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Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation.
Miyahara H, Tamai C, Inoue M, Sekiguchi K, Tahara D, Tahara N, Takeda K, Arafuka S, Moriyoshi H, Koizumi R, Akagi A, Riku Y, Sone J, Yoshida M, Ihara K, Iwasaki Y. Miyahara H, et al. Among authors: ihara k. Brain Pathol. 2023 Nov;33(6):e13199. doi: 10.1111/bpa.13199. Epub 2023 Aug 3. Brain Pathol. 2023. PMID: 37534760 Free PMC article.
Comparison of physician- and self-assessed pubertal onset in Japanese children.
Saito-Abe M, Nishizato M, Yamamoto-Hanada K, Yang L, Fukami M, Ito Y, Ihara K, Iwabuchi A, Okamoto S, Naiki Y, Ohya Y, Horikawa R. Saito-Abe M, et al. Among authors: ihara k. Front Pediatr. 2023 Mar 21;11:950541. doi: 10.3389/fped.2023.950541. eCollection 2023. Front Pediatr. 2023. PMID: 37025288 Free PMC article.
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Matsumoto M, Oyake M, Itonaga T, Maeda M, Suenobu S, Sato D, Sasahara Y, Mishima H, Yoshiura KI, Ihara K. Matsumoto M, et al. Among authors: ihara k. Eur J Med Genet. 2024 Apr 15;69:104939. doi: 10.1016/j.ejmg.2024.104939. Online ahead of print. Eur J Med Genet. 2024. PMID: 38614309 Free article.
881 results