Neuromuscular Disorders

Titel Veröffentlichungsdatum Sprache Zitate
Retrospective Analysis of Efgartigimod Use in Patients with Double-seronegative Generalized Myasthenia Gravis: A Case Series2024/04/01English
Editorial Board2024/04/01English
WMS 2024 Congress Flyer2024/04/01English
WMS General Information2024/04/01English
Update in Neuromuscular Disorder Course announcement2024/04/01English
WMS 2024 Congress information2024/04/01English
28th ENMC international workshop: Mitochondrial diseases1995/07/01English
A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNA2001/07/01English
Erratum to “Axon damage in CMT due to mutation in myelin protein P0” [Neuromusc. Disord. 11 (2001) 753–756]2002/05/01English
Expression of laminin subunits in congenital muscular dystrophy1995/07/01English
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: A possible sequel of drug toxicity in first trimester of pregnancy?1995/01/01English
Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient2000/03/01English
Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes2001/07/01English
High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy2000/06/01English
Instructions to authors2001/07/01English
WMS Information2023/09/01English
Editorial Board2023/09/01English
WMS 2023 Flyer2023/09/01English
WMS 2023 Congress announcement2023/09/01English
Introducing the Dysphagiameter: a novel patient-reported outcome measure for evaluating dysphagia in oculopharyngeal muscular dystrophy - from conceptual framework to initial development2023/11/01English
WMS Information2023/07/01English
WMS 2023 Flyer2023/07/01English
WMS 2023 Congress announcement2023/07/01English
Muscle magnetic resonance imaging of a large cohort of distal hereditary motor neuropathies reveals characteristic features useful for diagnosis2023/10/01English
An early onset benign myopathy with glycogen storage caused by a de novo 1.4 Mb-deletion of chromosome 142023/10/01English
Suitability of the Respicheck questionnaire and Epworth sleepiness scale for therapy monitoring in myotonic dystrophy type 12023/10/01English
WMS 2023 Congress announcement2023/08/01English
WMS Information2023/08/01English
WMS 2023 Flyer2023/08/01English
Editorial Board2023/08/01English