SE-ATLAS

Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Madras motor neuron disease Amyotrophic lateral sclerosis type 4 Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Morvan syndrome Juvenile amyotrophic lateral sclerosis Skeletal muscle disease Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Genetic skeletal muscle disease Muscular dystrophy Paramyotonia congenita of Von Eulenburg Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy Acquired neuromuscular junction disease Lambert-Eaton myasthenic syndrome Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Autosomal dominant proximal spinal muscular atrophy Neurogenic scapuloperoneal syndrome, Kaeser type Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Congenital myasthenic syndrome Genetic periodic paralysis Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Myotonic syndrome Potassium-aggravated myotonia Periodic paralysis Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Bulbospinal muscular atrophy Proximal spinal muscular atrophy Rippling muscle disease with myasthenia gravis Postpoliomyelitis syndrome Muskeltumor Myopathie bei infektiösen und parasitären Krankheiten Amyotrophie, monomelische Fazio-neuro-muskulo-skelettales Syndrom, zyprischer Typ