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HECW2-related disorder in four Japanese patients.
Yanagishita T, Hirade T, Shimojima Yamamoto K, Funatsuka M, Miyamoto Y, Maeda M, Yanagi K, Kaname T, Nagata S, Nagata M, Ishihara Y, Miyashita Y, Asano Y, Sakata Y, Kosaki K, Yamamoto T. Yanagishita T, et al. Among authors: miyamoto y. Am J Med Genet A. 2021 Oct;185(10):2895-2902. doi: 10.1002/ajmg.a.62363. Epub 2021 May 28. Am J Med Genet A. 2021. PMID: 34047014
Corrigendum to "HECW2-related disorder in four Japanese patients. Am J Med Genet Part A. First published: 28 May 2021 https://doi.org/10.1002/ajmg.a.62363".
Yanagishita T, Hirade T, Yamamoto KS, Funatsuka M, Miyamoto Y, Maeda M, Yanagi K, Kaname T, Nagata S, Nagata M, Ishihara Y, Miyashita Y, Asano Y, Sakata Y, Kosaki K, Yamamoto T. Yanagishita T, et al. Among authors: miyamoto y. Am J Med Genet A. 2021 Dec;185(12):3926-3927. doi: 10.1002/ajmg.a.62414. Epub 2021 Jul 10. Am J Med Genet A. 2021. PMID: 34245093 No abstract available.
HPeV3-associated acute encephalitis/encephalopathy among Japanese infants.
Abe Y, Ohno T, Matsumoto H, Daimon Y, Kurahashi H, Takayama R, Sakaguchi Y, Tanabe S, Tanaka F, Miyamoto Y, Kawano A, Yamanouchi H. Abe Y, et al. Among authors: miyamoto y. Brain Dev. 2021 Apr;43(4):528-537. doi: 10.1016/j.braindev.2020.12.010. Epub 2021 Jan 8. Brain Dev. 2021. PMID: 33423809
High-amplitude fast activity in EEG: An early diagnostic marker in children with beta-propeller protein-associated neurodegeneration (BPAN).
Kidokoro H, Yamamoto H, Kubota T, Motobayashi M, Miyamoto Y, Nakata T, Takano K, Shiba N, Okai Y, Tanaka M, Sakaguchi Y, Maki Y, Kawaguchi M, Suzuki T, Muramatsu K, Natsume J. Kidokoro H, et al. Among authors: miyamoto y. Clin Neurophysiol. 2020 Sep;131(9):2100-2104. doi: 10.1016/j.clinph.2020.06.006. Epub 2020 Jun 25. Clin Neurophysiol. 2020. PMID: 32682237
3,481 results