Search Results - Tsurusaki, Yoshiyuki

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  1. 1
    Synthesis and properties of superconductors prepared from ethylenediaminetetraacetic acid (EDTA)-ethylenediamine (ED) polyamide YBC chelate

    Synthesis and properties of superconductors prepared from ethylenediaminetetraacetic acid (EDTA)-ethylenediamine (ED) polyamide YBC chelate by Maeda, Shigeru, Tsurusaki, Yoshiyuki, Tachiyama, Yoshiyuki, Naka, Kensuke, Ohki, Akira, Ohgushi, Tetsuya, Takeshita, Toshio

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  2. 2
    Impact of Metformin on the Severity and Outcomes of Acute Ischemic Stroke in Patients with Type 2 Diabetes Mellitus

    Impact of Metformin on the Severity and Outcomes of Acute Ischemic Stroke in Patients with Type 2 Diabetes Mellitus by Mima, Yohei, MD, PhD, Kuwashiro, Takahiro, MD, PhD, Yasaka, Masahiro, MD, PhD, Tsurusaki, Yuichiro, MD, Nakamura, Asako, MD, PhD, Wakugawa, Yoshiyuki, MD, PhD, Okada, Yasushi, MD, PhD

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  3. 3
    Magnetic resonance imaging‐based risk factors of hepatocellular carcinoma after direct‐acting antiviral therapy: A multicenter observational study

    Magnetic resonance imaging‐based risk factors of hepatocellular carcinoma after direct‐acting antiviral therapy: A multicenter observational study by Ichikawa, Shintaro, Motosugi, Utaroh, Sawai, Yoshiyuki, Ishida, Hisashi, Imai, Yasuharu, Kozaka, Kazuto, Tsurusaki, Masakatsu, Sofue, Keitaro, Murakami, Takamichi, Kawai, Nobuyuki, Matsuo, Masayuki, Fukukura, Yoshihiko, Mawatari, Seiichi, Shimizu, Tatsuya, Morisaka, Hiroyuki, Inoue, Taisuke, Goshima, Satoshi

    Published in Hepatology research
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  4. 4
    Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation

    Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation by Doi, Hiroshi, Yoshida, Kunihiro, Yasuda, Takao, Fukuda, Mitsunori, Fukuda, Yoko, Morita, Hiroshi, Ikeda, Shu-ichi, Kato, Rumiko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Sakai, Haruya, Miyatake, Satoko, Shiina, Masaaki, Nukina, Nobuyuki, Koyano, Shigeru, Tsuji, Shoji, Kuroiwa, Yoshiyuki, Matsumoto, Naomichi

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  5. 5
    A novel WTX mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma

    A novel WTX mutation in a female patient with osteopathia striata with cranial sclerosis and hepatoblastoma by Fujita, Atsushi, Ochi, Nobuhiko, Fujimaki, Hidehiko, Muramatsu, Hideki, Takahashi, Yoshiyuki, Natsume, Jun, Kojima, Seiji, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Matsumoto, Naomichi, Miyake, Noriko

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  6. 6
    A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy

    A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy by Higashiyama, Yuichi, Doi, Hiroshi, Wakabayashi, Masatoshi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ohba, Chihiro, Fukai, Ryoko, Miyatake, Satoko, Joki, Hideto, Koyano, Shigeru, Suzuki, Yume, Tanaka, Fumiaki, Kuroiwa, Yoshiyuki, Matsumoto, Naomichi

    Published in Movement disorders
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  7. 7
    Increase in the Size of an Intracardiac Thrombus during Dabigatran Therapy (110 mg b.i.d.) in an Acute Cardioembolic Stroke Patient

    Increase in the Size of an Intracardiac Thrombus during Dabigatran Therapy (110 mg b.i.d.) in an Acute Cardioembolic Stroke Patient by Tabata, Emi, Yasaka, Masahiro, Wakugawa, Yoshiyuki, Komori, Motohiro, Mori, Kohta, Tsurusaki, Yuichiro, Kokuba, Kazuhito, Sambongi, Yoshiki, Maeda, Koichiro, Okada, Yasushi

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  8. 8
    A novel SCARB 2 mutation causing late‐onset progressive myoclonus epilepsy

    A novel SCARB 2 mutation causing late‐onset progressive myoclonus epilepsy by Higashiyama, Yuichi, Doi, Hiroshi, Wakabayashi, Masatoshi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ohba, Chihiro, Fukai, Ryoko, Miyatake, Satoko, Joki, Hideto, Koyano, Shigeru, Suzuki, Yume, Tanaka, Fumiaki, Kuroiwa, Yoshiyuki, Matsumoto, Naomichi

    Published in Movement disorders
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  9. 9
    A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy

    A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy by Higashiyama, Yuichi, Doi, Hiroshi, Wakabayashi, Masatoshi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ohba, Chihiro, Fukai, Ryoko, Miyatake, Satoko, Joki, Hideto, Koyano, Shigeru, Suzuki, Yume, Tanaka, Fumiaki, Kuroiwa, Yoshiyuki, Matsumoto, Naomichi

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