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Results 1 - 10 of 14 for Hereditary spastic paraplegia 18
  1. ... of the same family. The prevalence of all hereditary spastic paraplegias combined is estimated to be 1 to 18 in 100,000 people worldwide. Spastic paraplegia type 8 likely accounts for no more than ...
  2. ... Clinical and genetic analysis of Taiwanese patients with hereditary spastic paraplegia type 5. Eur J Neurol. 2015 Jan;22(1):211-4. doi: 10.1111/ene.12407. Epub 2014 Mar 18. Citation on PubMed Tsaousidou MK, Ouahchi K, Warner ...
  3. ... 72. doi: 10.1038/ng1980. Epub 2007 Feb 18. Citation on PubMed
  4. ... of undiagnosed ataxia. Neurology. 2015 May 5;84(18):1911. doi: ... mutations in hereditary spastic paraplegia. Brain. 2004 May;127(Pt 5):973-80. ...
  5. ... of undiagnosed ataxia. Neurology. 2015 May 5;84(18):1911. doi: ... mutations in hereditary spastic paraplegia. Brain. 2004 May;127(Pt 5):973-80. ...
  6. ... literature review. Eur J Paediatr Neurol. 2014 Mar;18(2):235-9. doi: ... hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 ...
  7. Troyer syndrome is a type of hereditary spastic paraplegia, also called hereditary spastic paraparesis. Hereditary spastic paraplegias are a group of genetic disorders characterized by progressive stiffness (spasticity) and weakness of ...
  8. L1 syndrome describes a group of conditions that primarily affect the nervous system and occur almost exclusively in males. These conditions vary in severity ...
  9. ... spastic paraplegia Spastic paraplegia 2 X linked recessive hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia Genetic Testing ...
  10. ... Troyer syndrome. Troyer syndrome is a type of hereditary spastic paraplegia (also called hereditary spastic paraparesis), a group of ... PubMed Lu J, Rashid F, Byrne PC. The hereditary spastic paraplegia protein spartin localises to mitochondria. J Neurochem. 2006 ...
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