SE-ATLAS

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