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1 evaluated the influence of polymerization of diaspirin alpha-alpha cross-linked Hb (alphaalpha-DBBF-H
2 aortic endothelial cells were incubated with diaspirin cross-linked hemoglobin (DBBF-Hb), developed a
4 ted with 0.9% saline (group 1, 90 mL/ kg) or diaspirin cross-linked hemoglobin (group 2, 15 mL/kg) fr
5 nd hematologic analyses were measured before diaspirin cross-linked hemoglobin administration and at
10 fter pulmonary contusion, resuscitation with diaspirin cross-linked hemoglobin led to pulmonary hyper
14 re no serious adverse events associated with diaspirin cross-linked hemoglobin solution infusion.
15 entrations was observed in 12 subjects after diaspirin cross-linked hemoglobin solution infusion.
16 r control infusion and in six subjects after diaspirin cross-linked hemoglobin solution infusion; no
18 nd toe temperature were measured to evaluate diaspirin cross-linked hemoglobin solution's pharmacodyn
21 significantly after infusion of 100 mg/kg of diaspirin cross-linked hemoglobin solution; the isoenzym
28 endothelin in the cardiovascular actions of diaspirin crosslinked hemoglobin (modified) and (unmodif
29 odynamic and regional circulatory effects of diaspirin crosslinked hemoglobin and stroma reduced hemo
32 significantly increased after treatment with diaspirin crosslinked hemoglobin or stroma reduced hemog
35 and total peripheral vascular resistance by diaspirin crosslinked hemoglobin were significantly bloc
36 blood flow to the heart, spleen, and skin by diaspirin crosslinked hemoglobin were significantly bloc
37 fied, highly purified, and heat pasteurized (diaspirin crosslinked) and unmodified (stroma reduced) h
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