SE-ATLAS

Morvan syndrome Skeletal muscle disease Hypokalemic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis 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 fluctuans Acquired motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Andersen-Tawil syndrome Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Infantile-onset X-linked spinal muscular atrophy Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Bulbospinal muscular atrophy Proximal spinal muscular atrophy Postpoliomyelitis syndrome Monomelic amyotrophy Primary lateral sclerosis Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Muscular channelopathy Amyotrophic lateral sclerosis Isaacs syndrome