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Japanese Leigh syndrome case treated with EPI-743.
Kouga T, Takagi M, Miyauchi A, Shimbo H, Iai M, Yamashita S, Murayama K, Klein MB, Miller G, Goto T, Osaka H. Kouga T, et al. Brain Dev. 2018 Feb;40(2):145-149. doi: 10.1016/j.braindev.2017.08.005. Epub 2017 Sep 12. Brain Dev. 2018. PMID: 28916229
A child with three episodes of reversible splenial lesion.
Kouga T, Iai M, Yamashita S, Aida N, Takanashi J, Osaka H. Kouga T, et al. Neuropediatrics. 2013 Aug;44(4):199-202. doi: 10.1055/s-0032-1330854. Epub 2012 Dec 19. Neuropediatrics. 2013. PMID: 23254571
De novo DNM1 mutations in two cases of epileptic encephalopathy.
Nakashima M, Kouga T, Lourenço CM, Shiina M, Goto T, Tsurusaki Y, Miyatake S, Miyake N, Saitsu H, Ogata K, Osaka H, Matsumoto N. Nakashima M, et al. Among authors: kouga t. Epilepsia. 2016 Jan;57(1):e18-23. doi: 10.1111/epi.13257. Epub 2015 Nov 27. Epilepsia. 2016. PMID: 26611353 Free article.
Gene Therapy in a Mouse Model of Niemann-Pick Disease Type C1.
Kurokawa Y, Osaka H, Kouga T, Jimbo E, Muramatsu K, Nakamura S, Takayanagi Y, Onaka T, Muramatsu SI, Yamagata T. Kurokawa Y, et al. Among authors: kouga t. Hum Gene Ther. 2021 Jun;32(11-12):589-598. doi: 10.1089/hum.2020.175. Epub 2021 Feb 22. Hum Gene Ther. 2021. PMID: 33256498 Free PMC article.
13 results