Tsuboi Y - Search Results

1

Magnetic resonance imaging and deep brain stimulation.

Uitti RJ, Tsuboi Y, Pooley RA, Putzke JD, Turk MF, Wszolek ZK, Witte RJ, Wharen RE Jr. Uitti RJ, et al. Among authors: tsuboi y. Neurosurgery. 2002 Dec;51(6):1423-28; discussion 1428-31. Neurosurgery. 2002. PMID: 12445347

2

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.

Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L. Wszolek ZK, et al. Among authors: tsuboi y. Neurology. 2000 Dec 26;55(12):1939. doi: 10.1212/wnl.55.12.1939. Neurology. 2000. PMID: 11134413 No abstract available.

3

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: tsuboi y. Brain. 2001 Aug;124(Pt 8):1666-70. doi: 10.1093/brain/124.8.1666. Brain. 2001. PMID: 11459757 No abstract available.

4

Identifying genetic factors in Parkinson disease.

Farrer M, Hardy J, Hutton M, Maraganore D, Tsuboi Y, Wszolek ZK. Farrer M, et al. Among authors: tsuboi y. JAMA. 2002 Feb 13;287(6):715-6. doi: 10.1001/jama.287.6.715-a. JAMA. 2002. PMID: 11851532 No abstract available.

5

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

6

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

7

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.

8

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.

9

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. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774

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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