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Page 1
Achilles tendon thickness is associated with coronary lesion severity in acute coronary syndrome patients without familial hypercholesterolemia.
Fujiwara R, Yahiro R, Horio T, Miyauchi M, Yoshimura R, Matsuoka Y, Yokouchi G, Sakamoto Y, Matsumoto N, Fukuda K, Izumiya Y, Yoshiyama M, Fujimoto K, Kasayuki N. Fujiwara R, et al. Among authors: matsumoto n. J Cardiol. 2022 Feb;79(2):311-317. doi: 10.1016/j.jjcc.2021.09.021. Epub 2021 Oct 15. J Cardiol. 2022. PMID: 34657775 Free article.
Renoprotective effect of chronic treatment with sodium-glucose cotransporter 2 inhibitors and its associated factors in Japanese patients with chronic heart failure and diabetes.
Yokouchi G, Horio T, Matsumoto N, Fukuda K, Yoshimura R, Fujiwara R, Matsuoka Y, Sakamoto Y, Iwashima Y, Oshiro Y, Fujimoto K, Kasayuki N. Yokouchi G, et al. Among authors: matsumoto n. Int J Cardiol Heart Vasc. 2022 Nov 26;43:101152. doi: 10.1016/j.ijcha.2022.101152. eCollection 2022 Dec. Int J Cardiol Heart Vasc. 2022. PMID: 36457725 Free PMC article.
Alogliptin after acute coronary syndrome in patients with type 2 diabetes.
White WB, Cannon CP, Heller SR, Nissen SE, Bergenstal RM, Bakris GL, Perez AT, Fleck PR, Mehta CR, Kupfer S, Wilson C, Cushman WC, Zannad F; EXAMINE Investigators. White WB, et al. N Engl J Med. 2013 Oct 3;369(14):1327-35. doi: 10.1056/NEJMoa1305889. Epub 2013 Sep 2. N Engl J Med. 2013. PMID: 23992602 Free article. Clinical Trial.
Clinical and genetic spectrum of patients with IRF2BPL syndrome.
Iwama K, Kato M, Uchiyama Y, Sakamoto M, Miyamoto R, Izumi Y, Ohashi K, Hattori A, Yoshida N, Azuma Y, Watanabe A, Ikeda C, Shimizu-Motohashi Y, Kusabiraki S, Nakagawa E, Sasaki M, Sugai K, Ohori S, Tsuchida N, Hamanaka K, Koshimizu E, Fujita A, Nakashima M, Miyatake S, Sengoku T, Ogata K, Saitoh S, Saitsu H, Ito S, Mizuguchi T, Matsumoto N. Iwama K, et al. Among authors: matsumoto n. J Hum Genet. 2025 Jan 22. doi: 10.1038/s10038-025-01316-2. Online ahead of print. J Hum Genet. 2025. PMID: 39843638
KNTC1 introduces segmental heterogeneity to mitochondria.
Tsukamura A, Ariyama H, Hayashi N, Miyatake S, Okado S, Sultana S, Terakado I, Yamamoto T, Yamanaka S, Fujii S, Hamanoue H, Asano R, Mizushima T, Matsumoto N, Maruo Y, Mori M. Tsukamura A, et al. Among authors: matsumoto n. Dis Model Mech. 2025 Jan 20:dmm.052063. doi: 10.1242/dmm.052063. Online ahead of print. Dis Model Mech. 2025. PMID: 39829138 Free article.
Triple mosaic variants of PURA in a patient with multiple congenital anomalies.
Fujita A, Suenaga Y, Takeshita E, Takahashi Y, Suzuki Y, Ohori S, Tsuchida N, Uchiyama Y, Koshimizu E, Miyatake S, Mizuguchi T, Matsumoto N. Fujita A, et al. Among authors: matsumoto n. J Hum Genet. 2025 Jan 14. doi: 10.1038/s10038-024-01315-9. Online ahead of print. J Hum Genet. 2025. PMID: 39809889
3,354 results