SE-ATLAS

Cerebral sinovenous thrombosis Calpain-3-related limb-girdle muscular dystrophy R1 Hereditary hyperekplexia Focal stiff limb syndrome Classic stiff person syndrome Limbic encephalitis with LGI1 antibodies Progressive encephalomyelitis with rigidity and myoclonus Hereditary neuropathy with liability to pressure palsies Multifocal motor neuropathy Lambert-Eaton myasthenic syndrome Leukodystrophy Limb-girdle muscular dystrophy Rare dystonia Acute disseminated encephalomyelitis Facioscapulohumeral dystrophy Blepharospasm-oromandibular dystonia syndrome Huntington disease Steinert myotonic dystrophy Mitochondrial DNA-related progressive external ophthalmoplegia Hyperkalemic periodic paralysis Progressive supranuclear palsy Paramyotonia congenita of Von Eulenburg Hereditary spastic paraplegia Marfan syndrome Autosomal dominant progressive external ophthalmoplegia Glial tumor Multiple system atrophy, cerebellar type SUNCT syndrome Tuberculous meningitis Herpes simplex virus encephalitis Moyamoya disease Giant cell arteritis Lyme disease CLIPPERS Autosomal recessive progressive external ophthalmoplegia MELAS NMDA receptor encephalitis Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Malignant hyperthermia of anesthesia Muscular dystrophy Hypokalemic periodic paralysis Neuromyelitis optica spectrum disorder Progressive muscular atrophy Limbic encephalitis with caspr2 antibodies Limbic encephalitis Guillain-Barré syndrome Meningioma Primary angiitis of the central nervous system Meningococcal meningitis Persistent idiopathic facial pain 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 Anoctamin-5-related limb-girdle muscular dystrophy R12 Familial Mediterranean fever 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 Late-onset distal myopathy, Markesbery-Griggs type Corticobasal syndrome Kennedy disease Inclusion body myositis Autosomal dominant cerebellar ataxia Myotonie congénitale de Thomsen et Becker Neuropathie optique héréditaire de Leber Glioblastome Sclérose latérale primitive Myopathie nécrosante à médiation auto-immune Polyradiculonévrite inflammatoire démyélinisante chronique Maladie de Behçet Dystonie isolée Spectre du syndrome de l'homme raide Dystrophie musculaire des ceintures autosomique récessive Dystonie dopa-sensible Artériopathie cérébrale autosomique dominant-infarctus sous-cortical-leucoencéphalopathie Glycogénose par déficit en maltase acide Atrophie multisystématisée type parkinsonien Maladie de Wilson Névralgie trigéminale Hypertension intracrânienne idiopathique Sclérose latérale amyotrophique Amylose ATTR héréditaire