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4. No evidence of compensatory changes in energy balance, despite reductions in body weight and liver fat, during dapagliflozin treatment in type 2 diabetes mellitus: A randomized, double‐blind, placebo‐controlled, cross‐over trial (ENERGIZE)

6. sj-docx-5-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

7. sj-docx-9-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

8. sj-docx-15-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

9. sj-docx-4-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

10. sj-docx-2-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

11. sj-docx-3-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

12. sj-docx-6-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

13. sj-docx-7-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

14. sj-docx-8-dhj-10.1177_20552076231183552 - Supplemental material for Adherence to unsupervised exercise in sedentary individuals: A randomised feasibility trial of two mobile health interventions

18. In Reply

21. Mobile Health Biometrics to Enhance Exercise and Physical Activity Adherence in Type 2 Diabetes (MOTIVATE-T2D): protocol for a feasibility randomised controlled trial

23. A randomised, controlled, double blind study to assess mechanistic effects of combination therapy of dapagliflozin with exenatide QW versus dapagliflozin alone in obese patients with type 2 diabetes mellitus (RESILIENT): study protocol

24. Short-Term Physical Inactivity Induces Endothelial Dysfunction

30. Randomised, cOntrolled Multicentre trial of 26 weeks subcutaneous liraglutide (a glucagon-like peptide-1 receptor Agonist), with or without contiNuous positive airway pressure (CPAP), in patients with type 2 diabetes mellitus (T2DM) and obstructive sleep apnoEa (OSA) (ROMANCE): study protocol assessing the effects of weight loss on the apnea–hypnoea index (AHI)

32. Seven day remote ischaemic preconditioning improves endothelial function in patients with type 2 diabetes mellitus:a randomised pilot study

33. Physical Activity and Sedentary Time: Association with Metabolic Health and Liver Fat

34. Relationship Between Endothelial Function and the Eliciting Shear Stress Stimulus in Women: Changes Across the Lifespan Differ to Men

37. Untitled Reply

38. Letters To The Editor

40. Compensatory changes in energy balance during dapagliflozin treatment in type 2 diabetes mellitus: a randomised double-blind, placebo-controlled, cross-over trial (ENERGIZE)—study protocol

42. Dissociation between exercise-induced reduction in liver fat and changes in hepatic and peripheral glucose homoeostasis in obese patients with non-alcoholic fatty liver disease

43. External validation of the fatty liver index and lipid accumulation product indices, using 1H-magnetic resonance spectroscopy, to identify hepatic steatosis in healthy controls and obese, insulin-resistant individuals

46. Exercise training and artery function in humans: nonresponse and its relationship to cardiovascular risk factors

47. Ectopic lipid storage in non-alcoholic fatty liver disease is not mediated by impaired mitochondrial oxidative capacity in skeletal muscle

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