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Blut|October 1, 1990
Congenital diserythropoietic anemia type I. Report on monozygotic twins with associated hemochromatosis and short statureT Facon, L Mannessier, P Lepelley, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1992
Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndromeR Medlej, J M Lobaccaro, P Berta, et al.
Neurology. Clinical Practice|November 16, 2022
Discordance Between Perceptions and Experience of Lumbar Puncture: A Prospective StudyYoshie Umemura, Baber Khan, Benjamin J Weill, et al.
Diabetologia|January 20, 2007
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjectsA Siddiq, M Gueorguiev, C Samson, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2002
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French CaucasiansJ Delplanque, F Vasseur, E Durand, et al.
Annals of Human Genetics|October 24, 2008
A genetic study of the ghrelin and growth hormone secretagogue receptor (GHSR) genes and statureM Gueorguiev, C Lecoeur, M Benzinou, 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.
Hormone Research in Paediatrics|May 11, 2010
Autoimmune polyendocrine syndrome type 1 in north-western France: AIRE gene mutation specificities and severe forms needing immunosuppressive therapiesE Proust-Lemoine, P Saugier-Véber, D Lefranc, et al.
Diabetes Care|July 8, 1998
Factors associated with glycemic control. A cross-sectional nationwide study in 2,579 French children with type 1 diabetes. The French Pediatric Diabetes GroupM Rosilio, J B Cotton, M C Wieliczko, et al.
The Journal of Pediatrics|February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathyJ L Michaud, E Héon, F Guilbert, et al.
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