SE-ATLAS

Myopathies non dystrophiques Maladie génétique de la jonction neuromusculaire Maladie acquise de la jonction neuromusculaire Maladie du motoneurone Myotonie fluctuante Maladie acquise du motoneurone Maladie génétique du motoneurone Myotonie sensible à l'acétazolamide Myotonie permanente Amyotrophie spinale proximale autosomique dominante Syndrome scapulo-péronier neurogénique type Kaeser Paralysie périodique génétique Myasthénie auto-immune Syndrome de déficience intellectuelle-retard de développement-contractures Paralysie périodique avec pseudo-syndrome des loges transitoire Andersen-Tawil syndrome Macrophagic myofasciitis Neuromuscular disease Distal myopathy Infantile-onset X-linked spinal muscular atrophy Juvenile primary lateral sclerosis Myotonic syndrome Potassium-aggravated myotonia Infantile-onset ascending hereditary spastic paralysis Thomsen and Becker disease Bulbospinal muscular atrophy Proximal spinal muscular atrophy Periodic paralysis Muscular tumor Infectious, fungal or parasitic myopathy Cyprus facial-neuromusculoskeletal syndrome Primary lateral sclerosis Idiopathic camptocormia Muscular dystrophy-white matter spongiosis syndrome Madras motor neuron disease Idiopathic dropped head syndrome Amyotrophic lateral sclerosis type 4 Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Progressive muscular atrophy Amyotrophic lateral sclerosis Muscular channelopathy Isaacs syndrome Scapuloperoneal spinal muscular atrophy Juvenile amyotrophic lateral sclerosis Morvan syndrome Skeletal muscle disease Genetic skeletal muscle disease Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Distal hereditary motor neuropathy Acquired skeletal muscle disease Idiopathic inflammatory myopathy Malignant hyperthermia of anesthesia Neuromuscular junction disease Tel Hashomer camptodactyly syndrome