Hereditary spastic paraplegia: up to date
Author:
Affiliation:
1. Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi
Publisher
Societas Neurologica Japonica
Subject
Clinical Neurology
Reference5 articles.
1. 1) McDermott CJ, Shaw PJ. Hereditary spastic paraplegia. In: Eisen AA, Shaw PJ, editors. Handbook of Clinical Neurology, Vol 82, Motor neuron disorders and related diseases. Amsterdam: Elsevier Science; 2007. p 327-352,
2. 2) Harding AE. Hereditary “pure” spastic paraplegia: a clinical and genetic study of 22 families. J Neurol Neurosurg Psychiatry 1981;44:871-883.
3. 5) Shimazaki H, Takiyama Y, Ishiura H, et al. A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55). J Med Genet 2012;49:777-784.
4. 6) Shimazaki H, Honda J, Naoi T, et al. Autosomal recessive complicated spastic paraplegia with lysosomal trafficking regulator gene mutation. J Neurol Neurosurg Psychiatry 2014;85:1024-1028.
5. 7) Fink JK. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. Acta Neuropathol 2013;126:307-328.
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