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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity.
Pippucci T, Panza E, Pompilii E, Donadio V, Borreca A, Babalini C, Patrono C, Zuntini R, Kawarai T, Bernardi G, Liguori R, Romeo G, Montagna P, Orlacchio A, Seri M. Pippucci T, et al. Among authors: kawarai t. Eur J Neurol. 2009 Jan;16(1):121-6. doi: 10.1111/j.1468-1331.2008.02367.x. Eur J Neurol. 2009. PMID: 19087158
Spastic paraplegia in Romania: high prevalence of SPG4 mutations.
Orlacchio A, Patrono C, Borreca A, Babalini C, Bernardi G, Kawarai T. Orlacchio A, et al. Among authors: kawarai t. J Neurol Neurosurg Psychiatry. 2008 May;79(5):606-7. doi: 10.1136/jnnp.2007.128827. Epub 2007 Oct 30. J Neurol Neurosurg Psychiatry. 2008. PMID: 17971434 No abstract available.
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease.
Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, Farrer LA, St Georg-Hyslop P, Rogaeva EA. Nicolaou M, et al. Among authors: kawarai t. Neurogenetics. 2001 Oct;3(4):203-6. doi: 10.1007/s100480100123. Neurogenetics. 2001. PMID: 11714100
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE.
Song YQ, Rogaeva E, Premkumar S, Brindle N, Kawarai T, Orlacchio A, Yu G, Levesque G, Nishimura M, Ikeda M, Pei Y, O'Toole C, Duara R, Barker W, Sorbi S, Freedman M, Farrer L, St George-Hyslop P. Song YQ, et al. Among authors: kawarai t. Neurosci Lett. 1998 Jul 10;250(3):189-92. doi: 10.1016/s0304-3940(98)00470-4. Neurosci Lett. 1998. PMID: 9708864 Free article.
172 results