SE-ATLAS

Cerebral sinovenous thrombosis Hereditary hyperekplexia Calpain-3-related limb-girdle muscular dystrophy R1 Limbic encephalitis with LGI1 antibodies Classic stiff person syndrome Focal stiff limb syndrome Progressive encephalomyelitis with rigidity and myoclonus Marfan syndrome Hereditary neuropathy with liability to pressure palsies Multifocal motor neuropathy Acute disseminated encephalomyelitis Mitochondrial DNA-related progressive external ophthalmoplegia Hyperkalemic periodic paralysis Progressive supranuclear palsy Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Multiple system atrophy, cerebellar type Leukodystrophy Limb-girdle muscular dystrophy Rare dystonia Facioscapulohumeral dystrophy Blepharospasm-oromandibular dystonia syndrome Steinert myotonic dystrophy Glial tumor SUNCT syndrome Tuberculous meningitis Fabry disease Lambert-Eaton myasthenic syndrome Huntington disease Autosomal dominant progressive external ophthalmoplegia Limbic encephalitis with caspr2 antibodies Meningioma Moyamoya disease Idiopathic intracranial hypertension MELAS Neuromyelitis optica spectrum disorder Progressive muscular atrophy Limbic encephalitis Guillain-Barré syndrome Fragile X-associated tremor/ataxia syndrome Myasthenia gravis Becker muscular dystrophy Myofibrillar myopathy 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 Maligne Hyperthermie Spinale Muskelatrophie, proximale, Typ 3 Spinale Muskelatrophie, proximale, Typ 2 Kennedy-Krankheit ATTR-Amyloidose, hereditäre Dystonie, isolierte