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The nature of respiratory muscle weakness in patients with late-onset-Pompe disease

Chronic inflammatory demyelinating polyneuropathy: Plasmapheresis or cyclosporine can be good treatment options in refractory cases

X-linked Emery-Dreifuss muscle dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures

Muscle biopsies in clinical trials for Duchenne muscular dystrophy – patients’ and caregivers’ perspective

Clinical spectrum and gene mutations in a Chinese cohort with Anoctaminopathy

European regulators’ views on a wearable-derived performance measurement of Ambulation for Duchenne Muscular Dystrophy regulatory trials

The prevalence of faecal incontinence in myotonic dystrophy type 1

Evolution of bone mineral density, bone metabolism and fragility fractures in Spinal Muscular Atrophy (SMA) types 2 and 3.

Stopping Oral Steroid-Sparing Agents at Initiation of Rituximab in Myasthenia Gravis

Spinal Muscular Atrophy Revisited

Critical Review Ahead of Publication

The World Wide Web (WWW): For better or for worse

Editorial Board

Severe distal muscle involvement and mild sensory neuropathy in a boy with infantile onset Pompe disease treated with enzyme replacement therapy for 6 years

1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018

Muscle fiber dysfunction contributes to weakness in inclusion body myositis

Recessive MYH7-related myopathy in two families

A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement

Central drive and ventilatory failure in late-onset Pompe disease: At the gates of a new phenotype

Polyradiculoneuropathy in dourine-affected horses

Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease

PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability

Thoracic circumference: A new outcome measure in spinal muscular atrophy type 1?

Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates

Concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase antibody with reducing body myopathy: Possible double trouble

Longitudinal Study of Upper Extremity Reachable Workspace in Fascioscapulohumeral Muscular Dystrophy

Efficient gene transfer into primary muscle cells to analyse nerve-independent postsynaptic organization in vitro

Inflammation-induced fibrosis in skeletal muscle of female carriers of Duchenne muscular dystrophy

Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene

Rhabdomyolysis and myoglobinuria following bisphosphonate infusion in patients with Duchenne muscular dystrophy

Autosomal recessive axonal neuropathy caused by HINT1 mutation: new association of a psychiatric disorder to the neurologic phenotype

Unraveling upper extremity performance in Duchenne muscular dystrophy: A biophysical model

Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia

Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement

Newborn screening for SMA in Southern Belgium

Editorial Board

237th ENMC International Workshop: GNE myopathy – current and future research Hoofddorp, The Netherlands, 14–16 September 2018

Wrist drop in an arcade dancing game: Unusual sudden bilateral radial palsy

Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian family

ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles

A review of the histopathological findings in myasthenia gravis: Clues to the pathogenesis of treatment-resistance in extraocular muscles

Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRI

Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II

Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling

The relations of parental supervision, parental school involvement, and child's social competence with school achievement in primary school

A Study on the Application and Use of Artificial Intelligence to Support Drug Development

A Simulated Application of the Hartford Hospital Aminoglycoside Dosing Nomogram for Plazomicin Dosing Interval Selection in Patients With Serious Infections Caused by Carbapenem-Resistant Enterobacterales

Efficacy and Safety of Udenafil for the Treatment of Pulmonary Arterial Hypertension: a Placebo-controlled, Double-blind, Phase IIb Clinical Trial

Comparative Bioavailability Study of a New Orodispersible Formulation of Ibuprofen Versus Two Existing Oral Tablet Formulations in Healthy Male and Female Volunteers

Regulatory Considerations on the Development, Evaluation, and Approval of Therapies in Rheumatoid Arthritis Prevention