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Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study.
Chong PF, Torisu H, Yasumoto S, Okumura A, Mori H, Sato T, Kimura J, Ohga S, Tanaka-Taya K, Kira R; Acute Flaccid Myelitis Collaborative Study Investigators. Chong PF, et al. Among authors: sato t. Clin Neurophysiol. 2021 Oct;132(10):2456-2463. doi: 10.1016/j.clinph.2021.07.013. Epub 2021 Jul 27. Clin Neurophysiol. 2021. PMID: 34454273 Free article.
Incidence and risk factors of acute encephalopathy with biphasic seizures in febrile status epilepticus.
Ichinose F, Nakamura T, Kira R, Furuno K, Ishii S, Takamura K, Hashiguchi M, Inoue T, Senju A, Ichimiya Y, Sakakibara T, Sugiyama N, Naitou T, Higuchi N, Togawa M, Torii KI, Toda S, Iwamatsu H, Sato T, Tsurui S, Tanaka H, Motobayashi M, Abe A, Kawaguchi A, Matsuo M. Ichinose F, et al. Among authors: sato t. Brain Dev. 2022 Jan;44(1):36-43. doi: 10.1016/j.braindev.2021.07.004. Epub 2021 Aug 3. Brain Dev. 2022. PMID: 34362595
Clinical aspects and adrenal functions in eleven Japanese children with X-linked adrenoleukodystrophy.
Miyoshi Y, Sakai N, Hamada Y, Tachibana M, Hasegawa Y, Kiyohara Y, Yamada H, Murakami M, Kondou H, Kimura-Ohba S, Mine J, Sato T, Kamio N, Ueda H, Suzuki Y, Shiomi M, Ohta H, Shimozawa N, Ozono K. Miyoshi Y, et al. Among authors: sato t. Endocr J. 2010;57(11):965-72. doi: 10.1507/endocrj.k10e-204. Epub 2010 Sep 16. Endocr J. 2010. PMID: 20859061 Free article.
[Chronic recurrent multifocal osteomyelitis with interstitial myositis].
Nagashima S, Nozawa T, Kizawa T, Kikuchi M, Miyamae T, Imagawa T, Inaba H, Sato T, Hashimoto K, Aida N, Yokota S. Nagashima S, et al. Among authors: sato t. Nihon Rinsho Meneki Gakkai Kaishi. 2013;36(1):52-7. doi: 10.2177/jsci.36.52. Nihon Rinsho Meneki Gakkai Kaishi. 2013. PMID: 23445733 Free article. Japanese.
A genome-wide association study identified PTPN2 as a population-specific susceptibility gene locus for primary biliary cholangitis.
Hitomi Y, Ueno K, Aiba Y, Nishida N, Kono M, Sugihara M, Kawai Y, Kawashima M, Khor SS, Sugi K, Kouno H, Kouno H, Naganuma A, Iwamoto S, Katsushima S, Furuta K, Nikami T, Mannami T, Yamashita T, Ario K, Komatsu T, Makita F, Shimada M, Hirashima N, Yokohama S, Nishimura H, Sugimoto R, Komura T, Ota H, Kojima M, Nakamuta M, Fujimori N, Yoshizawa K, Mano Y, Takahashi H, Hirooka K, Tsuruta S, Sato T, Yamasaki K, Kugiyama Y, Motoyoshi Y, Suehiro T, Saeki A, Matsumoto K, Nagaoka S, Abiru S, Yatsuhashi H, Ito M, Kawata K, Takaki A, Arai K, Arinaga T, Abe M, Harada M, Taniai M, Zeniya M, Ohira H, Shimoda S, Komori A, Tanaka A, Ishigaki K, Nagasaki M, Tokunaga K, Nakamura M. Hitomi Y, et al. Among authors: sato t. Hepatology. 2024 Apr 23. doi: 10.1097/HEP.0000000000000894. Online ahead of print. Hepatology. 2024. PMID: 38652555
A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.
Hara T, Kazuno AA, Toyota T, Ueda J, Shuno T, Mukai J, Sato TA, Matsumoto N, Yoshikawa T, Takata A. Hara T, et al. Among authors: sato ta. Psychiatry Clin Neurosci. 2024 Apr 22. doi: 10.1111/pcn.13669. Online ahead of print. Psychiatry Clin Neurosci. 2024. PMID: 38646907 No abstract available.
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