SE-ATLAS

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