Chapter 17 Hereditary spastic paraparesis
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Elsevier
Reference195 articles.
1. Disordered pigmentation, spastic paraparesis and peripheral neuropathy in three siblings: a new neurocutaneous syndrome;Abdallat;J Neurol Neurosurg Psychiatry,1980
2. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A;Abel;Neurogenetics,2004
3. Some examples of the inheritance of mental deficiency: apparently sexlinked idiocy and microcephaly;Allan;Am J Ment Defic,1944
4. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia;Ashley-Koch;Neurogenetics,2001
5. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia;Atorino;J Cell Biol,2003
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Gait analysis patterns and rehabilitative interventions to improve gait in persons with hereditary spastic paraplegia: a systematic review and meta-analysis;Frontiers in Neurology;2023-09-20
2. Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations;Neurology Genetics;2018-10-24
3. Effects of superficial heating and insulation on walking speed in people with hereditary and spontaneous spastic paraparesis: A randomised crossover study;Annals of Physical and Rehabilitation Medicine;2018-03
4. The Effects of Dalfampridine on Hereditary Spastic Paraparesis;European Neurology;2016
5. Hereditary spastic paraplegia: up to date;Rinsho Shinkeigaku;2014
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