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Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
Takei J, Higuchi Y, Ando M, Yoshimura A, Yuan JH, Fujisaki N, Tokashiki T, Kanzato N, Jonosono M, Sueyoshi T, Kanda N, Matsuoka H, Okubo R, Suehara M, Matsuura E, Takashima H. Takei J, et al. Among authors: yuan jh. Front Neurol. 2023 Aug 23;14:1241678. doi: 10.3389/fneur.2023.1241678. eCollection 2023. Front Neurol. 2023. PMID: 37681004 Free PMC article.
Partial deficiency of emerin caused by a splice site mutation in EMD.
Yuan J, Ando M, Higuchi I, Sakiyama Y, Matsuura E, Michizono K, Watanabe O, Nagano S, Inamori Y, Hashiguchi A, Higuchi Y, Yoshimura A, Takashima H. Yuan J, et al. Intern Med. 2014;53(14):1563-8. doi: 10.2169/internalmedicine.53.8922. Epub 2014 Jul 15. Intern Med. 2014. PMID: 25030574 Free article.
Phenotypic variability in childhood of skeletal muscle sodium channelopathies.
Yoshinaga H, Sakoda S, Shibata T, Akiyama T, Oka M, Yuan JH, Takashima H, Takahashi MP, Kitamura T, Murakami N, Kobayashi K. Yoshinaga H, et al. Among authors: yuan jh. Pediatr Neurol. 2015 May;52(5):504-8. doi: 10.1016/j.pediatrneurol.2015.01.014. Epub 2015 Jan 29. Pediatr Neurol. 2015. PMID: 25724373
New type of encephalomyelitis responsive to trimethoprim/sulfamethoxazole treatment in Japan.
Sakiyama Y, Kanda N, Higuchi Y, Yoshimura M, Wakaguri H, Takata Y, Watanabe O, Yuan J, Tashiro Y, Saigo R, Nozuma S, Yoshimura A, Arishima S, Ikeda K, Shinohara K, Arata H, Michizono K, Higashi K, Hashiguchi A, Okamoto Y, Hirano R, Shiraishi T, Matsuura E, Okubo R, Higuchi I, Goto M, Hirano H, Sano A, Iwasaki T, Matsuda F, Izumo S, Takashima H. Sakiyama Y, et al. Neurol Neuroimmunol Neuroinflamm. 2015 Aug 13;2(5):e143. doi: 10.1212/NXI.0000000000000143. eCollection 2015 Oct. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 26309903 Free PMC article.
311 results