SE-ATLAS

Guillain-Barré syndrome Transient neonatal myasthenia gravis Infantile-onset ascending hereditary spastic paralysis Bulbospinal muscular atrophy Potassium-aggravated myotonia Thomsen and Becker disease Proximal spinal muscular atrophy Postpoliomyelitis syndrome Monomelic amyotrophy Primary lateral sclerosis Amyotrophic lateral sclerosis type 4 Juvenile dermatomyositis Progressive muscular atrophy Madras motor neuron disease Sarcoidosis Behçet disease Scapuloperoneal spinal muscular atrophy Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Distal hereditary motor neuropathy Paramyotonia congenita of Von Eulenburg Acquired skeletal muscle disease Genetic skeletal muscle disease Neuromuscular junction disease Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Motor neuron disease Genetic motor neuron disease Periodic paralysis with transient compartment-like syndrome Acquired motor neuron disease Neurogenic scapuloperoneal syndrome, Kaeser type Adult-onset myasthenia gravis Whipple disease Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Andersen-Tawil syndrome Poliomyelitis Juvenile myasthenia gravis Neuromuscular disease Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Juvenile amyotrophic lateral sclerosis