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1 ated the relation between VAS and underlying hypervitaminosis A assessed by retinol isotope dilution
6 population and could avoid the potential for hypervitaminosis A that was observed with the use of pre
7 ders such as obesity and hypoparathyroidism, hypervitaminosis A, tetracycline use and thyroid replace
12 of total serum vitamin A indicate potential hypervitaminosis, but this cutoff was derived from small
13 uption of the Klotho gene in mice results in hypervitaminosis D and a syndrome resembling accelerated
14 n of Fgf-23 in mice (Fgf-23(-/-)) results in hypervitaminosis D, abnormal mineral metabolism, and red