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Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene.
Shimizu H, Toyoshima Y, Shiga A, Yokoseki A, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H. Shimizu H, et al. Among authors: sekine y. Acta Neuropathol. 2013 Sep;126(3):453-9. doi: 10.1007/s00401-013-1150-5. Epub 2013 Jun 28. Acta Neuropathol. 2013. PMID: 23812289
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: sekine y. Neurology. 2016 May 24;86(21):1964-74. doi: 10.1212/WNL.0000000000002694. Epub 2016 Apr 27. Neurology. 2016. PMID: 27164673
Characteristic features and progression of abnormalities on MRI for CARASIL.
Nozaki H, Sekine Y, Fukutake T, Nishimoto Y, Shimoe Y, Shirata A, Yanagawa S, Hirayama M, Tamura M, Nishizawa M, Onodera O. Nozaki H, et al. Among authors: sekine y. Neurology. 2015 Aug 4;85(5):459-63. doi: 10.1212/WNL.0000000000001803. Epub 2015 Jul 2. Neurology. 2015. PMID: 26138950
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: sekine y. J Clin Invest. 2021 Nov 15;131(22):e140555. doi: 10.1172/JCI140555. J Clin Invest. 2021. PMID: 34779414 Free PMC article.
1,003 results