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Ole Hamberg

Researcher at University of Copenhagen

Publications -  14
Citations -  2187

Ole Hamberg is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Urea & Liver function. The author has an hindex of 8, co-authored 13 publications receiving 1783 citations.

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Nutritional risk screening (NRS 2002): a new method based on an analysis of controlled clinical trials.

TL;DR: The screening system appears to be able to distinguish between trials with a positive effect vs no effect, and it can therefore probably also identify patients who are likely to benefit from nutritional support.
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Effects of an increase in protein intake on hepatic efficacy for urea synthesis in healthy subjects and in patients with cirrhosis.

TL;DR: The study shows that an increase in protein intake selectively increases liver function with regard to disposal of amino nitrogen; the mechanism is qualitatively intact but quantitatively deficient in patients with cirrhosis of the liver, and does not seem to depend on glucagon.
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Effects of insulin and glucose on urea synthesis in normal man, independent of pancreatic hormone secretion

TL;DR: The inhibitory effect of insulin and glucose on hepatic amino- to urea-nitrogen conversion independent of endogenous insulin and glucagon secretion means that the hepatic component of the amino-N-sparing effect of glucose depends on hyperglycaemia but not on hyperinsulinaemia.
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Effects of budesonide and prednisolone on hepatic kinetics for urea synthesis.

TL;DR: Prednisolone administration led to increased levels of amino acids in blood and loss of N as urea, the latter in part due to a specific hepatic mechanism as shown by the increased FHNC, making treatment with budesonide superior to that of conventional glucocorticoids in this respect.
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Increased hepatic urea synthesis in patients with active inflammatory bowel disease.

TL;DR: The results show that the liver function related to conversion of amino-nitrogen to urea is increased in patients with active inflammatory bowel disease, and the accelerated hepatic amino- Nitrogen conversion contributes to the less efficient nitrogen economy in Patients with activeinflammatory bowel disease.