S
Soroku Nishiyama
Researcher at Kumamoto University
Publications - 37
Citations - 1096
Soroku Nishiyama is an academic researcher from Kumamoto University. The author has contributed to research in topics: Zinc deficiency & Parathyroid hormone. The author has an hindex of 19, co-authored 37 publications receiving 1053 citations.
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Journal ArticleDOI
Transient hypothyroidism or persistent hyperthyrotropinemia in neonates born to mothers with excessive iodine intake.
Soroku Nishiyama,Tomohiro Mikeda,Toshihisa Okada,Kimitoshi Nakamura,Tomio Kotani,Akira Hishinuma +5 more
TL;DR: It is proposed that hyperthyrotropinemia related to excessive iodine ingestion by the mother during pregnancy in some cases may not be transient, and consumption of iodine by the postnatal child and susceptibility to the inhibitory effect of iodine may contribute in part to the persistent hyperthyroidism.
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Mild to moderate zinc deficiency in short children: Effect of zinc supplementation on linear growth velocity
Toshiro Nakamura,Soroku Nishiyama,Yoshiko Futagoishi-Suginohara,Ichiro Matsuda,Akimasa Higashi +4 more
TL;DR: It is concluded that zinc supplementation is effective for inducing growth in short children with zinc deficiency, and that body zinc clearance tests facilitate detection of marginal zinc deficiency.
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Studies on the lipid and apolipoprotein compositions of two species of apoA-I-containing lipoproteins in normolipidemic males and females.
TL;DR: Of considerable significance is the finding that the ratio of cholesteryl ester to total cholesterol in LpA-I was significantly lower than that in L pA- I/A-II in both males and females, which might suggest that Lp a-I could be a carrier of free cholesterol.
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Differences in basal and postexercise osteocalcin levels in athletic and nonathletic humans
TL;DR: It is speculated that athletic subjects have a higher turnover of bone status compared with nonathletic subjects.
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Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan
Akira Hishinuma,Shuji Fukata,Soroku Nishiyama,Yoshikazu Nishi,Masamichi Oh-Ishi,Yoshiharu Murata,Yoshihide Ohyama,Nobuo Matsuura,Kikuo Kasai,Shohei Harada,Sachiko Kitanaka,Junta Takamatsu,Kohji Kiwaki,Hidemi Ohye,Takashi Uruno,Chisato Tomoda,Toshihiro Tajima,Kanji Kuma,Akira Miyauchi,Tamio Ieiri +19 more
TL;DR: The occurrence of Tg mutation within the general Japanese population is one in 67,000, and the result suggests that Tg mutations may provide a genetic basis for the cause of familial euthyroid goiter.