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A survey on the patient journey in Fabry disease in Japan.
Tsurumi M, Ozaki A, Eto Y. Tsurumi M, et al. Among authors: eto y. Mol Genet Metab Rep. 2022 Aug 17;33:100909. doi: 10.1016/j.ymgmr.2022.100909. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36035889 Free PMC article.
Frequency of de novo mutations in Japanese patients with Fabry disease.
Kobayashi M, Ohashi T, Iizuka S, Kaneshiro E, Higuchi T, Eto Y, Ida H. Kobayashi M, et al. Among authors: eto y. Mol Genet Metab Rep. 2014 Aug 2;1:283-287. doi: 10.1016/j.ymgmr.2014.07.001. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896102 Free PMC article.
Pharmacokinetics and pharmacodynamics of JR-051, a biosimilar of agalsidase beta, in healthy adults and patients with Fabry disease: Phase I and II/III clinical studies.
Nakamura K, Kawashima S, Tozawa H, Yamaoka M, Yamamoto T, Tanaka N, Yamamoto R, Okuyama T, Eto Y. Nakamura K, et al. Among authors: eto y. Mol Genet Metab. 2020 Jul;130(3):215-224. doi: 10.1016/j.ymgme.2020.04.003. Epub 2020 May 1. Mol Genet Metab. 2020. PMID: 32389574 Free article. Clinical Trial.
The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.
Hossain MA, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, Itagaki R, Eto K, Iwamoto T, Yokoi T, Kurosawa K, Numabe H, Eto Y. Hossain MA, et al. Among authors: eto y, eto k. Mol Genet Metab. 2017 Mar;120(3):173-179. doi: 10.1016/j.ymgme.2017.01.002. Epub 2017 Jan 7. Mol Genet Metab. 2017. PMID: 28087245
583 results