Similar articles

• Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).

  Winner B, Uyanik G, Gross C, Lange M, Schulte-Mattler W, Schuierer G, Marienhagen J, Hehr U, Winkler J. Winner B, et al. Arch Neurol. 2004 Jan;61(1):117-21. doi: 10.1001/archneur.61.1.117. Arch Neurol. 2004. PMID: 14732628
• Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

  Zhang SS, Chen Q, Chen XP, Wang JG, Burgunder JM, Shang HF, Burgunder JM, Yang Y. Zhang SS, et al. Mov Disord. 2008 Apr 30;23(6):917-9. doi: 10.1002/mds.21942. Mov Disord. 2008. PMID: 18361476 No abstract available.
• Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.

  Gucuyener K, Hirfanoglu T, Ok I, Cansu A, Serdaroglu A. Gucuyener K, et al. J Child Neurol. 2007 Feb;22(2):214-7. doi: 10.1177/0883073807300293. J Child Neurol. 2007. PMID: 17621486
• [Hereditary spastic paraplegia associated with thin corpus callosum].

  Kasuga K, Nishizawa M. Kasuga K, et al. No To Shinkei. 2003 Sep;55(9):765-70. No To Shinkei. 2003. PMID: 14571838 Review. Japanese. No abstract available.
• [Neuropathology of familial spastic paraplegia].

  Iwabuchi K. Iwabuchi K. Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):227-30. Ryoikibetsu Shokogun Shirizu. 1999. PMID: 10434638 Review. Japanese. No abstract available.