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Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.
Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN. Fox NC, et al. Among authors: hutton m. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene.
Harvey RJ, Ellison D, Hardy J, Hutton M, Roques PK, Collinge J, Fox NC, Rossor MN. Harvey RJ, et al. Among authors: hutton m. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):44-9. doi: 10.1136/jnnp.64.1.44. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436726 Free PMC article.
The genetic and pathological classification of familial frontotemporal dementia.
Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, Ozansoy M, Hardy J, Hutton M, Wood NW, Lees AJ, Revesz T, Lantos P, Rossor MN. Morris HR, et al. Among authors: hutton m. Arch Neurol. 2001 Nov;58(11):1813-6. doi: 10.1001/archneur.58.11.1813. Arch Neurol. 2001. PMID: 11708988
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.
Houlden H, Baker M, McGowan E, Lewis P, Hutton M, Crook R, Wood NW, Kumar-Singh S, Geddes J, Swash M, Scaravilli F, Holton JL, Lashley T, Tomita T, Hashimoto T, Verkkoniemi A, Kalimo H, Somer M, Paetau A, Martin JJ, Van Broeckhoven C, Golde T, Hardy J, Haltia M, Revesz T. Houlden H, et al. Among authors: hutton m. Ann Neurol. 2000 Nov;48(5):806-8. Ann Neurol. 2000. PMID: 11079548
Pick's disease is associated with mutations in the tau gene.
Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, Iwatsubo T, Davies Y, Allsop D, Furlong R, Owen F, Hardy J, Mann D, Hutton M. Pickering-Brown S, et al. Among authors: hutton m. Ann Neurol. 2000 Dec;48(6):859-67. Ann Neurol. 2000. PMID: 11117542
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.
Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, Mann D, Lang AE, Bergeron C, Bigio EH, Litvan I, Bhatia KP, Dickson D, Wood NW, Hutton M. Houlden H, et al. Among authors: hutton m. Neurology. 2001 Jun 26;56(12):1702-6. doi: 10.1212/wnl.56.12.1702. Neurology. 2001. PMID: 11425937
482 results