Takahashi K - Search Results

1

[CADASIL: clinical analysis of CADASIL and CADASIL-like disorders in Japan].

Uchino M, Uyama E, Maeda Y, Hirano T, Suenaga A, Yamada H, Hashimoto Y, Kotorii S, Takahashi K, Tabira T. Uchino M, et al. Among authors: takahashi k. Rinsho Shinkeigaku. 2000 Dec;40(12):1247-50. Rinsho Shinkeigaku. 2000. PMID: 11464469 Review. Japanese.

2

Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Kamimura K, Takahashi K, Uyama E, Tokunaga M, Kotorii S, Uchino M, Tabira T. Kamimura K, et al. Among authors: takahashi k. Alzheimer Dis Assoc Disord. 1999 Oct-Dec;13(4):222-5. doi: 10.1097/00002093-199910000-00008. Alzheimer Dis Assoc Disord. 1999. PMID: 10609671

3

Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.

Uyama E, Tokunaga M, Suenaga A, Kotorii S, Kamimura K, Takahashi K, Tabira T, Uchino M. Uyama E, et al. Among authors: takahashi k. Intern Med. 2000 Sep;39(9):732-7. doi: 10.2169/internalmedicine.39.732. Intern Med. 2000. PMID: 10969905 Free article.

4

[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: takahashi k. Rinsho Shinkeigaku. 2001 Feb-Mar;41(2-3):144-6. Rinsho Shinkeigaku. 2001. PMID: 11481859 Japanese.

5

Mutations of the notch3 gene in non-caucasian patients with suspected CADASIL syndrome.

Kotorii S, Takahashi K, Kamimura K, Nishio T, Arima K, Yamada H, Uyama E, Uchino M, Suenaga A, Matsumoto M, Kuchel G, Rouleau GA, Tabira T. Kotorii S, et al. Among authors: takahashi k. Dement Geriatr Cogn Disord. 2001 May-Jun;12(3):185-93. doi: 10.1159/000051256. Dement Geriatr Cogn Disord. 2001. PMID: 11244211

6

Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.

Oki K, Nagata E, Ishiko A, Shimizu A, Tanaka K, Takahashi K, Tabira T, Katayama T, Suzuki N. Oki K, et al. Among authors: takahashi k. Eur J Neurol. 2007 Apr;14(4):464-6. doi: 10.1111/j.1468-1331.2007.01641.x. Eur J Neurol. 2007. PMID: 17389000

7

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: takahashi k. Ann Neurol. 2001 Jul;50(1):117-20. doi: 10.1002/ana.1083. Ann Neurol. 2001. PMID: 11456301

8

Hydrocephalus, corneal opacities, deafness, valvular heart disease, deformed toes and leptomeningeal fibrous thickening in adult siblings: a new syndrome associated with beta-glucocerebrosidase deficiency and a mosaic population of storage cells.

Uyama E, Takahashi K, Owada M, Okamura R, Naito M, Tsuji S, Kawasaki S, Araki S. Uyama E, et al. Among authors: takahashi k. Acta Neurol Scand. 1992 Oct;86(4):407-20. doi: 10.1111/j.1600-0404.1992.tb05109.x. Acta Neurol Scand. 1992. PMID: 1333717

9

Mutational analysis of intrinsic regions of presenilin 2 that determine its endoproteolytic cleavage and pathological function.

Shirotani K, Takahashi K, Araki W, Maruyama K, Tabira T. Shirotani K, et al. Among authors: takahashi k. J Biol Chem. 2000 Feb 4;275(5):3681-6. doi: 10.1074/jbc.275.5.3681. J Biol Chem. 2000. PMID: 10652366 Free article.

10

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: takahashi k. Neurology. 2000 May 9;54(9):1787-95. doi: 10.1212/wnl.54.9.1787. Neurology. 2000. PMID: 10802785

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