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European Journal of Endocrinology|April 8, 2000
Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish familiesA Costa, M Bescós, G Velho, et al.
Diabetes & Metabolism|December 3, 2008
Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan populationY El Achhab, D Meyre, N Bouatia-Naji, et al.
American Journal of Human Genetics|January 1, 1997
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6M Delépine, F Pociot, C Habita, et al.
Geriatrics|June 12, 1999
Carotid occlusive disease: primary care of patients with or without symptomsJ R Eugene, M Abdallah, M Miglietta, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|April 5, 2007
Conjoined epigastric heteropagus twins: excision of a parasitic twin from the anterior abdominal wall of her siblingJ Hager, M Sanal, R Trawöger, et al.
Journal of the American Society for Mass Spectrometry|April 16, 2016
Preliminary Figures of Merit for Isotope Ratio Measurements: The Liquid Sampling-Atmospheric Pressure Glow Discharge Microplasma Ionization Source Coupled to an Orbitrap Mass AnalyzerEdward D Hoegg, Charles J Barinaga, George J Hager, et al.
Diabetes & Metabolism|January 27, 2005
Genetic study of the CD36 gene in a French diabetic populationF Leprêtre, K J Linton, C Lacquemant, et al.
International Journal of Obesity (2005)|October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French populationS Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Biochimica Et Biophysica Acta|July 2, 2014
Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetesP Perimenis, T Bouckenooghe, J Delplanque, 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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