SE-ATLAS

Schilder disease Rare epilepsy Marburg acute multiple sclerosis Rare neuroinflammatory or neuroimmunological disease Progressive muscular atrophy Muscular channelopathy Amyotrophic lateral sclerosis Brain inflammatory disease Baló concentric sclerosis Isaacs syndrome Acute disseminated encephalomyelitis Morvan syndrome SUNCT syndrome Skeletal muscle disease Genetic skeletal muscle disease Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromyelitis optica spectrum disorder Neuromuscular junction disease Acquired neuromuscular junction disease Genetic motor neuron disease Paroxysmal hemicrania Paraneoplastic neurologic syndrome Familial or sporadic hemiplegic migraine Hypokalemic periodic paralysis Genetic neuromuscular junction disease Motor neuron disease Acquired motor neuron disease Vogt-Koyanagi-Harada disease Focal stiff limb syndrome Periodic paralysis with transient compartment-like syndrome Hereditary hyperekplexia Classic stiff person syndrome Trigeminal autonomic cephalalgia Andersen-Tawil syndrome Neuromuscular disease Guillain-Barré syndrome Stiff person spectrum disorder Myotonie aggravée par le potassium CLIPPERS Polyradiculonévrite inflammatoire démyélinisante chronique Myotonie congénitale de Thomsen et Becker Hémicrânie continue Syndrome CANOMAD Sclérose latérale primitive Polyneuropathie associée à une gammopathie monoclonale IgM ayant une activité anti-MAG Céphalée rare Céphalée hypnique Variant de la sclérose en plaques Encéphalomyélite progressive avec rigidité et myoclonies