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25. Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1. Mascalchi M; Tosetti M; Plasmati R; Bianchi MC; Tessa C; Salvi F; Frontali M; Valzania F; Bartolozzi C; Tassinari CA Ann Neurol; 1998 Feb; 43(2):244-52. PubMed ID: 9485066 [TBL] [Abstract][Full Text] [Related]
26. Ataxia without telangiectasia masquerading as benign hereditary chorea. Klein C; Wenning GK; Quinn NP; Marsden CD Mov Disord; 1996 Mar; 11(2):217-20. PubMed ID: 8684395 [TBL] [Abstract][Full Text] [Related]
27. [A parent and a child cases of autosomal dominant spinocerebellar degeneration: high signal intensity in the transverse pontine fibers(cross sign)]. Tomiyasu H No To Shinkei; 2001 Jul; 53(7):686-7. PubMed ID: 11517498 [No Abstract] [Full Text] [Related]
28. [Positron emission tomography and evoked potentials in the early detection of hereditary ataxias]. Nowak A; Holthoff V; Haupt WF Nervenarzt; 1989 May; 60(5):284-7. PubMed ID: 2786999 [No Abstract] [Full Text] [Related]
29. [Five cases of a Joseph disease family with non-REM sleep apnea and MRI study]. Kitamura J; Tsuruta K; Yamamura Y; Kurihara T; Matsukura S Rinsho Shinkeigaku; 1987 Sep; 27(9):1180-4. PubMed ID: 3481567 [No Abstract] [Full Text] [Related]
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31. Focal dystonia as a presenting sign of spinocerebellar ataxia 17. Hagenah JM; Zühlke C; Hellenbroich Y; Heide W; Klein C Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680 [TBL] [Abstract][Full Text] [Related]