Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
BMC Geriatrics|October 17, 2019
The impact of an orthogeriatric intervention in patients with fragility fractures: a cohort studyCharlotte Abrahamsen, Birgitte Nørgaard, Eva Draborg, et al.
Ugeskrift for Laeger|October 9, 2014
[The complex clinical presentation of hereditary mitochondrial diseases]Anja Lisbeth Frederiksen, Morten Frost Nielsen, Knud Yderstræde, et al.
Ugeskrift for Laeger|October 9, 2014
[Diabetes and hearing impairment due to mitochondrial mutation]Jens-Jacob Lauterlein, Inger Olsen, Knud Yderstræde, et al.
Diabetes, Obesity & Metabolism|February 18, 2026
Real-world persistence and dose titration of GLP-1 receptor agonists in type 2 diabetes: A UK population-based cohort study by obesity and cardiovascular disease statusFranziska S Ulrich, Nicola Napoli, Morten Frost Nielsen, et al.
Diabetes, Obesity & Metabolism|February 25, 2026
Real-world treatment trajectories preceding GLP-1 receptor agonist initiation in type 2 diabetes: A descriptive UK population-based cohort study on adherence to national clinical guidelinesFranziska S Ulrich, Morten Frost Nielsen, Nicola Napoli, et al.
The Lancet Regional Health. Europe|June 15, 2026
Comparative Effectiveness and Safety of Once-Weekly Injectable Semaglutide Versus Dulaglutide in Individuals with Type 2 Diabetes Managed in UK Primary Care: A Population-Based Cohort StudyFranziska S Ulrich, Morten Frost Nielsen, Nicola Napoli, et al.
European Journal of Endocrinology|June 8, 2013
Autosomal dominant osteopetrosis revisited: lessons from recent studiesJens Bollerslev, Kim Henriksen, Morten Frost Nielsen, et al.
Biochimica Et Biophysica Acta|December 19, 2015
Normal hematopoiesis and lack of β-catenin activation in osteoblasts of patients and mice harboring Lrp5 gain-of-function mutationsMarta Galán-Díez, Adiba Isa, Marco Ponzetti, et al.
Genes|June 26, 2026
Differential DNA Methylation of the Serotonin Receptor Signaling and Glutamatergic Synapse Pathways in Adult Twins Born PretermCarl Peter Vittrup Rasmussen, Marianne Nygaard, Morten Frost Nielsen, et al.
Clinical Case Reports|October 21, 2016
Asymptomatic parental mosaicism for osteogenesis imperfecta associated with a new splice site mutation in COL1A2Anja Lisbeth Frederiksen, Morten Duno, Iben B G Johnsen, et al.
Pageof 2