1) Nanri K, Koizumi K, Mitoma H, Taguchi T, Takeguchi M, et al: Classification of cerebellar atrophy using voxel-based morphometry and SPECT with an easy Z-score imaging syatem. Intern Med 49: 535-541, 2010
2) Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, et al: Second consensus statement on the diagnosis of multiple system atrophy. Neurology 71: 670-676, 2008
3) Hirata Y, Matsuda H, Nemoto K, Ohnishi T, Hirao K, et al: Voxel-based morphometry to discriminate early Alzheimer's disease from controls. Neurosci Lett 382: 269-274, 2005
4) Hauser TK, Luft A, Skalej M, Nägele T, Kircher TT, et al: Visualization and quantification of disease progression in multiple system atrophy. Mov Disord 21: 1674-1681, 2006
5) Lukas C, Schöls L, Bellenberg B, Rüb U, Przuntek H, et al: Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study. Neurosci Lett 408: 230-235, 2006
6) Goel G, Pal PK, Ravishankar S, Venkatasubramanian G, Jayakumar PN, et al: Gray matter volume deficits in spinocerebellar ataxia: an optimized voxel based morphometric study. Parkinsonism Relat Disord 17: 521-527, 2011
7) 永井真貴子, 佐久間良: 非遺伝性SCD (OPCA・SDS・SND・LCCA). 阿部康二(編): 新しいSCDの臨床――脊髄小脳変性症の臨床. 新興医学出版社, 東京, 1996, pp39-45
8) Seidel K, Siswanto S, Brunt ER, den Dunnen W, Korf HW, et al: Brain pathology of spinocerebellar ataxias. Acta Neuropathol 124: 1-21, 2012
9) 渡辺光法: Machado-Joseph病. 阿部康二(編): 新しいSCDの臨床――脊髄小脳変性症の臨床. 新興医学出版社, 東京, 1996, pp15-22
10) 高橋昭喜: 脊髄小脳変性症のMRI. 阿部康二(編): 新しいSCDの臨床――脊髄小脳変性症の臨床. 新興医学出版社, 東京, 1996, pp68-80
11) 今野秀彦: 遺伝性脊髄小脳変性症の病理. 阿部康二(編): 新しいSCDの臨床――脊髄小脳変性症の臨床. 新興医学出版社, 東京, 1996, pp59-67
12) Koide R, Onodera O, Ikeuchi T, Kondo R, Tanaka H, et al: Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy: influence of CAG repeat size on MRI findings. Neurology 49: 1605-1612, 1997
13) Ishikawa K, Watanabe M, Yoshizawa K, Fujita T, Iwamoto, H et al: Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6). J Neurol Neurosurg Psychiatry 67: 86-89, 1999
14) Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, et al: A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III. Neurology 65: 629-632, 2005