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Clemen, Christoph S., Tangavelou, Karthikeyan, Strucksberg, Karl-Heinz, Just, Steffen, Gaertner, Linda, Regus-Leidig, Hanna, Stumpf, Maria, Reimann, Jens, Coras, Roland, Morgan, Reginald O. ORCID: 0000-0002-2059-792X, Fernandez, Maria-Pilar, Hofmann, Andreas
ORCID: 0000-0003-4408-5467, Mueller, Stefan, Schoser, Benedikt
ORCID: 0000-0002-2757-8131, Hanisch, Franz-Georg, Rottbauer, Wolfgang, Bluemcke, Ingmar, von Hoersten, Stephan, Eichinger, Ludwig
ORCID: 0000-0003-1594-6117 and Schroeder, Rolf
(2010).
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.
Brain, 133.
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OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2156
Feldkirchner, Sarah, Schessl, Joachim, Mueller, Stefan, Schoser, Benedikt ORCID: 0000-0002-2757-8131 and Hanisch, Franz-Georg
(2012).
Patient-specific protein aggregates in myofibrillar myopathies: Laser microdissection and differential proteomics for identification of plaque components.
Proteomics, 12 (23-24).
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HOBOKEN:
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ISSN 1615-9853
Lehmann, Helmar C., Schoser, Benedikt, Wunderlich, Gilbert, Berlit, Peter and Fink, Gereon R. ORCID: 0000-0002-8230-1856
(2021).
Neuromuscular complications of SARS-CoV-2 infection-Part 2: muscle disorders.
Nervenarzt, 92 (6).
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NEW YORK:
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ISSN 1433-0407
Lehmann, Helmar C., Schoser, Benedikt, Wunderlich, Gilbert, Berlit, Peter and Fink, Gereon R. ORCID: 0000-0002-8230-1856
(2021).
Neuromuscular complications of SARS-CoV-2 infections-Part 1: peripheral nerves.
Nervenarzt, 92 (6).
S. 540 - 548.
NEW YORK:
SPRINGER.
ISSN 1433-0407
Mengel, David, Librizzi, Damiano, Schoser, Benedikt, Glaeser, Dieter, Clemen, Christoph S., Dodel, Richard and Schroeder, Rolf (2018). Inclusion Body Myopathy, Paget's Disease, and Fronto-temporal Dementia: a VCP-related Multi-systemic Proteinopathy. Forschritte Neurol. Psychiatr., 86 (7). S. 434 - 439. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3522
Schessl, Joachim, Bach, Elisa, Rost, Simone, Feldkirchner, Sarah, Kubny, Christiana, Mueller, Stefan, Hanisch, Franz-Georg, Kress, Wolfram and Schoser, Benedikt ORCID: 0000-0002-2757-8131
(2014).
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
Neurogenetics, 15 (3).
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NEW YORK:
SPRINGER.
ISSN 1364-6753