Latest papers

Surface electromyography features in manual workers affected by carpal tunnel syndrome.

Clinical Course of Bark Scorpion Envenomation Managed Without Antivenom.

Diagnostic Challenge in Desmin Cardiomyopathy With Transformation of Clinical Phenotypes.

Rab11 rescues synaptic dysfunction and behavioural deficits in a Drosophila model of Huntington's disease.

Rab11 rescues synaptic dysfunction and behavioural deficits in a Drosophila model of Huntington's disease.

Cardiovascular magnetic resonance imaging (CMR) reveals characteristic pattern of myocardial damage in patients with mitochondrial myopathy.

Sex-related differences in the relationship between acceleromyographic adductor pollicis train-of-four ratio and clinical manifestations of residual neuromuscular block: a study in healthy volunteers during near steady-state infusion of mivacurium.

Evaluation of the immediate effects of manual acupuncture on brachial bicep muscle function in healthy individuals and poststroke patients: a study protocol of a parallel-group randomized clinical trial.

Clinical manifestations of acetylcholine receptor antibody positive and negative myasthenia gravis.

[Sialic Acid supplementation therapy for distal myopathy with rimmed vacuoles].

Cell excitability necessary for male mating behavior in Caenorhabditis elegans is coordinated by interactions between big current and ether-a-go-go family K(+) channels.

Cyclic Adenosine Monophosphate Metabolism in Synaptic Growth, Strength, and Precision: Neural and Behavioral Phenotype-Specific Counterbalancing Effects between dnc Phosphodiesterase and rut Adenylyl Cyclase Mutations.

Congenital Myasthenic Syndrome: A Brief Review

Mutation spectrum and phenotypic manifestation in FSHD Greek patients.

[Mechanisms of neuromuscular transmission disorder in rats with alloxan diabetes].

Neurogenic and Myogenic Contributions to Hereditary Motor Neuron Disease.

Common and Less Common Peripheral Nerve Disorders Associated with Diabetes.

Toward deconstructing the phenotype of late-onset Pompe disease.

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.

Neuromuscular manifestations of west nile virus infection.