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Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27).
Saito-Hakoda A, Kikuchi A, Takahashi T, Yokoyama Y, Himori N, Adachi M, Ikeda R, Nomura Y, Takayama J, Kawashima J, Katsuoka F, Fujishima F, Yamaguchi T, Ito A, Hanita T, Kanno J, Aizawa T, Nakazawa T, Kawase T, Tamiya G, Yamamoto M, Fujiwara I, Kure S. Saito-Hakoda A, et al. Among authors: fujishima f. J Bone Miner Metab. 2023 Mar;41(2):193-202. doi: 10.1007/s00774-022-01392-w. Epub 2022 Dec 15. J Bone Miner Metab. 2023. PMID: 36520195 Review.
Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice.
Wada Y, Kikuchi A, Kaga A, Shimizu N, Ito J, Onuma R, Fujishima F, Totsune E, Sato R, Niihori T, Shirota M, Funayama R, Sato K, Nakazawa T, Nakayama K, Aoki Y, Aiba S, Nakagawa K, Kure S. Wada Y, et al. Among authors: fujishima f. PLoS Genet. 2020 Feb 26;16(2):e1008628. doi: 10.1371/journal.pgen.1008628. eCollection 2020 Feb. PLoS Genet. 2020. PMID: 32101538 Free PMC article.
PTOV1: a novel testosterone-induced atherogenic gene in human aorta.
Nakamura Y, Suzuki T, Igarashi K, Kanno J, Furukawa T, Tazawa C, Fujishima F, Miura I, Ando T, Moriyama N, Moriya T, Saito H, Yamada S, Sasano H. Nakamura Y, et al. Among authors: fujishima f. J Pathol. 2006 Aug;209(4):522-31. doi: 10.1002/path.1993. J Pathol. 2006. PMID: 16639697
Gastric Duplication Cyst With Occult GIST Component.
Lee S, Uno K, Fujishima F, Hatta W, Koike T, Aoki T, Tanaka N, Musha H, Kikuchi R, Masamune A. Lee S, et al. Among authors: fujishima f. ACG Case Rep J. 2020 Feb 7;7(2):e00260. doi: 10.14309/crj.0000000000000260. eCollection 2020 Feb. ACG Case Rep J. 2020. PMID: 32309505 Free PMC article.
206 results