SE-ATLAS

Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy Eosinophilic fasciitis Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Inflammatory myopathy with abundant macrophages Idiopathic eosinophilic myositis Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Genetic periodic paralysis Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Neuromuscular disease Poliomyelitis Polymyositis Distal myopathy Juvenile primary lateral sclerosis Infantile-onset X-linked spinal muscular atrophy Infantile-onset ascending hereditary spastic paralysis Inclusion body myositis Bulbospinal muscular atrophy Potassium-aggravated myotonia Myotonic syndrome Thomsen and Becker disease Immune-mediated necrotizing myopathy Proximal spinal muscular atrophy Periodic paralysis Muscular tumor Overlap myositis Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Monomelic amyotrophy Antisynthetase syndrome Cyprus facial-neuromusculoskeletal syndrome Dermatomyositis Infectious, fungal or parasitic myopathy Focal myositis Primary lateral sclerosis Idiopathic camptocormia Juvenile idiopathic inflammatory myopathy Muscular dystrophy-white matter spongiosis syndrome Amyotrophic lateral sclerosis type 4 Madras motor neuron disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Skeletal muscle disease Hypokalemic periodic paralysis Muscular dystrophy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Genetic skeletal muscle disease Idiopathic inflammatory myopathy Acquired skeletal muscle disease