S. Feldkirchner

Patient‐specific protein aggregates in myofibrillar myopathies: Laser microdissection and differential proteomics for identification of plaque components

J. Schessl, B. Schoser, S. Müller, 2012, Proteomics.

Novel recessive myotilin mutation causes severe myofibrillar myopathy

J. Schessl, W. Kress, B. Schoser, 2014, neurogenetics.

Reducing body myopathy and other FHL1-related muscular disorders.

J. Schessl, B. Schoser, S. Feldkirchner, 2011, Seminars in pediatric neurology.

New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses

M. Tegenthoff, M. Vorgerd, M. Eisenacher, 2016, Acta neuropathologica communications.

Novel recessive myotilin mutation causes severe myofibrillar myopathy

J. Schessl, W. Kress, B. Schoser, 2014, neurogenetics.

Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy

J. Schessl, W. Kress, B. Schoser, 2013, Neuromuscular Disorders.