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Acta Neurologica Scandinavica|February 27, 2016
Secondary myopathy due to systemic diseasesJ Finsterer, W N Löscher, J Wanschitz, et al.Acta Neurologica Scandinavica|March 16, 2017
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's diseaseJ Finsterer, J Wanschitz, S Quasthoff, et al.Acta Neurologica Scandinavica|April 18, 2015
Iatrogenic lesions of peripheral nervesW N Löscher, J Wanschitz, S Iglseder, et al.Journal of the Neurological Sciences|July 18, 2016
Neuromuscular complications in cancerW Grisold, A Grisold, W N LöscherEuropean Neurology|August 31, 2001
Nail-patella syndrome associated with respiratory chain disorderJ Finsterer, C Stöllberger, J Wanschitz, et al.Muscle & Nerve|May 22, 2001
Acquired neuromyotonia and peripheral neuropathy in a patient with Hodgkin's diseaseH Lahrmann, G Albrecht, M Drlicek, et al.Journal of the Neurological Sciences|April 15, 1997
Light chain myeloma with oro-pharyngeal amyloidosis presenting as bulbar paralysisJ Finsterer, C Wogritsch, P Pokieser, et al.Muscle & Nerve|September 15, 1998
The role of axonal ion conductances in diabetic neuropathy: a reviewS QuasthoffNeuroscience Letters|March 14, 1994
A mechanosensitive K+ channel with fast-gating kinetics on human axons blocked by gadolinium ionsS QuasthoffEuropean Journal of Applied Physiology and Occupational Physiology|January 1, 1993
Myo-electric signals from two extrinsic hand muscles and force tremor during isometric handgripW N Löscher, E GallaschPageof 37