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Diabetes, Obesity & Metabolism|November 21, 2013
Intensification of medication and glycaemic control among patients with type 2 diabetes - the ADVANCE trialS van Dieren, A P Kengne, J Chalmers, et al.The Journal of Nutrition, Health & Aging|February 23, 2007
IANA (International Academy on Nutrition and Aging) Expert Group: weight loss and Alzheimer's diseaseS Gillette Guyonnet, G Abellan Van Kan, E Alix, et al.Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.Journal of Hypertension. Supplement : Official Journal of the International Society of Hypertension|May 29, 2003
Effect of indapamide SR on microalbuminuria--the NESTOR study (Natrilix SR versus Enalapril Study in Type 2 diabetic hypertensives with micrOalbuminuRia)--rationale and protocol for the main trialM Marre, J Garcia Puig, F Kokot, et al.The Journal of Nutrition, Health & Aging|August 3, 2011
IAGG workshop: health promotion program on prevention of late onset dementiaS Andrieu, I Aboderin, J P Baeyens, et al.Presse Medicale (Paris, France : 1983)|November 23, 2005
[Consensus statement on severe dementia]B Vellas, S Gauthier, H Allain, et al.Revue Neurologique|October 26, 2005
[Consensus statement on severe dementia]B Vellas, S Gauthier, H Allain, et al.The Journal of Nutrition, Health & Aging|October 8, 2013
Promoting access to innovation for frail old persons. IAGG (International Association of Gerontology and Geriatrics), WHO (World Health Organization) and SFGG (Société Française de Gériatrie et de Gérontologie) Workshop--Athens January 20-21, 2012G Berrut, S Andrieu, I Araujo de Carvalho, et al.The Journal of Clinical Endocrinology and Metabolism|May 28, 2009
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytesM Laloi-Michelin, T Meas, C Ambonville, et al.Diabetologia|November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesA Albrechtsen, N Grarup, Y Li, et al.Pageof 22