琉球大学 · 医学部 · 助教

研究关键词orofaciodigital syndrome type XVI・SMC1A mutation・Saul-Wilson syndrome・intractable epilepsy・skeletal dysplasia・rare disease case reports

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• Additional findings of tibial dysplasia in a male with orofaciodigital syndrome type XVI.2022 · Chinen Y, Nakamura S, Yanagi K, Kaneshi T, Goya H, Yoshida T, Satou K, Kaname T, Naritomi K, Nakanishi K
• A novel nonsense SMC1A mutation in a patient with intractable epilepsy and cardiac malformation.2019 · Chinen Y, Nakamura S, Kaneshi T, Nakayashiro M, Yanagi K, Kaname T, Naritomi K, Nakanishi K
• Progressive hip joint subluxation in Saul-Wilson syndrome.2015 · Chinen Y, Kaneshi T, Kamiya T, Hata K, Nishimura G, Kaname T
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