SE-ATLAS

Motor neuron disease Acquired motor neuron disease Genetic motor neuron disease Acetazolamide-responsive myotonia Myotonia permanens Myotonia fluctuans Genetic periodic paralysis Neurogenic scapuloperoneal syndrome, Kaeser type Autosomal dominant proximal spinal muscular atrophy Myasthenia gravis Intellectual disability-developmental delay-contractures syndrome Andersen-Tawil syndrome Macrophagic myofasciitis Poliomyelitis Neuromuscular disease Juvenile primary lateral sclerosis Distal myopathy Infantile-onset X-linked spinal muscular atrophy Potassium-aggravated myotonia Myotonic syndrome Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Periodic paralysis Proximal spinal muscular atrophy Bulbospinal muscular atrophy Muscular tumor Postpoliomyelitis syndrome Rippling muscle disease with myasthenia gravis Monomelic amyotrophy Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Primary lateral sclerosis Idiopathic camptocormia 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 Syndrome d'Isaacs Syndrome de Morvan Sclérose latérale amyotrophique juvénile Maladie du muscle squelettique Dystrophie musculaire Paralysie périodique hypokaliémique Paralysie périodique hyperkaliémique Paramyotonie d'Eulenburg Maladie génétique du muscle squelettique Myopathie inflammatoire idiopathique Maladie acquise du muscle squelettique Hyperthermie maligne de l'anesthésie Maladie de la jonction neuromusculaire Camptodactylie de Tel Hashomer Maladie génétique de la jonction neuromusculaire Syndrome myasthénique de Lambert-Eaton Maladie acquise de la jonction neuromusculaire Myopathies non dystrophiques