Ishihara T - Search Results

1

Depression and psychiatric symptoms preceding onset of dementia in a family with early-onset Alzheimer disease with a novel PSEN1 mutation.

Kasuga K, Ohno T, Ishihara T, Miyashita A, Kuwano R, Onodera O, Nishizawa M, Ikeuchi T. Kasuga K, et al. Among authors: ishihara t. J Neurol. 2009 Aug;256(8):1351-3. doi: 10.1007/s00415-009-5096-4. Epub 2009 Mar 12. J Neurol. 2009. PMID: 19280102 No abstract available.

2

New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2.

Takagi M, Ozawa T, Hara K, Naruse S, Ishihara T, Shimbo J, Igarashi S, Tanaka K, Onodera O, Nishizawa M. Takagi M, et al. Among authors: ishihara t. Neurology. 2006 Apr 25;66(8):1251-2. doi: 10.1212/01.wnl.0000208415.90685.cd. Neurology. 2006. PMID: 16636245

3

Atypical micrographia associated with corticostriatal white matter lesions in systemic lupus erythematosus.

Ishihara T, Ozawa T, Otsuki M, Shimbo J, Tanaka K, Nishizawa M. Ishihara T, et al. J Neurol Neurosurg Psychiatry. 2006 Aug;77(8):993-4. doi: 10.1136/jnnp.2005.083634. J Neurol Neurosurg Psychiatry. 2006. PMID: 16844958 Free PMC article. No abstract available.

4

[The implications of TDP-43 mutations in pathogenesis of amyotrophic lateral sclerosis].

Ishihara T, Yokoseki A, Nishizawa M, Takahashi H, Onodera O. Ishihara T, et al. Brain Nerve. 2009 Nov;61(11):1301-7. Brain Nerve. 2009. PMID: 19938687 Review. Japanese.

5

Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity.

Fu YJ, Nishihira Y, Kuroda S, Toyoshima Y, Ishihara T, Shinozaki M, Miyashita A, Piao YS, Tan CF, Tani T, Koike R, Iwanaga K, Tsujihata M, Onodera O, Kuwano R, Nishizawa M, Kakita A, Ikeuchi T, Takahashi H. Fu YJ, et al. Among authors: ishihara t. Acta Neuropathol. 2010 Jul;120(1):21-32. doi: 10.1007/s00401-010-0649-2. Epub 2010 Feb 7. Acta Neuropathol. 2010. PMID: 20140439

6

Sleep apnea associated with floppy epiglottis in adult-onset Alexander disease: a case report.

Ishikawa M, Shimohata T, Ishihara T, Nakayama H, Tomita M, Nishizawa M. Ishikawa M, et al. Among authors: ishihara t. Mov Disord. 2010 Jun 15;25(8):1098-100. doi: 10.1002/mds.23042. Mov Disord. 2010. PMID: 20535827 No abstract available.

7

The phenotype spectrum of Japanese multiple system atrophy.

Ozawa T, Tada M, Kakita A, Onodera O, Tada M, Ishihara T, Morita T, Shimohata T, Wakabayashi K, Takahashi H, Nishizawa M. Ozawa T, et al. Among authors: ishihara t. J Neurol Neurosurg Psychiatry. 2010 Nov;81(11):1253-5. doi: 10.1136/jnnp.2009.182576. Epub 2010 Jun 22. J Neurol Neurosurg Psychiatry. 2010. PMID: 20571046

8

Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.

Yokoseki A, Ishihara T, Koyama A, Shiga A, Yamada M, Suzuki C, Sekijima Y, Maruta K, Tsuchiya M, Date H, Sato T, Tada M, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. Yokoseki A, et al. Among authors: ishihara t. Brain. 2011 May;134(Pt 5):1387-99. doi: 10.1093/brain/awr069. Epub 2011 Apr 12. Brain. 2011. PMID: 21486904

9

[Clinical and pathological spectrum of TDP-43 associated ALS].

Onodera O, Yokoseki A, Tan CF, Ishihara T, Nishiira Y, Toyoshima Y, Kakita A, Nishizawa M, Takahashi H. Onodera O, et al. Among authors: ishihara t. Rinsho Shinkeigaku. 2010 Nov;50(11):940-2. doi: 10.5692/clinicalneurol.50.940. Rinsho Shinkeigaku. 2010. PMID: 21921519 Review. Japanese.

10

[FTLD/ALS as TDP-43 proteinopathies].

Ishihara T, Ariizumi Y, Shiga A, Yokoseki A, Sato T, Toyoshima Y, Kakita A, Takahashi H, Nishizawa M, Onodera O. Ishihara T, et al. Rinsho Shinkeigaku. 2010 Nov;50(11):1022-4. doi: 10.5692/clinicalneurol.50.1022. Rinsho Shinkeigaku. 2010. PMID: 21921552 Review. Japanese.

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