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Page 1
Lipoatrophic diabetes: genetic exclusion of the insulin receptor gene.
Desbois-Mouthon C, Magré J, Amselem S, Reynet C, Blivet MJ, Goossens M, Capeau J, Besmond C. Desbois-Mouthon C, et al. Among authors: capeau j. J Clin Endocrinol Metab. 1995 Jan;80(1):314-9. doi: 10.1210/jcem.80.1.7829633. J Clin Endocrinol Metab. 1995. PMID: 7829633
Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptor.
Desbois-Mouthon C, Danan C, Amselem S, Blivet-Van Eggelpoel MJ, Sert-Langeron C, Goossens M, Besmond C, Capeau J, Caron M. Desbois-Mouthon C, et al. Among authors: capeau j. Metabolism. 1996 Dec;45(12):1493-500. doi: 10.1016/s0026-0495(96)90178-x. Metabolism. 1996. PMID: 8969282
Major circadian variations of glucose homeostasis in a patient with Rabson-Mendenhall syndrome and primary insulin resistance due to a mutation (Cys284-->Tyr) in the insulin receptor alpha-subunit.
Desbois-Mouthon C, Magré J, Duprey J, Caron M, Blivet-Van Eggelpoel MJ, Daubas C, Gourmelen M, Chevallier B, Rizkalla S, Robert JJ, Capeau J. Desbois-Mouthon C, et al. Among authors: capeau j. Pediatr Res. 1997 Jul;42(1):72-7. doi: 10.1203/00006450-199707000-00012. Pediatr Res. 1997. PMID: 9212040
360 results