Nozaki H - Search Results

1

Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.

Hasegawa A, Ikeuchi T, Koike R, Matsubara N, Tsuchiya M, Nozaki H, Homma A, Idezuka J, Nishizawa M, Onodera O. Hasegawa A, et al. Among authors: nozaki h. Mov Disord. 2010 Aug 15;25(11):1694-700. doi: 10.1002/mds.23167. Mov Disord. 2010. PMID: 20589872

2

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O. Nozaki H, et al. Mov Disord. 2007 Apr 30;22(6):857-62. doi: 10.1002/mds.21443. Mov Disord. 2007. PMID: 17357132

3

Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.

Kaneko H, Kakita A, Kasuga K, Nozaki H, Ishikawa A, Miyashita A, Kuwano R, Ito G, Iwatsubo T, Takahashi H, Nishizawa M, Onodera O, Sisodia SS, Ikeuchi T. Kaneko H, et al. Among authors: nozaki h. J Neurosci. 2007 Nov 28;27(48):13092-7. doi: 10.1523/JNEUROSCI.4244-07.2007. J Neurosci. 2007. PMID: 18045903 Free PMC article.

4

Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations.

Ikeuchi T, Kaneko H, Miyashita A, Nozaki H, Kasuga K, Tsukie T, Tsuchiya M, Imamura T, Ishizu H, Aoki K, Ishikawa A, Onodera O, Kuwano R, Nishizawa M. Ikeuchi T, et al. Among authors: nozaki h. Dement Geriatr Cogn Disord. 2008;26(1):43-9. doi: 10.1159/000141483. Epub 2008 Jun 28. Dement Geriatr Cogn Disord. 2008. PMID: 18587238

5

[Dementia: progress in diagnosis and treatment; Topics, V. Recent topics; 4. Detection of novel dementia-related genes; 2) Dysregulation of TGF-beta family signaling and hereditary cerebral small vessel disease: insight into molecular pathogenesis of CARASIL].

Nozaki H, Nishizawa M, Onodera O. Nozaki H, et al. Nihon Naika Gakkai Zasshi. 2011 Aug 10;100(8):2207-13. doi: 10.2169/naika.100.2207. Nihon Naika Gakkai Zasshi. 2011. PMID: 21899153 Review. Japanese. No abstract available.

6

[Hereditary cerebral small-vessel disease].

Nozaki H, Nishizawa M, Onodera O. Nozaki H, et al. Nihon Rinsho. 2013 Mar;71(3):545-54. Nihon Rinsho. 2013. PMID: 23631251 Review. Japanese.

7

Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

Nozaki H, Nishizawa M, Onodera O. Nozaki H, et al. Stroke. 2014 Nov;45(11):3447-53. doi: 10.1161/STROKEAHA.114.004236. Epub 2014 Aug 12. Stroke. 2014. PMID: 25116877 Review. No abstract available.

8

Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.

Hara K, Shimbo J, Nozaki H, Kikugawa K, Onodera O, Nishizawa M. Hara K, et al. Among authors: nozaki h. Mov Disord. 2007 Jul 15;22(9):1362-3. doi: 10.1002/mds.21557. Mov Disord. 2007. PMID: 17516465 No abstract available.

9

[Molecular pathogenesis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy].

Shiga A, Nozaki H, Nishizawa M, Onodera O. Shiga A, et al. Among authors: nozaki h. Brain Nerve. 2010 Jun;62(6):595-9. Brain Nerve. 2010. PMID: 20548119 Review. Japanese.

10

Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.

Konno T, Yoshida K, Mizuno T, Kawarai T, Tada M, Nozaki H, Ikeda SI, Nishizawa M, Onodera O, Wszolek ZK, Ikeuchi T. Konno T, et al. Among authors: nozaki h. Eur J Neurol. 2017 Jan;24(1):37-45. doi: 10.1111/ene.13125. Epub 2016 Sep 29. Eur J Neurol. 2017. PMID: 27680516 Free PMC article.

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