Results 231 to 240 of about 5,285,476 (282)
Some of the next articles are maybe not open access.
Lancet, The, 1977
18 454 men and 5471 women attending a screening centre had serum-bilirubin concentrations measured. 2.0% of men and 0.6% of women had concentrations of 25 micronmol/1 (1-5 MG/DL) or above. Both sexes showed skewed distributions for bilirubin concentration, but analysis of the data showed no evidence of bimodality for either sex.
A M Dawson, Alan Bailey
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18 454 men and 5471 women attending a screening centre had serum-bilirubin concentrations measured. 2.0% of men and 0.6% of women had concentrations of 25 micronmol/1 (1-5 MG/DL) or above. Both sexes showed skewed distributions for bilirubin concentration, but analysis of the data showed no evidence of bimodality for either sex.
A M Dawson, Alan Bailey
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GILBERT'S DISEASE: HAS IT EVER EXISTED?
Lancet, The, 1977W G Cooksley, L W Powell, G C Farrell
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A Diagnostic Test for "Gilbert's Disease."
Annals of Internal Medicine, 1963Excerpt Intravenously administered 1-131 iodipamide (R.I.I.) is rapidly concentrated in the normal human liver.
J. T. Galambos, J. R. McLaren
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Hepatic Uptake Defect in Patients with "Gilbert's Disease"
Archives of Internal Medicine, 1963Radioactive-iodide-labeled iodipamide (R.I.I.) is a simple, practical, and useful liver function test. In general it gives the same information that is obtained by sulfobromophthalein (SBP) retention studies. 1 Adequate collimation is of paramount importance when the hepatic uptake is measured after the intravenous injection of R.I.I. Method After an
J T, GALAMBOS, J R, McLAREN
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[Gilbert disease and isotretinoin].
Annales de dermatologie et de venereologie, 1998Because of the potential hepatotoxicity of retinoids, prescription of isotretinoin is always very carefully made in healthy subjects, and prohibited in case of concomitant hepatopathy. Gilbert's syndrome consists of chronic, mild, unconjugated hyperbilirubinemia. In this syndrome, isotretinoin has been reported twice to be perfectly tolerated, and once
F A, Le Gal, C, Pauwels
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[The heterogeneity of paracetamol metabolism in Gilbert's disease].
Gastroenterologia y hepatologia, 1999Gilbert's syndrome (GS) is a hereditary deficiency of bilirubin UDP-glucuronosyltransferase (UGT). The aim of this study was to analyze changes in the metabolism of paracetamol, which is primarily eliminated by liver glucuronidation, through urine concentrations of its four principal hepatic metabolites, in persons with GS.Thirty-two healthy volunteers
A, Esteban Rodríguez +1 more
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Celiac Disease in Association with Gilbert’s Syndrome
The Indian Journal of Pediatrics, 2018Ajay Kumar, Vyom Aggarwal
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Prolonged Newborn Jaundice and Gilbert's Disease
American Journal of Gastroenterology, 1999openaire +1 more source
Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population
Journal of Clinical and Experimental Hepatology, 2018Mithun Sharma
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