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Annales De Cardiologie Et D'Angeiologie|February 7, 2006
[Main issues and contributions of the evaluation of health care networks]J Antras-Ferry, A L Laprérie, E Gravoueille, et al.
Journal of Diabetes and Its Complications|December 13, 2000
Epidemiological analysis of patients with Type 2 diabetes in FranceA Grimaldi, V Grangé, H Allannic, 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.
Diabetes & Metabolism|June 1, 1997
Multicentre evaluation of the DCA 2000 system for measuring glycated haemoglobin. DCA 2000 Study GroupB Guerci, D Durain, H Leblanc, et al.
Diabetes|June 1, 1997
Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairsN Vionnet, E H Hani, S Lesage, et al.
Orphanet Journal of Rare Diseases|February 23, 2022
Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM studyD Pougheon Bertrand, A Fanchini, P Lombrail, et al.
Annals of Physical and Rehabilitation Medicine|April 26, 2011
Multiple sclerosis and access to healthcare in the Pays de la Loire region: preliminary study based on 130 self-applied double questionnairesM Le Fort, S Wiertlewski, I Bernard, et al.
Orphanet Journal of Rare Diseases|February 22, 2023
A conceptual framework to develop a patient-reported experience questionnaire on the cystic fibrosis journey in France: the ExPaParM collaborative studyD Pougheon Bertrand, A Fanchini, P Lombrail, et al.
The Journal of Clinical Investigation|April 1, 1997
Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie Diabetique (GENEDIAB) study groupM Marre, X Jeunemaitre, Y Gallois, et al.
Human Molecular Genetics|December 6, 2001
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27S Francke, M Manraj, C Lacquemant, et al.
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