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A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction.
Nakajima R, Sekiya M, Furuta Y, Miyamoto T, Sato M, Fukuda K, Hattori K, Suehara Y, Sakata-Yanagimoto M, Chiba S, Okajima Y, Matsuzaka T, Takase S, Takanashi M, Okazaki H, Takashima Y, Yuhara M, Mitani Y, Matsumoto N, Murayama Y, Ohyama Osawa M, Ohuchi N, Yamazaki D, Mori S, Sugano Y, Osaki Y, Iwasaki H, Suzuki H, Shimano H. Nakajima R, et al. Among authors: yuhara m. Endocrinol Diabetes Metab Case Rep. 2022 Dec 1;2022:22-0368. doi: 10.1530/EDM-22-0368. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 36571472 Free PMC article.
A case of early-onset diabetes with impaired insulin secretion carrying a PAX6 gene Gln135* mutation.
Sekiya M, Yuhara M, Murayama Y, Ohyama Osawa M, Nakajima R, Ohuchi N, Matsumoto N, Yamazaki D, Mori S, Matsuda T, Sugano Y, Osaki Y, Iwasaki H, Suzuki H, Shimano H. Sekiya M, et al. Among authors: yuhara m. Endocrinol Diabetes Metab Case Rep. 2022 Aug 1;2022:22-0271. doi: 10.1530/EDM-22-0271. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 35979842 Free PMC article.
31 results