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Page 1
[Current and future strategies for burnout in Japanese neurologists].
Shimohata T, Kubo M, Aiba I, Hattori N, Yoshida K, Unno Y, Yokoyama K, Ogawa T, Kaseda Y, Koike R, Shimizu Y, Tsuboi Y, Doyu M, Misawa S, Miyachi T, Toda T, Takeda A; Committee for Career Development Promotion, Japanese Society of Neurology. Shimohata T, et al. Among authors: koike r. Rinsho Shinkeigaku. 2021 Feb 23;61(2):89-102. doi: 10.5692/clinicalneurol.cn-001533. Epub 2021 Jan 26. Rinsho Shinkeigaku. 2021. PMID: 33504753 Japanese.
[Burnout in Japanese neurologists: comparison of male and female physicians].
Kubo M, Aiba I, Shimohata T, Hattori N, Yoshida K, Unno Y, Yokoyama K, Ogawa T, Kaseda Y, Koike R, Shimizu Y, Tsuboi Y, Doyu M, Misawa S, Miyachi T, Toda T, Takeda A; Committee for Career Development Promotion, Japanese Society of Neurology. Kubo M, et al. Among authors: koike r. Rinsho Shinkeigaku. 2021 Apr 21;61(4):219-227. doi: 10.5692/clinicalneurol.cn-001569. Epub 2021 Mar 25. Rinsho Shinkeigaku. 2021. PMID: 33762500 Japanese.
Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.
Kuroha Y, Ishiguro T, Tada M, Hara N, Murayama K, Kawachi I, Kasuga K, Miyashita A, Hasegawa A, Takahashi T, Matsubara N, Onodera O, Kakita A, Koike R, Ikeuchi T. Kuroha Y, et al. Among authors: koike r. Neurol Genet. 2022 Sep 27;8(5):e200030. doi: 10.1212/NXG.0000000000200030. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36176336 Free PMC article.
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S. Ishiura H, et al. Among authors: koike r. Nat Genet. 2018 Apr;50(4):581-590. doi: 10.1038/s41588-018-0067-2. Epub 2018 Mar 5. Nat Genet. 2018. PMID: 29507423
Development of a Novel Nutrition-Related Multivariate Biomarker for Mild Cognitive Impairment Based on the Plasma Free Amino Acid Profile.
Ikeuchi T, Yano Y, Sato W, Morikawa F, Toru S, Nishimura C, Miyazawa N, Kuroha Y, Koike R, Tanaka S, Utsumi K, Kasuga K, Tokutake T, Ono K, Yano S, Naruse S, Yajima R, Hamano T, Yokoyama Y, Kitamura A, Kaneko E, Yamakado M, Nagao K. Ikeuchi T, et al. Among authors: koike r. Nutrients. 2022 Feb 1;14(3):637. doi: 10.3390/nu14030637. Nutrients. 2022. PMID: 35276996 Free PMC article.
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: koike r. Neurology. 2016 May 24;86(21):1964-74. doi: 10.1212/WNL.0000000000002694. Epub 2016 Apr 27. Neurology. 2016. PMID: 27164673
22 results