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139 results

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Page 1
Prognostic impact of left ventricular noncompaction in patients with Duchenne/Becker muscular dystrophy--prospective multicenter cohort study.
Kimura K, Takenaka K, Ebihara A, Uno K, Morita H, Nakajima T, Ozawa T, Aida I, Yonemochi Y, Higuchi S, Motoyoshi Y, Mikata T, Uchida I, Ishihara T, Komori T, Kitao R, Nagata T, Takeda S, Yatomi Y, Nagai R, Komuro I. Kimura K, et al. Among authors: motoyoshi y. Int J Cardiol. 2013 Oct 3;168(3):1900-4. doi: 10.1016/j.ijcard.2012.12.058. Epub 2013 Jan 17. Int J Cardiol. 2013. PMID: 23333368
Prognostic impact of venous thromboembolism in patients with Duchenne muscular dystrophy: Prospective multicenter 5-year cohort study.
Kimura K, Morita H, Daimon M, Kawata T, Nakao T, Lee SL, Hirokawa M, Ebihara A, Nakajima T, Ozawa T, Yonemochi Y, Aida I, Motoyoshi Y, Mikata T, Uchida I, Komori T, Kitao R, Nagata T, Takeda S, Komaki H, Segawa K, Takenaka K, Komuro I. Kimura K, et al. Among authors: motoyoshi y. Int J Cardiol. 2015 Jul 15;191:178-80. doi: 10.1016/j.ijcard.2015.04.244. Epub 2015 May 1. Int J Cardiol. 2015. PMID: 25965627 No abstract available.
Relationship of natriuretic peptide and transthoracic echocardiographic findings in 135 subjects with muscular dystrophy.
Kawakubo M, Funabashi N, Takahashi M, Sueishi M, Motoyoshi Y, Mikata T, Uchida I, Asakawa T, Takahashi R, Takamatsu M, Matsuoka Y, Minegishi M, Naga H, Yajima R, Kataoka A, Lee K, Komuro I. Kawakubo M, et al. Among authors: motoyoshi y. Int J Cardiol. 2010 Dec 3;145(3):506-14. doi: 10.1016/j.ijcard.2009.12.018. Epub 2010 Jan 12. Int J Cardiol. 2010. PMID: 20061036 No abstract available.
Tranilast for advanced heart failure in patients with muscular dystrophy: a single-arm, open-label, multicenter study.
Matsumura T, Hashimoto H, Sekimizu M, Saito AM, Motoyoshi Y, Nakamura A, Kuru S, Fukudome T, Segawa K, Takahashi T, Tamura T, Komori T, Watanabe C, Asakura M, Kimura K, Iwata Y. Matsumura T, et al. Among authors: motoyoshi y. Orphanet J Rare Dis. 2022 May 16;17(1):201. doi: 10.1186/s13023-022-02352-3. Orphanet J Rare Dis. 2022. PMID: 35578298 Free PMC article.
Unique tauopathy in Fukuyama-type congenital muscular dystrophy.
Saito Y, Motoyoshi Y, Kashima T, Izumiyama-Shimomura N, Toda T, Nakano I, Hasegawa M, Murayama S. Saito Y, et al. Among authors: motoyoshi y. J Neuropathol Exp Neurol. 2005 Dec;64(12):1118-26. doi: 10.1097/01.jnen.0000190069.10633.c2. J Neuropathol Exp Neurol. 2005. PMID: 16319722
139 results