SE-ATLAS

Zerebrale Sinus- und Venenthrombose Hyperekplexie, hereditäre Calpain-3-assoziierte Gliedergürtelmuskeldystrophie R1 Limbische Enzephalitis mit LGI1-Antikörpern Stiff-person-Syndrom, klassisches Fokales Stiff-Limb-Syndrom Progressive Enzephalomyelitis mit Rigidität und Myoklonus Marfan-Syndrom Hereditäre Neuropathie mit Neigung zu Drucklähmungen Multifokale motorische Neuropathie Enzephalomyelitis, akute disseminierte Ophthalmoplegie, chronische externe progressive, maternal-vererbte Paralyse, hyperkaliämische periodische Progressive supranukleäre Blickparese Paramyotonia congenita Eulenburg Hereditäre spastische Paraplegie Multisystematrophie, zerebellärer Typ Leukodystrophie Gliedergürtelmuskeldystrophie Dystonie Muskeldystrophie, fazio-skapulo-humerale Blepharospasmus-oromandibuläre Dystonie-Syndrom Myotone Dystrophie Steinert Gliom SUNCT-Syndrom Meningitis, tuberkulöse Fabry-Syndrom Lambert-Eaton-Myasthenie-Syndrom Huntington-Krankheit Ophthalmoplegie, externe progressive, autosomal-dominante Limbische Enzephalitis mit Caspr2-Antikörper Meningeom Moyamoya-Krankheit Hypertension, idiopathische intrakranielle MELAS Neuromyelitis-optica-Spektrum-Störung Progressive Muskelatrophie Limbische Enzephalitis Guillain-Barré-Syndrom Fragiles-X assoziiertes Tremor/Ataxie-Syndrom Myasthenia gravis Muskeldystrophie Typ Becker Myopathie, myofibrilläre Duchenne muscular dystrophy Distal myopathy Proximal myotonic myopathy Late-onset distal myopathy, Markesbery-Griggs type Inclusion body myositis Autosomal dominant cerebellar ataxia Thomsen and Becker disease Leber hereditary optic neuropathy Multiple system atrophy, parkinsonian type Behçet disease Stiff person spectrum disorder Autosomal recessive limb-girdle muscular dystrophy Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy NMDA receptor encephalitis Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Muscular dystrophy Hypokalemic periodic paralysis Primary angiitis of the central nervous system Meningococcal meningitis Sporadic Creutzfeldt-Jakob disease FKRP-related limb-girdle muscular dystrophy R9 Anoctamin-5-related limb-girdle muscular dystrophy R12 Dermatomyositis Reversible cerebral vasoconstriction syndrome Corticobasal syndrome Immune-mediated necrotizing myopathy Dopa-responsive dystonia Amyotrophic lateral sclerosis CLIPPERS Persistent idiopathic facial pain Susac syndrome Neuralgic amyotrophy Familial Mediterranean fever Autosomal recessive axonal neuropathy with neuromyotonia Glioblastoma Primary lateral sclerosis Glycogen storage disease due to acid maltase deficiency Chronic inflammatory demyelinating polyneuropathy Wilson disease Herpes simplex virus encephalitis Giant cell arteritis Lyme disease Trigeminal neuralgia Autosomal recessive progressive external ophthalmoplegia Malignant hyperthermia of anesthesia Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Kennedy disease Hereditary ATTR amyloidosis Isolated dystonia