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Journal of Neuromuscular Diseases|August 4, 2020
Familial Oculo-Leptomeningeal Transthyretin Amyloidosis Caused by Leu55Arg MutationFelix Kleefeld, Fabian Knebel, Dennis Eurich, et al.
Der Nervenarzt|October 1, 2020
[Neurological complications of hepatitis C infections]Felix Kleefeld, Gabriele Arendt, Eva Neuen-Jacob, et al.
Neuromuscular Disorders : NMD|February 6, 2026
Spontaneous remission in statin-associated HMGCR-positive immune-mediated necrotizing myopathy after statin withdrawalAgata A Mossakowski, Daniel Pascale, Yves Allenbach, et al.
ESC Heart Failure|October 4, 2020
Isolated atrial amyloidosis suspected by electrophysiological voltage mapping and diagnosed by <sup>99m</sup> Tc-DPD scintigraphyDoreen Schöppenthau, Imke Schatka, Alexander Berger, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|January 7, 2022
Same same, but different? The neurological presentation of wildtype transthyretin (ATTRwt) amyloidosisFelix Kleefeld, Elise Scherret, Fabian Knebel, et al.
Neurology|October 4, 2022
Morphologic and Molecular Patterns of Polymyositis With Mitochondrial Pathology and Inclusion Body MyositisFelix Kleefeld, Akinori Uruha, Anne Schänzer, et al.
Acta Neuropathologica|January 12, 2024
Complement and MHC patterns can provide the diagnostic framework for inflammatory neuromuscular diseasesChristopher Nelke, Simone Schmid, Felix Kleefeld, et al.
Neuropathology and Applied Neurobiology|May 10, 2021
Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reasonFelix Kleefeld, Anja von Renesse, Carsten Dittmayer, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 1, 2026
Longitudinal Assessment of Muscle Involvement in Late-Onset Pompe Disease Using Quantitative MRI: A Prospective Cohort StudyAlice De Lorenzo, Johannes Forsting, Martijn Froeling, et al.
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