SE-ATLAS

Amyotrophic lateral sclerosis type 4 Muscular dystrophy-white matter spongiosis syndrome Madras motor neuron disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Skeletal muscle disease Genetic skeletal muscle disease Hypokalemic periodic paralysis Muscular dystrophy Hyperkalemic periodic paralysis Juvenile amyotrophic lateral sclerosis Acquired skeletal muscle disease Paramyotonia congenita of Von Eulenburg Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Non-dystrophic myopathy Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Genetic periodic paralysis Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy 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 Monomelic amyotrophy Infectious, fungal or parasitic myopathy Rippling muscle disease with myasthenia gravis Cyprus facial-neuromusculoskeletal syndrome Primary lateral sclerosis Idiopathic camptocormia