SE-ATLAS

Progressive myoclonic epilepsy Adolescent-onset epilepsy syndrome Epilepsy syndrome Transient neonatal myasthenia gravis Neurocutaneous syndrome with epilepsy Benign adult familial myoclonic epilepsy Familial temporal lobe epilepsy Chromosomal anomaly with epilepsy as a major feature Familial focal epilepsy with variable foci Hereditary ataxia Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Monogenic disease with epilepsy New-onset refractory status epilepticus Inflammatory and autoimmune disease with epilepsy Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Rare headache Lambert-Eaton myasthenic syndrome Proximal spinal muscular atrophy Congenital myasthenic syndrome Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome Hypnic headache PEHO-like syndrome Generalized epilepsy with febrile seizures-plus PEHO syndrome Rare epilepsy Autosomal dominant epilepsy with auditory features Moynahan syndrome Rare ataxia Muscular channelopathy Skeletal muscle disease SUNCT syndrome Acquired peripheral neuropathy Reversible cerebral vasoconstriction syndrome Oculocerebrocutaneous syndrome Neuromuscular junction disease Cranial neuralgia Nervenkrankheit, periphere, genetisch bedingte Nervenkrankheit, periphere Migräne, hemiplegische, familiäre oder sporadische Form Aktionsmyoklonus-Nierenversagen-Syndrom DEND-Syndrom Hemikranie, paroxysmale Motoneuronkrankheit Charcot-Marie-Tooth-Krankheit/Hereditäre motorische und sensorische Neuropathie Generalisierte Epilepsie-paroxysmale Dyskinesie-Syndrom Absencen-Epilepsie, juvenile Ganglionopathie, erworbene sensorische Epilepsie, familiäre partielle Neuralgische Amyotrophie Reflexepilepsie, genetisch-bedingte Nächtliche Frontallappenepilepsie, autosomal-dominante Absencen-Epilepsie des Kindesalters Benigne familiäre Neugeborenenepilepsie Trigeminoautonome Kopfschmerzen Myasthenia gravis Benigne fokale Adoleszenten-Epilepsie Myasthenia gravis mit Beginn im Erwachsenenalter Temporallappenepilepsie, mesiale, familiäre Form Neuromuskuläre Krankheit Juvenile Myasthenia gravis Chronische inflammatorische demyelinisierende Polyneuropathie