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HTRA1-Related Cerebral Small Vessel Disease: A Review of the Literature.
Uemura M, Nozaki H, Kato T, Koyama A, Sakai N, Ando S, Kanazawa M, Hishikawa N, Nishimoto Y, Polavarapu K, Nalini A, Hanazono A, Kuzume D, Shindo A, El-Ghanem M, Abe A, Sato A, Yoshida M, Ikeuchi T, Mizuta I, Mizuno T, Onodera O. Uemura M, et al. Among authors: mizuta i. Front Neurol. 2020 Jul 3;11:545. doi: 10.3389/fneur.2020.00545. eCollection 2020. Front Neurol. 2020. PMID: 32719647 Free PMC article. Review.
Increasing microbleeds in CADASIL.
Yagi T, Konoeda F, Mizuta I, Mizuno T, Suzuki N. Yagi T, et al. Among authors: mizuta i. Eur Neurol. 2013;69(6):352-3. doi: 10.1159/000348720. Epub 2013 Apr 26. Eur Neurol. 2013. PMID: 23635799 No abstract available.
Definite familial multiple system atrophy with unknown genetics.
Itoh K, Kasai T, Tsuji Y, Saito K, Mizuta I, Harada Y, Sudoh S, Mizuno T, Nakagawa M, Fushiki S. Itoh K, et al. Among authors: mizuta i. Neuropathology. 2014 Jun;34(3):309-13. doi: 10.1111/neup.12092. Epub 2014 Jan 7. Neuropathology. 2014. PMID: 24397755
A Japanese CADASIL kindred with a novel two-base NOTCH3 mutation.
Suda S, Okubo S, Ueda M, Sowa K, Abe A, Aoki J, Muraga K, Suzuki K, Sakamoto Y, Mizuta I, Mizuno T, Kimura K. Suda S, et al. Among authors: mizuta i. Eur J Neurol. 2016 May;23(5):e32-4. doi: 10.1111/ene.12977. Eur J Neurol. 2016. PMID: 27079553 No abstract available.
Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.
Nozaki H, Kato T, Nihonmatsu M, Saito Y, Mizuta I, Noda T, Koike R, Miyazaki K, Kaito M, Ito S, Makino M, Koyama A, Shiga A, Uemura M, Sekine Y, Murakami A, Moritani S, Hara K, Yokoseki A, Kuwano R, Endo N, Momotsu T, Yoshida M, Nishizawa M, Mizuno T, Onodera O. Nozaki H, et al. Among authors: mizuta i. Neurology. 2016 May 24;86(21):1964-74. doi: 10.1212/WNL.0000000000002694. Epub 2016 Apr 27. Neurology. 2016. PMID: 27164673
124 results