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Did you mean yoshino wada (3 results)?
Editorial.
Wada Y. Wada Y. Mass Spectrom (Tokyo). 2013;2(Spec Iss):K0004. doi: 10.5702/massspectrometry.K0004. Mass Spectrom (Tokyo). 2013. PMID: 24349918 Free PMC article. Review. No abstract available.
L-Fucose treatment of FUT8-CDG.
Park JH, Reunert J, He M, Mealer RG, Noel M, Wada Y, Grüneberg M, Horváth J, Cummings RD, Schwartz O, Marquardt T. Park JH, et al. Among authors: wada y. Mol Genet Metab Rep. 2020 Dec 5;25:100680. doi: 10.1016/j.ymgmr.2020.100680. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33312876 Free PMC article.
Foreword.
Wada Y. Wada Y. Mass Spectrom (Tokyo). 2013;2(Spec Iss):K0005. doi: 10.5702/massspectrometry.K0005. Mass Spectrom (Tokyo). 2013. PMID: 24349919 Free PMC article. Review. No abstract available.
Safety of Amlodipine in Early Pregnancy.
Mito A, Murashima A, Wada Y, Miyasato-Isoda M, Kamiya CA, Waguri M, Yoshimatsu J, Yakuwa N, Watanabe O, Suzuki T, Arata N, Mikami M, Ito S. Mito A, et al. Among authors: wada y. J Am Heart Assoc. 2019 Aug 6;8(15):e012093. doi: 10.1161/JAHA.119.012093. Epub 2019 Jul 26. J Am Heart Assoc. 2019. PMID: 31345083 Free PMC article.
Role of C-mannosylation in the secretion of mindin.
Inai Y, Ueda K, Matsui IL, Tajiri M, Minakata S, Wada Y, Ihara Y. Inai Y, et al. Among authors: wada y. Biochim Biophys Acta Gen Subj. 2020 Aug;1864(8):129632. doi: 10.1016/j.bbagen.2020.129632. Epub 2020 May 19. Biochim Biophys Acta Gen Subj. 2020. PMID: 32416197
Advanced analytical methods for hemoglobin variants.
Wada Y. Wada Y. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Dec 5;781(1-2):291-301. doi: 10.1016/s1570-0232(02)00558-5. J Chromatogr B Analyt Technol Biomed Life Sci. 2002. PMID: 12450664 Review.
Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles.
Okamoto N, Ohto T, Enokizono T, Wada Y, Kohmoto T, Imoto I, Haga Y, Seino J, Suzuki T. Okamoto N, et al. Among authors: wada y. Cells. 2021 Nov 10;10(11):3117. doi: 10.3390/cells10113117. Cells. 2021. PMID: 34831340 Free PMC article.
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature.
Sonoda Y, Fujita A, Torio M, Mukaino T, Sakata A, Matsukura M, Yonemoto K, Hatae K, Ichimiya Y, Chong PF, Ochiai M, Wada Y, Kadoya M, Okamoto N, Murakami Y, Suzuki T, Isobe N, Shigeto H, Matsumoto N, Sakai Y, Ohga S. Sonoda Y, et al. Among authors: wada y. Eur J Med Genet. 2024 Feb;67:104895. doi: 10.1016/j.ejmg.2023.104895. Epub 2023 Dec 7. Eur J Med Genet. 2024. PMID: 38070824 Free article. Review.
118 results