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MAMLD1 (CXorf6): a new gene for hypospadias.
Ogata T, Wada Y, Fukami M. Ogata T, et al. Among authors: wada y. Sex Dev. 2008;2(4-5):244-50. doi: 10.1159/000152040. Epub 2008 Nov 5. Sex Dev. 2008. PMID: 18987498 Review.
Clinical characteristics of adolescent cases with Type A insulin resistance syndrome caused by heterozygous mutations in the β-subunit of the insulin receptor (INSR) gene.
Takasawa K, Tsuji-Hosokawa A, Takishima S, Wada Y, Nagasaki K, Dateki S, Numakura C, Hijikata A, Shirai T, Kashimada K, Morio T. Takasawa K, et al. Among authors: wada y. J Diabetes. 2019 Jan;11(1):46-54. doi: 10.1111/1753-0407.12797. Epub 2018 Jul 4. J Diabetes. 2019. PMID: 29877041
Lactulose: A treatment for hyperammonemia in a lysinuric protein-intolerant patient with dynamic blood amino acid concentrations.
Kakisaka K, Sato T, Wada Y, Ito A, Eto H, Abe H, Kanazawa J, Yusa K, Kooka Y, Endo K, Yoshida Y, Oikawa T, Kuroda H, Miyasaka A, Akasaka M, Matsumoto T. Kakisaka K, et al. Among authors: wada y. Mol Genet Metab Rep. 2022 Jul 15;32:100898. doi: 10.1016/j.ymgmr.2022.100898. eCollection 2022 Sep. Mol Genet Metab Rep. 2022. PMID: 35865266 Free PMC article. No abstract available.
Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan.
Mikami-Saito Y, Wada Y, Arai-Ichinoi N, Nakajima Y, Suzuki-Ajihara S, Murayama K, Tanaka T, Numakura C, Hamazaki T, Igarashi N, Esaki H, Kagawa R, Kono T, Sawada T, Sawada T, Nyuzuki H, Hirai H, Fumoto S, Matsuda J, Matsunaga A, Maruyama S, Yamaguchi K, Yoshino M, Totsune E, Kikuchi A, Ohura T, Kure S. Mikami-Saito Y, et al. Among authors: wada y. Genet Med. 2024 May 16:101165. doi: 10.1016/j.gim.2024.101165. Online ahead of print. Genet Med. 2024. PMID: 38762772 Free article.
3,657 results