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Department of Clinical Chemistry, Amsterdam Gastroenterology & Metabolism, Amsterdam UMC, University of Amsterdam, Endocrine Laboratory, Amsterdam, Netherlands
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vitamin D supplementation on the n-oxPTH concentrations in comparison to tPTH in a population with normal renal function. For this purpose, we measured n-oxPTH in the Styrian Hypertension Study, a vitamin D randomised controlled trial ( 14 ). In addition
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randomise interventions. Four of the test subjects received LPS during their first trial followed by placebo during their second trial and the other four test subjects received placebo first followed by LPS. During each trial, intravenous catheters were
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, EPN 2013/161 Uppsala, and the Medical Products Agency in Sweden and was pre-registered: EUDRA-CT 2013-000925-30. Study design The study was a double-blind, randomised, parallel-group clinical trial during which the participants were treated
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Morbid Obesity Centre, Department of Nutrition, Norwegian National Advisory Unit on Familial Hypercholesterolemia, Department of Gynecology, Institute of Clinical Medicine, Department of Endocrinology, Vestfold Hospital Trust, PO Box 2168, 3103 Tønsberg, Norway
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Morbid Obesity Centre, Department of Nutrition, Norwegian National Advisory Unit on Familial Hypercholesterolemia, Department of Gynecology, Institute of Clinical Medicine, Department of Endocrinology, Vestfold Hospital Trust, PO Box 2168, 3103 Tønsberg, Norway
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Morbid Obesity Centre, Department of Nutrition, Norwegian National Advisory Unit on Familial Hypercholesterolemia, Department of Gynecology, Institute of Clinical Medicine, Department of Endocrinology, Vestfold Hospital Trust, PO Box 2168, 3103 Tønsberg, Norway
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composition, gastrointestinal symptoms and hormonal characteristics of PCOS. Subjects and methods Study design, population and setting Parallel-group randomised controlled clinical trial (allocation ratio 1:1) of 18–40 years old treatment seeking morbidly
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Department of Cardiology, Department of Research, Institute of Clinical Studies, Clinical Research Unit, Department of Paediatrics, Department of Medicine, Department of Physiology and Nuclear Medicine, Institute of Clinical Medicine, Nephrology and Endocrinology
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Department of Cardiology, Department of Research, Institute of Clinical Studies, Clinical Research Unit, Department of Paediatrics, Department of Medicine, Department of Physiology and Nuclear Medicine, Institute of Clinical Medicine, Nephrology and Endocrinology
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Department of Cardiology, Department of Research, Institute of Clinical Studies, Clinical Research Unit, Department of Paediatrics, Department of Medicine, Department of Physiology and Nuclear Medicine, Institute of Clinical Medicine, Nephrology and Endocrinology
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relationship between 25(OH)D, risk of CVD (measured as carotid IMT, carotid artery DC and YEM) and bone health (measured as BMD and trabecular bone score (TBS)) in a Danish cohort of patients with T2D participating in a randomised clinical trial (The Copenhagen
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( 8 , 9 , 10 , 11 , 12 , 13 ). A multitarget TKI surufatinib has also showed promising efficacy in the Chinese population, which requires further confirmation in large clinical trials of other population ( 14 , 15 ). However, there is still an
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be of value in the clinical setting. In addition, the only randomised placebo-controlled trial in this review with the maximal points for methodology, found no effect of vitamin D supplementation (daily oral 800 IU vitamin D3) on the physical
INSERM U1018, Université Paris Sud, Centre for Research in Epidemiology and Population Health, Hôpital Paul Brousse, Bât 15/16, 16 Avenue Paul Vaillant Couturier, 94807 Paris, Villejuif Cedex, France
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been inconclusive (12) . Recent randomised controlled trials (RCTs) show that intensive glycaemic control does not have beneficial effects on the rate of cognitive decline (13, 14, 15, 16) . The increased frequency of hypoglycaemia in patients treated
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glycaemic control in patients hospitalised in a mixed medical and surgical intensive care unit: a randomised clinical trial . Critical Care 2008 12 R120 . ( https://doi.org/10.1186/cc7017 ) 36 Brunkhorst FM Engel C Bloos F Meier-Hellmann A Ragaller
Department of Medicine (Austin Health), University of Melbourne, Heidelberg, Victoria, Australia
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Department of Medicine (Austin Health), University of Melbourne, Heidelberg, Victoria, Australia
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Department of Medicine (Austin Health), University of Melbourne, Heidelberg, Victoria, Australia
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( 8 ). Pre-clinical data demonstrates modulation of the γ-aminobutyric acid type A (GABA-A) receptor, and micronised progesterone treatment has been found to reduce sleep onset latency and to improve self-reported sleep outcomes in randomised