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Number of items: 4.

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. S. 2920 - 2942. 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). S. 3598 - 3610. HOBOKEN: WILEY-BLACKWELL. ISSN 1615-9853

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). S. 151 - 157. NEW YORK: SPRINGER. ISSN 1364-6753

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