| Hoopes Jr, Richard R; Raja, Khalid M; Koich, April et al. (2004) Evidence for genetic heterogeneity in Dent's disease. Kidney Int 65:1615-20 |
| Knohl, Stephen J; Scheinman, Steven J (2004) Inherited hypercalciuric syndromes: Dent's disease (CLC-5) and familial hypomagnesemia with hypercalciuria (paracellin-1). Semin Nephrol 24:55-60 |
| Norden, Anthony G W; Lapsley, Marta; Igarashi, Takashi et al. (2002) Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome. J Am Soc Nephrol 13:125-33 |
| Raja, Khalid A; Schurman, Scott; D'mello, Richard G et al. (2002) Responsiveness of hypercalciuria to thiazide in Dent's disease. J Am Soc Nephrol 13:2938-44 |
| Norden, A G; Lapsley, M; Lee, P J et al. (2001) Glomerular protein sieving and implications for renal failure in Fanconi syndrome. Kidney Int 60:1885-92 |
| Norden, A G; Scheinman, S J; Deschodt-Lanckman, M M et al. (2000) Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases. Kidney Int 57:240-9 |
| Scheinman, S J; Cox, J P; Lloyd, S E et al. (2000) Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria. Kidney Int 57:232-9 |
| Scheinman, S J (1999) Nephrolithiasis. Semin Nephrol 19:381-8 |
| Scheinman, S J; Guay-Woodford, L M; Thakker, R V et al. (1999) Genetic disorders of renal electrolyte transport. N Engl J Med 340:1177-87 |
| Schurman, S J; Norden, A G; Scheinman, S J (1998) X-linked recessive nephrolithiasis: presentation and diagnosis in children. J Pediatr 132:859-62 |
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