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Neuropediatrics|July 4, 2007
Clinical presentation and course of childhood Guillain-Barré syndrome: a prospective multicentre studyR Korinthenberg, J Schessl, J Kirschner
Neuromuscular Disorders : NMD|December 3, 2014
Muscle ultrasound in classic infantile and adult Pompe disease: a useful screening tool in adults but not in infantsK Vill, J Schessl, V Teusch, et al.
Neuropediatrics|June 24, 2010
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1J Schessl, A Columbus, Y Hu, et al.
Archives of Disease in Childhood|August 22, 2006
Prospective study on anti-ganglioside antibodies in childhood Guillain-Barré syndromeJ Schessl, M Koga, K Funakoshi, et al.
Neuromuscular Disorders : NMD|May 9, 2018
A zebrafish model for FHL1-opathy reveals loss-of-function effects of human FHL1 mutationsM Keßler, A Kieltsch, E Kayvanpour, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 15, 2009
Phenotypic variability in siblings with calpainopathy (LGMD2A)J Schessl, M C Walter, G Schreiber, et al.
Neuromuscular Disorders : NMD|July 21, 2009
Muscle MRI in FHL1-linked reducing body myopathyG Astrea, J Schessl, E Clement, et al.
Neuropediatrics|May 6, 2004
Low level of intracortical inhibition in children shown by transcranial magnetic stimulationV Mall, S Berweck, U M Fietzek, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
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