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Page 1
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: ogata k. J Hum Genet. 2025 Jan 22. doi: 10.1038/s10038-025-01316-2. Online ahead of print. J Hum Genet. 2025. PMID: 39843638
Comparative Outcomes of Supera Interwoven Nitinol Versus Eluvia Fluoropolymer-Based Drug-Eluting Stents for the Treatment of Severely Calcified Femoropopliteal Artery Lesions: Results of the ELDORADO Study.
Yanagiuchi T, Tokuda T, Yoshioka N, Kojima S, Tanaka A, Takei T, Ogata K, Yamaguchi K, Nakama T, Yokoi H; LEADers PAD investigators. Yanagiuchi T, et al. Among authors: ogata k. Catheter Cardiovasc Interv. 2025 Jan 8. doi: 10.1002/ccd.31409. Online ahead of print. Catheter Cardiovasc Interv. 2025. PMID: 39780368
Receptor-independent regulation of Gα13 by alpha-1-antitrypsin C-terminal peptides.
Park Y, Matsumoto S, Ogata K, Ma B, Kanada R, Isaka Y, Arichi N, Liang X, Maki R, Kozasa T, Okuno Y, Ohno H, Ishihama Y, Toyoshima F. Park Y, et al. Among authors: ogata k. J Biol Chem. 2024 Dec 25:108136. doi: 10.1016/j.jbc.2024.108136. Online ahead of print. J Biol Chem. 2024. PMID: 39730062 Free article.
Prognostic Factors Associated with 2-year Mortality in Patients with Intermittent Claudication Treated with Endovascular Therapy for Femoropopliteal Lesions: Results from the Multicenter PROCYON Study.
Takei T, Tokuda T, Yoshioka N, Ogata K, Tanaka A, Kojima S, Yamaguchi K, Yanagiuchi T, Nakama T; LEADers PAD (peripheral artery disease) investigators. Takei T, et al. Among authors: ogata k. J Atheroscler Thromb. 2024 Dec 25. doi: 10.5551/jat.65379. Online ahead of print. J Atheroscler Thromb. 2024. PMID: 39721706 Free article.
Clinical Characteristics of Patients With Becker Muscular Dystrophy Having Pathogenic Microvariants or Duplications.
Nakamura A, Matsumura T, Ogata K, Mori-Yoshimura M, Takeshita E, Kimura K, Arahata H, Takeshima Y, Takahashi T, Ishigaki K, Awano H, Sugie K, Fujii T, Oi H, Komaki H. Nakamura A, et al. Among authors: ogata k. Neurol Genet. 2024 Dec 17;11(1):e200215. doi: 10.1212/NXG.0000000000200215. eCollection 2025 Feb. Neurol Genet. 2024. PMID: 39712290 Free PMC article.
1,762 results