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• 1.Santer R, Calado J. Familial renal glucosuria and SGLT2: from a mendelian trait to a therapeutic target. Clin J Am Soc Nephrol 2010; 5: 133-41.
• 2.Marble A. Incidence of glycosuria and diabetes. Med Clin N Am 1947; 31: 313.
• 3.Wilgen U, Cobb H. An unusual cause of glycosuria in a 5-year -old child. SAJCH 2008; 2: 134-5.
• 4.Calado J, Santer R, Rueff J. Effect of kidney disease on glucose handling (including genetic defects). Kidney Int Suppl 2011: 7-13. PMID: 21358700.
• 5.Lee H, Han KH, Park HW, et al. Familial renal glucosuria: a clinicogenetic study of 23 additional cases. Pediatr Nephrol 2012; 27: 1091-5.
• 6.Calado J, Sznajer Y, Metzger D, et al. Twenty-one additional cases of familial renal glucosuria: Absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Nephrol Dial Transplant 2008; 23: 3874-9.
• 7.Wright EM, Hirayama BA, Loo DF Active sugar transport in health and disease. J Intern Med 2007; 261: 32-43.
• 8.De Marchi S, Cecchin E, Basile A, et al. Is renal glycosuria a benin condition? Proc Eur Dial Transplant Assoc 1983; 20: 681-5.
• 9.Sankarasubbaiyan S, Cooper C, Heilig CW. Identification of a novel form of renal glucosuria with overexcretion of arginine, carnosine, and taurine. Am J Kidney Dis 2001; 37: 1039-43.