elife|November 14, 2023
Human skeletal muscle organoids model fetal myogenesis and sustain uncommitted PAX7 myogenic progenitorsLampros Mavrommatis, Hyun-Woo Jeong, Urs Kindler, et al.
Biochemical and Biophysical Research Communications|August 14, 2018
The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?Christoph S Clemen, Lilli Winter, Karl-Heinz Strucksberg, et al.
Histology and Histopathology|March 13, 2013
Morphological spectrum and clinical features of myopathies with tubular aggregatesFabian Funk, Chantal Ceuterick-de Groote, Jean-Jacques Martin, et al.
Journal of Neurology|March 9, 2023
Periostin as a blood biomarker of muscle cell fibrosis, cardiomyopathy and disease severity in myotonic dystrophy type 1Chi D L Nguyen, Aura Cecilia Jimenez-Moreno, Monika Merker, et al.
Brain : a Journal of Neurology|May 10, 2023
Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defectsAndreas Roos, Peter F M van der Ven, Hadil Alrohaif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2022
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre studyMarianela Schiava, Chiseko Ikenaga, Rocío Nur Villar-Quiles, et al.
Neurology. Genetics|July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem ProteinopathyMarianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Pageof 14

Showing results (131-140 of 140) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 140 results.
Brain : a Journal of Neurology|December 7, 2007
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patientsRudolf A Kley, Yorck Hellenbroich, Peter F M van der Ven, et al.
Nature Communications|September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe diseaseLina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Brain : a Journal of Neurology|January 18, 2021
Bi-allelic truncating mutations in VWA1 cause neuromyopathyMarcus Deschauer, Holger Hengel, Katrin Rupprich, et al.
Elife|November 14, 2023
Human skeletal muscle organoids model fetal myogenesis and sustain uncommitted PAX7 myogenic progenitorsLampros Mavrommatis, Hyun-Woo Jeong, Urs Kindler, et al.
Biochemical and Biophysical Research Communications|August 14, 2018
The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?Christoph S Clemen, Lilli Winter, Karl-Heinz Strucksberg, et al.
Histology and Histopathology|March 13, 2013
Morphological spectrum and clinical features of myopathies with tubular aggregatesFabian Funk, Chantal Ceuterick-de Groote, Jean-Jacques Martin, et al.
Journal of Neurology|March 9, 2023
Periostin as a blood biomarker of muscle cell fibrosis, cardiomyopathy and disease severity in myotonic dystrophy type 1Chi D L Nguyen, Aura Cecilia Jimenez-Moreno, Monika Merker, et al.
Brain : a Journal of Neurology|May 10, 2023
Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defectsAndreas Roos, Peter F M van der Ven, Hadil Alrohaif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2022
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre studyMarianela Schiava, Chiseko Ikenaga, Rocío Nur Villar-Quiles, et al.
Neurology. Genetics|July 18, 2025
Muscle Biopsy Findings in Valosin-Containing Protein Multisystem ProteinopathyMarianela Schiava, Yolande Parkhurst, Matthew Henderson, et al.
Pageof 14