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International Angiology : a Journal of the International Union of Angiology|October 7, 2010
Clinical trials needed to evaluate compression therapy in breast cancer related lymphedema (BCRL). Proposals from an expert groupH Partsch, N Stout, I Forner-Cordero, et al.
The Journal of Clinical Investigation|March 1, 1994
Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutationsM M Byrne, J Sturis, K Clément, et al.
Clinical Genetics|June 21, 2008
Cathepsin S genotypes are associated with Apo-A1 and HDL-cholesterol in lean and obese French populationsN Spielmann, D M Mutch, F Rousseau, et al.
Obesity Surgery|March 5, 2021
Decision Tree for the Performance of Intraoperative Liver Biopsy During Bariatric SurgerySandrine Barbois, N Stürm, J Aron-Wisnewsky, et al.
Pediatric Obesity|June 2, 2012
Relevance of increased serum cystatin C to vascular alterations in obese childrenB Dubern, J C Lafarge, S Fellahi, et al.
The New England Journal of Medicine|August 10, 1995
Genetic variation in the beta 3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesityK Clément, C Vaisse, B S Manning, et al.
Journal Des Maladies Vasculaires|January 15, 2013
[Quality standards for ultrasonographic assessment of peripheral vascular malformations and vascular tumors. Report of the French Society for Vascular Medicine]J-P Laroche, F Becker, A Khau-Van-Kien, et al.
International Journal of Obesity (2005)|July 7, 2011
Assessment of epicardial fat volume and myocardial triglyceride content in severely obese subjects: relationship to metabolic profile, cardiac function and visceral fatB Gaborit, F Kober, A Jacquier, et al.
International Journal of Obesity (2005)|March 11, 2017
Serum lipidomics reveals early differential effects of gastric bypass compared with banding on phospholipids and sphingolipids independent of differences in weight lossB D Kayser, M Lhomme, M C Dao, et al.
Diabetes|April 1, 1996
Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutationG Velho, M M Byrne, K Clément, et al.
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