SE-ATLAS

Manganese poisoning Hereditary ataxia Rare parkinsonian disorder Spastic ataxia Rare parkinsonian syndrome due to intoxication Cyanide-induced parkinsonism-dystonia Autosomal recessive cerebellar ataxia Cerebellar ataxia-hypogonadism syndrome X-linked cerebellar ataxia Delayed encephalopathy due to carbon monoxide poisoning Adult-onset dystonia-parkinsonism Ataxia-tapetoretinal degeneration syndrome Ataxia-hypogonadism-choroidal dystrophy syndrome Primary lateral sclerosis Ataxia-photosensitivity-short stature syndrome Frontotemporal neurodegeneration with movement disorder Non-hereditary degenerative ataxia Autosomal dominant cerebellar ataxia Young-onset Parkinson disease Acquired ataxia Multiple system atrophy Postencephalitic parkinsonism Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome Hereditary late-onset Parkinson disease Rare tremor disorder Atypical juvenile parkinsonism Caribbean parkinsonism Perry syndrome Parkinsonian-pyramidal syndrome Rare ataxia ATP13A2-related juvenile neuronal ceroid lipofuscinosis Dystonia 16 NMDA receptor encephalitis Progressive muscular atrophy Autosomal dominant striatal neurodegeneration Encephalitis lethargica Primary progressive freezing gait X-linked dystonia-parkinsonism Motor neuron disease Genetic motor neuron disease Syndrome parkinsonien et spasticité liés à l'X Maladie acquise du motoneurone Dystonie-parkinsonisme infantile Dystonie-parkinsonisme à début rapide Atrophie multisystématisée type parkinsonien Syndrome parkinsonien rare dû à une maladie neurodégénérative Syndrome de parkinsonisme précoce-déficience intellectuelle Syndrome de Kufor-Rakeb Syndrome d'hémiparkinsonisme-hémiatrophie Maladie de Creutzfeldt-Jakob sporadique