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10. Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families. De Michele G; Lieto M; Galatolo D; Salvatore E; Cocozza S; Barghigiani M; Tessa A; Baldacci J; Pappatà S; Filla A; De Michele G; Santorelli FM Parkinsonism Relat Disord; 2019 Aug; 65():91-96. PubMed ID: 31126790 [TBL] [Abstract][Full Text] [Related]
11. Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family. Palvadeau R; Kaya-Güleç ZE; Şimşir G; Vural A; Öztop-Çakmak Ö; Genç G; Aygün MS; Falay O; Başak AN; Ertan S Neurogenetics; 2020 Jan; 21(1):51-58. PubMed ID: 31741143 [TBL] [Abstract][Full Text] [Related]
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14. [A case of 77-year-old male with spinocerebellar ataxia type 31 with left dominant dystonia]. Saito R; Kikuno S; Maeda M; Uesaka Y; Ida M Rinsho Shinkeigaku; 2014; 54(8):643-7. PubMed ID: 25142535 [TBL] [Abstract][Full Text] [Related]
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17. Novel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease. Chung EJ; Lee WY; Kim JY; Kim JH; Kim GM; Ki CS; Kim IS Mov Disord; 2007 Jun; 22(8):1206-7. PubMed ID: 17394247 [No Abstract] [Full Text] [Related]
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