SE-ATLAS

Amyotrophic lateral sclerosis Muscular channelopathy Scapuloperoneal spinal muscular atrophy Isaacs syndrome Juvenile amyotrophic lateral sclerosis Morvan syndrome Skeletal muscle disease Hypokalemic periodic paralysis Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Distal hereditary motor neuropathy Hyperkalemic periodic paralysis Genetic skeletal muscle disease Paramyotonia congenita of Von Eulenburg Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Genetic neuromuscular junction disease Motor neuron disease Genetic motor neuron disease Myotonia permanens Myotonia fluctuans Acquired motor neuron disease Acetazolamide-responsive myotonia Periodic paralysis with transient compartment-like syndrome Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Andersen-Tawil syndrome Neuromuscular disease Juvenile primary lateral sclerosis Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Potassium-aggravated myotonia Thomsen and Becker disease Proximal spinal muscular atrophy Bulbospinal muscular atrophy Primary lateral sclerosis Amyotrophic lateral sclerosis type 4 Madras motor neuron disease Progressive muscular atrophy