MING-CHE KUOCHUN-HWEI TAISHENG-HONG TSENGRUEY-MEEI WU2022-09-202022-09-202022-081351-5101https://scholars.lib.ntu.edu.tw/handle/123456789/621675Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant inherited disorder that manifests as a mixture of cerebellar ataxia, parkinsonism, and polyneuropathy; in type IV SCA3, pure parkinsonism is the only symptom. Currently, no disease-modifying treatment is available, but variable responses to antiparkinsonism agents have been reported. However, the benefits of deep brain stimulation (DBS) for treating parkinsonism in this subtype of SCA3 remain unclear.endeep brain stimulation; impulse control disorders; motor complications; parkinsonian disorders; spinocerebellar ataxia[SDGs]SDG310.1111/ene.15339358377532-s2.0-85134005943WOS:000829597600040https://api.elsevier.com/content/abstract/scopus_id/85134005943