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cerebellar disorders, the cerebellum: disorders and treatment, fetal cerebellum, dandy–walker malformation, mega cisterna magna, posterior fossa arachnoid cyst, blake's pouch cyst, cerebellar hypoplasia, unilateral cerebellar hypoplasia, pontocerebellar hypoplasia, rhombencephalosynapsis, joubert syndrome, chiari 1, neuroimaging, classification, preterm birth, cerebellum, hemorrhage, glucocorticoids, pain, developmental outcome, autism spectrum disorder, attention deficihyperactivity disorder, posture, purkinje cell, brain development, mouse models, scar, earlonset ataxia, genetics, nexgeneration sequencing, wholexome sequencing, friedreich ataxia, ataxia with oculomotor apraxia, autosomarecessive spastic ataxia charlevoix–saguenay, syne1, cerebellar ataxia, nonprogressive cerebellar ataxia, cerebellar atrophy, cerebellum and cognition, dna repair, aptx, tdp1, pnkp, xrcc1, parp1, genetic, acquired, ataxia, metabolic derangement, krabbe, niemann–pick, wernicke encephalopathy, superficial siderosis, mitochondria, electron transport chain, oxidative phosphorylation, heteroplasmy, spinocerebellar, cerebellar, autosomadominant, drpla, triplet repeat expansion, adult, pediatric
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motor functions
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