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 Motoneuronkrankheit, erworbene Vogt-Koyanagi-Harada-Krankheit Fokales Stiff-Limb-Syndrom Periodische Paralyse mit transienten Kompartment-ähnlichem Syndrom Hyperekplexie, hereditäre Stiff-person-Syndrom, klassisches Trigeminoautonome Kopfschmerzen Andersen-Tawil-Syndrom Neuromuskuläre Krankheit Guillain-Barré-Syndrom Stiff-person-Spektrum-Erkrankungen Myotonie, Kalium-sensitive CLIPPERS Chronische inflammatorische demyelinisierende Polyneuropathie Myotonia congenita Typ Thomsen und Becker Hemicrania continua CANOMAD-Syndrom Lateralsklerose, primäre Polyneuropathie mit monoklonaler IgM-Gammopathie mit Anti-MAG Kopfschmerz, seltene Form Kopfschmerz, schlafgebundener Multiple Sklerose variante Progressive Enzephalomyelitis mit Rigidität und Myoklonus