Nozaki H - Search Results

1

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes.

Takeuchi R, Tada M, Shiga A, Toyoshima Y, Konno T, Sato T, Nozaki H, Kato T, Horie M, Shimizu H, Takebayashi H, Onodera O, Nishizawa M, Kakita A, Takahashi H. Takeuchi R, et al. Among authors: nozaki h. Acta Neuropathol Commun. 2016 Jun 23;4(1):61. doi: 10.1186/s40478-016-0335-2. Acta Neuropathol Commun. 2016. PMID: 27338935 Free PMC article.

2

[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.

3

[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.

4

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.

5

[Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL)].

Uemura M, Nozaki H, Onodera O. Uemura M, et al. Among authors: nozaki h. Brain Nerve. 2017 Jan;69(1):25-33. doi: 10.11477/mf.1416200631. Brain Nerve. 2017. PMID: 28126975 Japanese.

6

Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease.

Saito N, Ishihara T, Kasuga K, Nishida M, Ishiguro T, Nozaki H, Shimohata T, Onodera O, Nishizawa M. Saito N, et al. Among authors: nozaki h. Prion. 2018 Mar 4;12(2):147-149. doi: 10.1080/19336896.2018.1436926. Epub 2018 Mar 9. Prion. 2018. PMID: 29411683 Free PMC article.

7

Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation.

Ito J, Nozaki H, Toyoshima Y, Abe T, Sato A, Hashidate H, Igarashi S, Onodera O, Takahashi H, Kakita A. Ito J, et al. Among authors: nozaki h. Neuropathology. 2018 May 25. doi: 10.1111/neup.12473. Online ahead of print. Neuropathology. 2018. PMID: 29797751

8

Retinal Vasculopathy With Cerebral Leukodystrophy: Clinicopathologic Features of an Autopsied Patient With a Heterozygous TREX 1 Mutation.

Saito R, Nozaki H, Kato T, Toyoshima Y, Tanaka H, Tsubata Y, Morioka T, Horikawa Y, Oyanagi K, Morita T, Onodera O, Kakita A. Saito R, et al. Among authors: nozaki h. J Neuropathol Exp Neurol. 2019 Feb 1;78(2):181-186. doi: 10.1093/jnen/nly115. J Neuropathol Exp Neurol. 2019. PMID: 30561700

9

Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.

Shiga A, Nozaki H, Yokoseki A, Nihonmatsu M, Kawata H, Kato T, Koyama A, Arima K, Ikeda M, Katada S, Toyoshima Y, Takahashi H, Tanaka A, Nakano I, Ikeuchi T, Nishizawa M, Onodera O. Shiga A, et al. Among authors: nozaki h. Hum Mol Genet. 2011 May 1;20(9):1800-10. doi: 10.1093/hmg/ddr063. Epub 2011 Feb 14. Hum Mol Genet. 2011. PMID: 21320870

10

[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.

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