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International Journal of Obesity (2005)|September 27, 2017
Genetic predisposition to adiposity is associated with increased objectively assessed sedentary time in young childrenT M Schnurr, A Viitasalo, A-M Eloranta, et al.
Diabetologia|January 7, 2010
The effects of aerobic exercise on metabolic risk, insulin sensitivity and intrahepatic lipid in healthy older people from the Hertfordshire Cohort Study: a randomised controlled trialF M Finucane, S J Sharp, L R Purslow, et al.
BMC Endocrine Disorders|June 24, 2009
Randomized controlled trial of the efficacy of aerobic exercise in reducing metabolic risk in healthy older people: The Hertfordshire Physical Activity TrialFrancis M Finucane, Jessica Horton, Lisa R Purslow, et al.
Molecular Genetics and Metabolism|July 17, 2012
Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland--experience and development of a routine program for expanded newborn screeningAllan Meldgaard Lund, David Michael Hougaard, Henrik Simonsen, et al.
Diabetologia|January 11, 2020
A pragmatic and scalable strategy using mobile technology to promote sustained lifestyle changes to prevent type 2 diabetes in India and the UK: a randomised controlled trialArun Nanditha, Hazel Thomson, Priscilla Susairaj, et al.
Nucleic Acids Research|June 10, 2022
Topoisomerase 1 inhibits MYC promoter activity by inducing G-quadruplex formationJosephine Geertsen Keller, Kirstine Mejlstrup Hymøller, Maria Eriksen Thorsager, et al.
Public Health in Practice (Oxford, England)|June 3, 2024
Impact of a nationwide school policy on body mass index in Danish school children: An interrupted time series analysisNatascha H Pedersen, Anders Grøntved, Niels C Møller, et al.
Open Heart|November 2, 2019
Rationale for the ASSAIL-MI-trial: a randomised controlled trial designed to assess the effect of tocilizumab on myocardial salvage in patients with acute ST-elevation myocardial infarction (STEMI)Anne Kristine Anstensrud, Sindre Woxholt, Kapil Sharma, et al.
Human Genetics|June 5, 2008
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular levelChristina B Pedersen, Steen Kølvraa, Agnete Kølvraa, et al.
Brain : a Journal of Neurology|June 23, 2007
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Simon E Olpin, Brage S Andresen, et al.
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