Tabira T - Search Results

1

A distinct familial presenile dementia with a novel missense mutation in the tau gene.

Iijima M, Tabira T, Poorkaj P, Schellenberg GD, Trojanowski JQ, Lee VM, Schmidt ML, Takahashi K, Nabika T, Matsumoto T, Yamashita Y, Yoshioka S, Ishino H. Iijima M, et al. Among authors: tabira t. Neuroreport. 1999 Feb 25;10(3):497-501. doi: 10.1097/00001756-199902250-00010. Neuroreport. 1999. PMID: 10208578

2

Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia.

Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, Tabira T, Trojanowski JQ, Borson S, Galasko D, Reich S, Quinn B, Schellenberg G, Bird TD. Poorkaj P, et al. Among authors: tabira t. Arch Neurol. 2001 Mar;58(3):383-7. doi: 10.1001/archneur.58.3.383. Arch Neurol. 2001. PMID: 11255441

3

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

Arima K, Kowalska A, Hasegawa M, Mukoyama M, Watanabe R, Kawai M, Takahashi K, Iwatsubo T, Tabira T, Sunohara N. Arima K, et al. Among authors: tabira t. Neurology. 2000 May 9;54(9):1787-95. doi: 10.1212/wnl.54.9.1787. Neurology. 2000. PMID: 10802785

4

Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau gene.

Miyamoto K, Kowalska A, Hasegawa M, Tabira T, Takahashi K, Araki W, Akiguchi I, Ikemoto A. Miyamoto K, et al. Among authors: tabira t. Ann Neurol. 2001 Jul;50(1):117-20. doi: 10.1002/ana.1083. Ann Neurol. 2001. PMID: 11456301

5

Genetic analysis in patients with familial and sporadic frontotemporal dementia: two tau mutations in only familial cases and no association with apolipoprotein epsilon4.

Kowalska A, Asada T, Arima K, Kumakiri C, Kozubski W, Takahashi K, Tabira T. Kowalska A, et al. Among authors: tabira t. Dement Geriatr Cogn Disord. 2001 Nov-Dec;12(6):387-92. doi: 10.1159/000051285. Dement Geriatr Cogn Disord. 2001. PMID: 11598310

6

Microtubule associated protein (tau) gene variability in patients with frontotemporal dementia.

Kowalska A, Takahashi K, Kozubski W, Tabira T. Kowalska A, et al. Among authors: tabira t. Folia Neuropathol. 2002;40(1):1-5. Folia Neuropathol. 2002. PMID: 12121033

7

[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].

Yamada H, Yasuda T, Kotorii S, Takahashi K, Tabira T, Sunada Y. Yamada H, et al. Among authors: tabira t. Rinsho Shinkeigaku. 2001 Feb-Mar;41(2-3):144-6. Rinsho Shinkeigaku. 2001. PMID: 11481859 Japanese.

8

FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10.

Hasegawa M, Smith MJ, Iijima M, Tabira T, Goedert M. Hasegawa M, et al. Among authors: tabira t. FEBS Lett. 1999 Jan 25;443(2):93-6. doi: 10.1016/s0014-5793(98)01696-2. FEBS Lett. 1999. PMID: 9989582 Free article.

9

Familial frontotemporal dementia with a P301L tau mutation in Japan.

Kodama K, Okada S, Iseki E, Kowalska A, Tabira T, Hosoi N, Yamanouchi N, Noda S, Komatsu N, Nakazato M, Kumakiri C, Yazaki M, Sato T. Kodama K, et al. Among authors: tabira t. J Neurol Sci. 2000 May 1;176(1):57-64. doi: 10.1016/s0022-510x(00)00288-4. J Neurol Sci. 2000. PMID: 10865093

10

A novel mutation at position +11 in the intron following exon 10 of the tau gene in FTDP-17.

Kowalska A, Hasegawa M, Miyamoto K, Akiguchi I, Ikemoto A, Takahashi K, Araki W, Tabira T. Kowalska A, et al. Among authors: tabira t. J Appl Genet. 2002;43(4):535-43. J Appl Genet. 2002. PMID: 12441638

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