SE-ATLAS

Cerebral sinovenous thrombosis Progressive encephalomyelitis with rigidity and myoclonus Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy Trigeminal neuralgia Idiopathic intracranial hypertension Amyotrophic lateral sclerosis Glycogen storage disease due to acid maltase deficiency Hereditary ATTR amyloidosis Multiple system atrophy, parkinsonian type Glial tumor SUNCT syndrome Hereditary neuropathy with liability to pressure palsies Multifocal motor neuropathy Lambert-Eaton myasthenic syndrome Leukodystrophy Limb-girdle muscular dystrophy Rare dystonia Herpes simplex virus encephalitis Calpain-3-related limb-girdle muscular dystrophy R1 Acute disseminated encephalomyelitis Facioscapulohumeral dystrophy Blepharospasm-oromandibular dystonia syndrome Giant cell arteritis Moyamoya disease Huntington disease Steinert myotonic dystrophy Mitochondrial DNA-related progressive external ophthalmoplegia Focal stiff limb syndrome Lyme disease CLIPPERS Autosomal recessive progressive external ophthalmoplegia MELAS Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy NMDA receptor encephalitis Muscular dystrophy Hypokalemic periodic paralysis Hyperkalemic periodic paralysis Neuromyelitis optica spectrum disorder Progressive supranuclear palsy Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Marfan syndrome Autosomal dominant progressive external ophthalmoplegia Progressive muscular atrophy Multiple system atrophy, cerebellar type Limbic encephalitis Limbic encephalitis with caspr2 antibodies Guillain-Barré syndrome Tuberculous meningitis Classic stiff person syndrome Meningioma Primary angiitis of the central nervous system Meningococcal meningitis Persistent idiopathic facial pain Limbic encephalitis with LGI1 antibodies Susac syndrome Fragile X-associated tremor/ataxia syndrome Sporadic Creutzfeldt-Jakob disease Myasthenia gravis Becker muscular dystrophy Myofibrillar myopathy Duchenne muscular dystrophy FKRP-related limb-girdle muscular dystrophy R9 Neuralgic amyotrophy Familial Mediterranean fever Anoctamin-5-related limb-girdle muscular dystrophy R12 Distal myopathy Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Dermatomyositis Proximal myotonic myopathy Autosomal recessive axonal neuropathy with neuromyotonia Reversible cerebral vasoconstriction syndrome Kennedy disease Corticobasal syndrome Late-onset distal myopathy, Markesbery-Griggs type Autosomal dominant cerebellar ataxia Inclusion body myositis Thomsen and Becker disease Glioblastoma Leber hereditary optic neuropathy Primary lateral sclerosis Immune-mediated necrotizing myopathy Chronic inflammatory demyelinating polyneuropathy Behçet disease Hereditary hyperekplexia Isolated dystonia Autosomal recessive limb-girdle muscular dystrophy Stiff person spectrum disorder Dystonie dopa-sensible