We are using cookies This website uses cookies in order to offer you the most relevant information. By browsing this website, you accept these cookies.
However, early initiation of chelation has also been associated with DFO toxicity.
2
Herein, we clarify the effect and mechanism of action of DFO on angiogenesis.
3
The DFO must be selected from the ranks of SAA pilots.
4
None of the patients who attained final height had signs of DFO bone toxicity.
5
UUO-induced expression of inflammatory cytokines and extracellular matrix proteins was abrogated by DFO treatment.
1
Reduction of iron load, achieved by regular desferrioxamine infusion, resulted in normalisation of the urinary enzyme levels.
2
In the presence of desferrioxamine, adriamycin semiquinone does not disappear in the presence of hydrogen peroxide at a detectable rate.
3
No significant changes in the degree of IRI or AR were observed in the groups treated with desferrioxamine or melatonin.
4
In our study, treatment with the antioxidants melatonin or desferrioxamine before reperfusion had no effects on IRI damage or on AR frequency or severity.
Usage of déferoxamine in inglés
1
Both NO inhibition and iron scavenging, using deferoxamine administration, reduced hydroxyl radical levels and neuronal cell death.
2
Likewise, depletion of iron by deferoxamine during induction of HO-1 by cobalt-protoporphyrin IX did not restore HCV replication.
3
DFE was 10 times more potent and more rapid in onset of effect than the clinically used iron chelator deferoxamine.
4
This increase was not significantly altered by SOD or deferoxamine, nor was it different from the mortality observed in air-exposed cells.
5
In patients previously exposed to aluminum, a deferoxamine test should be performed and a deferoxamine treatment started if the test is positive.
6
The ferric iron chelator deferoxamine prevented cell death and totally quenched the DMPO-R signal with a 40% decrease in the DMPO-OH signal.
7
These data indicate that iron overload may negatively affect CD4 Th1 development in mice with candidiasis, a function efficiently restored by therapy with deferoxamine.
8
Deferoxamine reduced the incidence of ventricular fibrillation to the same degree as ceruloplasmin but at concentrations much higher than those of ceruloplasmin.