Hutton ML - Search Results

1

Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation.

Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L, Hutton ML, Dickson DW. Wszolek ZK, et al. Among authors: hutton ml. Brain. 2001 Aug;124(Pt 8):1666-70. doi: 10.1093/brain/124.8.1666. Brain. 2001. PMID: 11459757 No abstract available.

2

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Tsuboi Y, Uitti RJ, Baker M, Hutton ML, Wszolek ZK. Tsuboi Y, et al. Among authors: hutton ml. Neurology. 2003 Feb 11;60(3):525-6. doi: 10.1212/wnl.60.3.525-b. Neurology. 2003. PMID: 12578950 No abstract available.

3

Hereditary tauopathies and parkinsonism.

Wszolek ZK, Tsuboi Y, Farrer M, Uitti RJ, Hutton ML. Wszolek ZK, et al. Among authors: hutton ml. Adv Neurol. 2003;91:153-63. Adv Neurol. 2003. PMID: 12442674 Review. No abstract available.

4

Progressive supranuclear palsy: pathology and genetics.

Dickson DW, Rademakers R, Hutton ML. Dickson DW, et al. Among authors: hutton ml. Brain Pathol. 2007 Jan;17(1):74-82. doi: 10.1111/j.1750-3639.2007.00054.x. Brain Pathol. 2007. PMID: 17493041 Free PMC article. Review.

5

Haplotype-phenotype correlations in kindreds with the N279K mutation in the tau gene.

Woodruff BK, Baba Y, Hutton ML, Wszolek ZK, Tsuboi Y, Kobayashi T, Ghetti B, Arima K, Yasuda M, Rascol O. Woodruff BK, et al. Among authors: hutton ml. Arch Neurol. 2004 Aug;61(8):1327; author reply 1327. doi: 10.1001/archneur.61.8.1327-a. Arch Neurol. 2004. PMID: 15313857 No abstract available.

6

Atypical progressive supranuclear palsy with corticospinal tract degeneration.

Josephs KA, Katsuse O, Beccano-Kelly DA, Lin WL, Uitti RJ, Fujino Y, Boeve BF, Hutton ML, Baker MC, Dickson DW. Josephs KA, et al. Among authors: hutton ml. J Neuropathol Exp Neurol. 2006 Apr;65(4):396-405. doi: 10.1097/01.jnen.0000218446.38158.61. J Neuropathol Exp Neurol. 2006. PMID: 16691120

7

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.

Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Tsuboi Y, et al. Arch Neurol. 2002 Jun;59(6):943-50. doi: 10.1001/archneur.59.6.943. Arch Neurol. 2002. PMID: 12056930

8

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).

Tsuboi Y, Baker M, Hutton ML, Uitti RJ, Rascol O, Delisle MB, Soulages X, Murrell JR, Ghetti B, Yasuda M, Komure O, Kuno S, Arima K, Sunohara N, Kobayashi T, Mizuno Y, Wszolek ZK. Tsuboi Y, et al. Among authors: hutton ml. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774

9

Autosomal dominant dystonia-plus with cerebral calcifications.

Wszolek ZK, Baba Y, Mackenzie IR, Uitti RJ, Strongosky AJ, Broderick DF, Baker MC, Melquist S, Hutton ML, Tsuboi Y, Allanson JE, Carr J, Kumar A, Calne SM, Miklossy J, McGeer PL, Calne DB, Stoessl AJ. Wszolek ZK, et al. Among authors: hutton ml. Neurology. 2006 Aug 22;67(4):620-5. doi: 10.1212/01.wnl.0000230141.40784.09. Neurology. 2006. PMID: 16924015 Clinical Trial.

10

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. Neurology. 2001 Jun 26;56(12):1702-6. doi: 10.1212/wnl.56.12.1702. Neurology. 2001. PMID: 11425937

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