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Matthias Vorgerd

Showing results (11-20 of 140) with videos related to

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Cerebellum (London, England)|July 9, 2016
Unveiling of miRNA Expression Patterns in Purkinje Cells During DevelopmentLukas Pieczora, Lara Stracke, Matthias Vorgerd, et al.
Magma (New York, N.Y.)|November 29, 2019
Diffusion tensor imaging of the human thigh: consideration of DTI-based fiber tracking stop criteriaJohannes Forsting, Robert Rehmann, Martijn Froeling, et al.
Muscle & Nerve|February 10, 2011
Central mechanisms during fatiguing muscle exercise in muscular dystrophy and fibromyalgia syndrome: a study with transcranial magnetic stimulationPeter Schwenkreis, Michael Voigt, Monika Hasenbring, et al.
Journal of Neurology|March 3, 2010
Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathyAnne-Katrin Guettsches, Alma Kuechler, Andreas Gal, et al.
Acta Neuropathologica|July 29, 2008
Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 geneKay W Nolte, Andreas R Janecke, Matthias Vorgerd, et al.
Pain|June 24, 2006
Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related copingOliver Rommel, Rudolf A Kley, Gabriele Dekomien, et al.
AJR. American Journal of Roentgenology|March 24, 2010
MRI in lipid-lowering agent-associated myopathy: a retrospective review of 21 casesSoeren A Peters, Rudolf Kley, Martin Tegenthoff, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
CSF Diagnostics: A Potentially Valuable Tool in Neurodegenerative and Inflammatory Disorders Involving Motor Neurons: A ReviewKarsten Krause, Maximilian Wulf, Paula Sommer, et al.
Journal of Child Neurology|September 25, 2002
Rippling muscle disease in childhoodUlrike Schara, Matthias Vorgerd, Nikola Popovic, et al.
Neuromuscular Disorders : NMD|September 29, 2006
Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1Sabine Hoffjan, Charlotte Thiels, Matthias Vorgerd, et al.
Pageof 14

Showing results (11-20 of 140) with videos related to

Sort By:
Pageof 14
Cerebellum (London, England)|July 9, 2016
Unveiling of miRNA Expression Patterns in Purkinje Cells During DevelopmentLukas Pieczora, Lara Stracke, Matthias Vorgerd, et al.
Magma (New York, N.Y.)|November 29, 2019
Diffusion tensor imaging of the human thigh: consideration of DTI-based fiber tracking stop criteriaJohannes Forsting, Robert Rehmann, Martijn Froeling, et al.
Muscle & Nerve|February 10, 2011
Central mechanisms during fatiguing muscle exercise in muscular dystrophy and fibromyalgia syndrome: a study with transcranial magnetic stimulationPeter Schwenkreis, Michael Voigt, Monika Hasenbring, et al.
Journal of Neurology|March 3, 2010
Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathyAnne-Katrin Guettsches, Alma Kuechler, Andreas Gal, et al.
Acta Neuropathologica|July 29, 2008
Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 geneKay W Nolte, Andreas R Janecke, Matthias Vorgerd, et al.
Pain|June 24, 2006
Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related copingOliver Rommel, Rudolf A Kley, Gabriele Dekomien, et al.
AJR. American Journal of Roentgenology|March 24, 2010
MRI in lipid-lowering agent-associated myopathy: a retrospective review of 21 casesSoeren A Peters, Rudolf Kley, Martin Tegenthoff, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
CSF Diagnostics: A Potentially Valuable Tool in Neurodegenerative and Inflammatory Disorders Involving Motor Neurons: A ReviewKarsten Krause, Maximilian Wulf, Paula Sommer, et al.
Journal of Child Neurology|September 25, 2002
Rippling muscle disease in childhoodUlrike Schara, Matthias Vorgerd, Nikola Popovic, et al.
Neuromuscular Disorders : NMD|September 29, 2006
Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1Sabine Hoffjan, Charlotte Thiels, Matthias Vorgerd, et al.
Pageof 14