Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

277 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Heredofamilial brain calcinosis syndrome.
Baba Y, Broderick DF, Uitti RJ, Hutton ML, Wszolek ZK. Baba Y, et al. Among authors: hutton ml. Mayo Clin Proc. 2005 May;80(5):641-51. doi: 10.4065/80.5.641. Mayo Clin Proc. 2005. PMID: 15887432 Review.
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.
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia.
Baker M, Strongosky AJ, Sanchez-Contreras MY, Yang S, Ferguson W, Calne DB, Calne S, Stoessl AJ, Allanson JE, Broderick DF, Hutton ML, Dickson DW, Ross OA, Wszolek ZK, Rademakers R. Baker M, et al. Among authors: hutton ml. Neurogenetics. 2014 Mar;15(1):23-30. doi: 10.1007/s10048-013-0378-5. Epub 2013 Oct 18. Neurogenetics. 2014. PMID: 24135862 Free PMC article.
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.
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation).
Arvanitakis Z, Witte RJ, Dickson DW, Tsuboi Y, Uitti RJ, Slowinski J, Hutton ML, Lin SC, Boeve BF, Cheshire WP, Pooley RA, Liss JM, Caviness JN, Strongosky AJ, Wszolek ZK. Arvanitakis Z, et al. Among authors: hutton ml. Parkinsonism Relat Disord. 2007 May;13(4):230-9. doi: 10.1016/j.parkreldis.2006.10.007. Epub 2006 Dec 29. Parkinsonism Relat Disord. 2007. PMID: 17196872
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.
Rademakers R, Eriksen JL, Baker M, Robinson T, Ahmed Z, Lincoln SJ, Finch N, Rutherford NJ, Crook RJ, Josephs KA, Boeve BF, Knopman DS, Petersen RC, Parisi JE, Caselli RJ, Wszolek ZK, Uitti RJ, Feldman H, Hutton ML, Mackenzie IR, Graff-Radford NR, Dickson DW. Rademakers R, et al. Among authors: hutton ml. Hum Mol Genet. 2008 Dec 1;17(23):3631-42. doi: 10.1093/hmg/ddn257. Epub 2008 Aug 21. Hum Mol Genet. 2008. PMID: 18723524 Free PMC article.
The effect of tau genotype on clinical features in FTDP-17.
Baba Y, Tsuboi Y, Baker MC, Uitti RJ, Hutton ML, Dickson DW, Farrer M, Putzke JD, Woodruff BK, Ghetti B, Murrell JR, Boeve BF, Petersen RC, Verpillat P, Brice A, Delisle MB, Rascol O, Arima K, Dysken MW, Yasuda M, Kobayashi T, Sunohara N, Komure O, Kuno S, Sperfeld AD, Stoppe G, Kohlhase J, Pickering-Brown S, Neary D, Bugiani O, Wszolek ZK. Baba Y, et al. Among authors: hutton ml. Parkinsonism Relat Disord. 2005 Jun;11(4):205-8. doi: 10.1016/j.parkreldis.2005.01.003. Parkinsonism Relat Disord. 2005. PMID: 15878580
277 results