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Variant Alzheimer's Disease with Spastic Paraparesis and Supranuclear Gaze Palsy

  • Namita Sinha (a1), David Grimes (a2), Shinya Tokuhiro (a3), Christine Sato (a3), Ekaterina Rogaeva (a3) and John Woulfe (a4)...
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Copyright

Corresponding author

Division of Anatomical Pathology, Queen Elizabeth II Health Sciences Centre and Dalhousie University, Mackenzie Building, 5788 University Avenue, Halifax, Nova Scotia, B3H 1V8, Canada. Email: drnamitasinha1@gmail.com.

References

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1. Rogaeva, E. The solved and unsolved mysteries of the genetics of early-onset Alzheimer’s disease. Neuromol Med. 2002;2(1):110.
2. Rogaeva, E, Bergeron, C, Sato, C, et al. PS1 Alzheimer’s disease family with spastic paraplegia: the search for a gene modifier. Neurology. 2003;61(7):1005–7.
3. Hanein, S, Martin, E, Boukhris, A, et al. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet. 2008;82(4):9921002.
4. O’Riordan, S, McMonagle, P, Janssen, JC, et al. Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities. Neurology. 2002;59(7):110810
5. Grewal, KK, Stefanelli, MG, Meijer, IA, Hand, CK, Rouleau, GA, Ives, EJ. A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy. Am J Med Genet A. 2004;131(3):249–54.

Variant Alzheimer's Disease with Spastic Paraparesis and Supranuclear Gaze Palsy

  • Namita Sinha (a1), David Grimes (a2), Shinya Tokuhiro (a3), Christine Sato (a3), Ekaterina Rogaeva (a3) and John Woulfe (a4)...

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