Search Results - "Yamamoto, Shouhei"

The first case of adenine phosphoribosyltransferase deficiency with APRTQ0 (M1I) mutation in Japan by Ikeda, Hirokazu, Watanabe, Tsuneki, Fujimoto, Yoko, Yamamoto, Shouhei, Hosaki, Ichiro, Isoyama, Keiichi, Kawano, Shinya, Chiba, Masahiro

“…Adenine phosphoribosyltransferase (APRT) deficiency is an enzyme deficiency associated with purine metabolism, a hereditary disease that causes recurrent 2,…”
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The first case of adenine phosphoribosyltransferase deficiency with APRT Q0 (M1V) mutation in Japan by Ikeda, Hirokazu, Watanabe, Tsuneki, Fujimoto, Yoko, Yamamoto, Shouhei, Hosaki, Ichiro, Isoyama, Keiichi, Kawano, Shinya, Chiba, Masahiro

“…Adenine phosphoribosyltransferase (APRT) deficiency is an enzyme deficiency associated with purine metabolism, a hereditary disease that causes recurrent 2,…”
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Dramatic improvement in innominate artery compression syndrome with only postural changes in a bedridden elderly patient by Hamada, Noboru, Yamamoto, Shouhei, Kinoshita, Akinori, Saito, Eisuke, Yuzurio, Syouta, Habara, Risa, Suwaki, Toshimitsu

“…We present the case of a bedridden elderly patient who demonstrated dramatic improvement in innominate artery compression syndrome with postural changes alone…”
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Dramatic improvement in innominate artery compression syndrome with only postural changes in a bedridden elderly patient by Hamada, Noboru, Yamamoto, Shouhei, Kinoshita, Akinori, Saito, Eisuke, Yuzurio, Syouta, Habara, Risa, Suwaki, Toshimitsu

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