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The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
CCAAT/enhancer binding protein alpha (C/EBPalpha) in adipose tissue regulates genes in lipid and glucose metabolism and a genetic variation in C/EBPalpha is associated with serum levels of triglyceridesLouise E Olofsson, Marju Orho-Melander, Lena William-Olsson, et al.Journal of Renal Care|January 20, 2015
Continuing education: preparing patients to choose a renal replacement therapyTony Goovaerts, Corinne Bagnis Isnard, Carlo Crepaldi, et al.BMC Medicine|May 1, 2019
Elevated plasma copeptin levels identify the presence and severity of non-alcoholic fatty liver disease in obesityIlaria Barchetta, Sofia Enhörning, Flavia Agata Cimini, et al.Research and Practice in Thrombosis and Haemostasis|November 16, 2022
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort studyEric Manderstedt, Christina Lind-Halldén, Christer Halldén, et al.Cardiovascular Diabetology|October 3, 2025
Development and evaluation of a machine learning prediction model for short-term mortality in patients with diabetes or hyperglycemia at emergency department admissionPer Wändell, Marcelina Wierzbicka, Karolina Sigurdsson, et al.The Journal of Clinical Endocrinology and Metabolism|March 13, 2024
The Effects of Calorie Restriction and Bariatric Surgery on Circulating Proneurotensin LevelsMichael G Miskelly, Johan Berggren, Malin Svensson, et al.American Journal of Physiology. Endocrinology and Metabolism|October 4, 2023
Dual amylin and calcitonin receptor agonist treatment reduces biomarkers associated with kidney fibrosis in diabetic ratsSimone Anna Melander, Alexandra Louise Møller, Khaled Elhady Mohamed, et al.Thrombosis and Haemostasis|January 30, 2018
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis InhibitorTara M Stanne, Maja Olsson, Erik Lorentzen, et al.DNA Sequence : the Journal of DNA Sequencing and Mapping|July 27, 2007
Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in SwedesCristiano Fava, Martina Montagnana, Lena Rosberg, et al.Genes & Nutrition|November 18, 2021
Effect of AMY1 copy number variation and various doses of starch intake on glucose homeostasis: data from a cross-sectional observational study and a crossover meal studyMary Farrell, Stina Ramne, Phébée Gouinguenet, et al.Pageof 171