SE-ATLAS

Juvenile amyotrophic lateral sclerosis Morvan syndrome Muscular dystrophy Skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Hypokalemic periodic paralysis Genetic skeletal muscle disease Hyperkalemic periodic paralysis Distal hereditary motor neuropathy Paramyotonia congenita of Von Eulenburg Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Non-dystrophic myopathy Genetic neuromuscular junction disease Genetic motor neuron disease 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 Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Periodic paralysis with transient compartment-like syndrome Genetic periodic paralysis Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Myotonic syndrome Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Periodic paralysis Thomsen and Becker disease Bulbospinal muscular atrophy Proximal spinal muscular atrophy Postpoliomyelitis syndrome Muscular tumor Monomelic amyotrophy Infectious, fungal or parasitic myopathy Cyprus facial-neuromusculoskeletal syndrome Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Idiopathic dropped head syndrome Scapuloperoneal spinal muscular atrophy Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Muscular channelopathy Amyotrophic lateral sclerosis Progressive muscular atrophy Isaacs syndrome