Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kenn Dornonville de la Cour"'
Autor:
Frauke Rudolf, Mads Damkjær, Suzanne Lunding, Kenn Dornonville de la Cour, Alyssa Young, Tim Brooks, Tom Sesay, Alex P. Salam, Sharmistha Mishra, Merete Storgaard
Publikováno v:
Emerging Infectious Diseases, Vol 23, Iss 4, Pp 597-600 (2017)
Case-fatality rates in Ebola treatment centers (ETCs) varied widely during the Ebola virus disease (EVD) outbreak in West Africa. We assessed the influence of referral pathway on ETC case-fatality rates with a retrospective cohort of 126 patients tre
Externí odkaz:
https://doaj.org/article/bbd9f426710841b7b85f64d36faf33d8
Autor:
Ida Kuhlmann, Kim Brøsen, Kenn Dornonville de la Cour, Troels K Bergmann, Mette Marie Hougaard Christensen, Tore Bjerregaard Stage, Stine Thorhauge Zwisler, Per Damkier, Anders Gadegaard Jensen, Rasmus Hjelmar Petersen, Flemming Nielsen, Morten Overgaard
Publikováno v:
Kuhlmann, I, Petersen, R H, Overgaard, M, Dornonville de la Cour, K, Zwisler, S, Stage, T B, Christensen, M M H, Bergmann, T K, Damkier, P, Jensen, A G, Nielsen, F & Brøsen, K 2022, ' No significant influence of OCT1 genotypes on the pharmacokinetics of morphine in adult surgical patients ', Basic & Clinical Pharmacology & Toxicology, vol. 130, no. 1, pp. 93-102 . https://doi.org/10.1111/bcpt.13667
We investigated the impact of genetic variants in OCT1 (SLC22A1) on morphine, morphine-3-glucuronide (M3G) and morphine-6-glucuronide (M6G) pharmacokinetics in adult patients scheduled for major surgery. Blood samples were taken before and 5, 10, 15,
Autor:
Kenn, Dornonville de la Cour
Publikováno v:
Ugeskrift for laeger. 175(39)
Central pontin myelinolysis has since the 1970s been correlated with hyponatraemia. A 56-year-old woman was admitted to hospital after a few days of diminished capacity and acute disorientation and respiratory distress. Initially, her alcohol overcon
Autor:
Kenn, Dornonville de la Cour
Publikováno v:
Ugeskrift for laeger. 175(39)
Initially central pontin myelinolysis was associated with alcoholism and later with hyponatraemia and particularly the correction rate. The diagnosis is made by characteristic symptoms and cerebral MRI with areas of hyperintensity on T2-weighted imag