18-6-3-4　ⓔ文献

  1. McDermott CJ, Shaw PJ: Hereditary spastic paraplegia. Handbook of Clinical Neurology (Eisen AA, Shaw PJ, eds), Vol 82. Motor neuron disorders and related diseases, Elsevier Science, 2007; 198–211.

  2. 瀧山嘉久：遺伝性痙性対麻痺．Annual Review 神経 (柳澤信夫，篠原幸人，他編)，中外医学社，2008; 198–211.

  3. Harding AE: Hereditary “pure” spastic paraplegia: a clinical and genetic study of 22 families. J Neurol Neurosurg Psychiatry, 1981; 44: 871–883.

  4. Familial spinal cord syndromes (SPG). https://neuromuscular.wustl.edu/spinal/fsp.html

  5. Finsterer J, Loscher W, et al: Hereditary spastic paraplegias with autosomal dominant, recessive, X–linked, or maternal trait of inheritance. J Neurol Sci, 2012; 318: 1–18.

  6. Hirayama K, Takayanagi T, et al: Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study. Acta Neurol Scand, 1994; 153: 1–22.

  7. Tsuji S, Onodera O, et al: Sporadic ataxias in Japan: a population–based epidemiological study. Cerebellum, 2008; 7: 189–197.

  8. 瀧山嘉久：Japan Spastic Paraplegia Research Consortium (JASPAC). 脳神経，2014; 66: 1210–1217.

  9. 日本神経学会・厚生労働省 運動失調症の医療基盤に関する調査委員会監，脊髄小脳変性症・多系統萎縮症診療ガイドライン作成委員会編．脊髄小脳変性症・多系統萎縮症診療ガイドライン2018, 南江堂，2018; 95–118.

  10. Lo Giudice T, Lombardi F, et al: Hereditary spastic paraplegia: clinical–genetic characteristics and evolving molecular mechanisms. Exp Neurol, 2014; 261: 518–539.

  11. Namekawa M, Ribai P, et al: SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years. Neurology, 2006; 66: 112–114.

  12. Fink JK: Hereditary spastic paraplegia: clinic–pathologic features and emerging molecular mechanism. Acta Neuropathol, 2013; 126: 307–328.

  13. 瀧山嘉久，三輪道然，他：痙性対麻痺の診断基準の提案．厚生労働省難治性疾患等克服研究事業，運動失調症の病態解明と治療法開発に関する研究班 平成25年度研究報告書，2014; 87–90.

  14. Schule R, Wiethoff S, et al: Hereditary spastic paraplegia: clinicogenetic lessons from 608 patients. Ann Neurol, 2016; 79: 646–658.