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Renal histopathological findings of retinal vasculopathy with cerebral leukodystrophy.
Tsubata Y, Morita T, Morioka T, Sasagawa T, Ikarashi K, Saito N, Shimada H, Miyazaki S, Sakai S, Tanaka H, Saito R, Toyoshima Y, Nozaki H, Narita I. Tsubata Y, et al. Among authors: nozaki h. CEN Case Rep. 2018 May;7(1):83-89. doi: 10.1007/s13730-017-0300-3. Epub 2018 Jan 10. CEN Case Rep. 2018. PMID: 29322432 Free PMC article.
Candesartan prevents arteriopathy progression in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy model.
Kato T, Manabe RI, Igarashi H, Kametani F, Hirokawa S, Sekine Y, Fujita N, Saito S, Kawashima Y, Hatano Y, Ando S, Nozaki H, Sugai A, Uemura M, Fukunaga M, Sato T, Koyama A, Saito R, Sugie A, Toyoshima Y, Kawata H, Murayama S, Matsumoto M, Kakita A, Hasegawa M, Ihara M, Kanazawa M, Nishizawa M, Tsuji S, Onodera O. Kato T, et al. Among authors: nozaki h. J Clin Invest. 2021 Nov 15;131(22):e140555. doi: 10.1172/JCI140555. J Clin Invest. 2021. PMID: 34779414 Free PMC article.
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.
[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.
Duplication and deletion upstream of LMNB1 in autosomal dominant adult-onset leukodystrophy.
Mezaki N, Miura T, Ogaki K, Eriguchi M, Mizuno Y, Komatsu K, Yamazaki H, Suetsugi N, Kawajiri S, Yamasaki R, Ishiguro T, Konno T, Nozaki H, Kasuga K, Okuma Y, Kira JI, Hara H, Onodera O, Ikeuchi T. Mezaki N, et al. Among authors: nozaki h. Neurol Genet. 2018 Dec 7;4(6):e292. doi: 10.1212/NXG.0000000000000292. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30697589 Free PMC article.
530 results