Tsuboi Y - Search Results

1

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

Furtado S, Payami H, Lockhart PJ, Hanson M, Nutt JG, Singleton AA, Singleton A, Bower J, Utti RJ, Bird TD, de la Fuente-Fernandez R, Tsuboi Y, Klimek ML, Suchowersky O, Hardy J, Calne DB, Wszolek ZK, Farrer M, Gwinn-Hardy K, Stoessl AJ. Furtado S, et al. Among authors: tsuboi y. Mov Disord. 2004 Jun;19(6):622-9. doi: 10.1002/mds.20074. Mov Disord. 2004. PMID: 15197699 Review.

2

SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.

Furtado S, Farrer M, Tsuboi Y, Klimek ML, de la Fuente-Fernández R, Hussey J, Lockhart P, Calne DB, Suchowersky O, Stoessl AJ, Wszolek ZK. Furtado S, et al. Among authors: tsuboi y. Neurology. 2002 Nov 26;59(10):1625-7. doi: 10.1212/01.wnl.0000035625.19871.dc. Neurology. 2002. PMID: 12451209 Clinical Trial.

3

Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci.

Krygowska-Wajs A, Hussey JM, Hulihan M, Farrer MJ, Tsuboi Y, Uitti RJ, Wszolek ZK. Krygowska-Wajs A, et al. Among authors: tsuboi y. Parkinsonism Relat Disord. 2003 Mar;9(4):193-200. doi: 10.1016/s1353-8020(02)00036-6. Parkinsonism Relat Disord. 2003. PMID: 12618053

4

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).

Wszolek ZK, Tsuboi Y, Ghetti B, Pickering-Brown S, Baba Y, Cheshire WP. Wszolek ZK, et al. Among authors: tsuboi y. Orphanet J Rare Dis. 2006 Aug 9;1:30. doi: 10.1186/1750-1172-1-30. Orphanet J Rare Dis. 2006. PMID: 16899117 Free PMC article. Review.

5

A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy.

Araki E, Tsuboi Y, Daechsel J, Milnerwood A, Vilarino-Guell C, Fujii N, Mishima T, Oka T, Hara H, Fukae J, Farrer MJ. Araki E, et al. Among authors: tsuboi y. Mov Disord. 2014 Aug;29(9):1201-4. doi: 10.1002/mds.25833. Epub 2014 Feb 22. Mov Disord. 2014. PMID: 24676999

6

Japanese family with parkinsonism, depression, weight loss, and central hypoventilation.

Tsuboi Y, Wszolek ZK, Kusuhara T, Doh-ura K, Yamada T. Tsuboi Y, et al. Neurology. 2002 Apr 9;58(7):1025-30. doi: 10.1212/wnl.58.7.1025. Neurology. 2002. PMID: 11940687

7

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

Wszolek ZK, Pfeiffer RF, Tsuboi Y, Uitti RJ, McComb RD, Stoessl AJ, Strongosky AJ, Zimprich A, Müller-Myhsok B, Farrer MJ, Gasser T, Calne DB, Dickson DW. Wszolek ZK, et al. Among authors: tsuboi y. Neurology. 2004 May 11;62(9):1619-22. doi: 10.1212/01.wnl.0000125015.06989.db. Neurology. 2004. PMID: 15136696

8

Clinical-electrophysiological correlation of tremor and myoclonus in a kindred with the N279K tau mutation.

Caviness JN, Tsuboi Y, Wszolek ZK. Caviness JN, et al. Among authors: tsuboi y. Parkinsonism Relat Disord. 2003 Jan;9(3):151-7. doi: 10.1016/s1353-8020(02)00034-2. Parkinsonism Relat Disord. 2003. PMID: 12573870

9

Hereditary tauopathies and parkinsonism.

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

10

Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17.

Cheshire WP, Tsuboi Y, Wszolek ZK. Cheshire WP, et al. Among authors: tsuboi y. Auton Neurosci. 2002 Nov 29;102(1-2):71-7. doi: 10.1016/s1566-0702(02)00205-9. Auton Neurosci. 2002. PMID: 12492138

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