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Neuromuscular Disorders : NMD|December 30, 2020
A novel mutation in NEB causing foetal nemaline myopathy with arthrogryposis during early gestationMaria L Rocha, Carsten Dittmayer, Akinori Uruha, et al.
Neuromuscular Disorders : NMD|February 14, 2024
"Amyopathic" MDA5-positive dermatomyositis with severe lung involvement presenting with net myositic morphological features - insights from an autopsy studyBenjamin Englert, Carsten Dittmayer, Hans-Hilmar Goebel, et al.
Brain Pathology (Zurich, Switzerland)|May 27, 2021
Inflammatory features in sporadic late-onset nemaline myopathy are independent from monoclonal gammopathyJantima Tanboon, Akinori Uruha, Yukie Arahata, et al.
Neuromuscular Disorders : NMD|January 3, 2026
Monoclonal Gammopathy - the common denominator of sporadic late-onset nemaline myopathy and paraproteinemic neuropathyEleonora Torchia, Frauke Stascheit, Felix Kleefeld, et al.
Seminars in Pediatric Neurology|July 3, 2018
The Curse of Apneic SpellsJosefine Radke, Mona Dreesmann, Michael Radke, et al.
Cells|January 11, 2022
Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile PatientsAnne Schänzer, Leonie Rager, Iris Dahlhaus, et al.
Neuromuscular Disorders : NMD|August 29, 2018
New variant of necklace fibres display peculiar lysosomal structures and mitophagyJan Leo Rinnenthal, Carsten Dittmayer, Kerstin Irlbacher, et al.
The American Journal of Pathology|October 13, 2012
Immune-mediated necrotizing myopathy is characterized by a specific Th1-M1 polarized immune profileCorinna Preuße, Hans H Goebel, Josephin Held, et al.
Annals of Clinical and Translational Neurology|November 28, 2018
Autophagic vacuolar myopathy is a common feature of CLN3 diseaseJosefine Radke, Randi Koll, Esther Gill, 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.
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