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2. Nonacidotic proximal tubulopathy transmitted as autosomal dominant trait. Vezzoli G; Zerbi S; Baragetti I; Soldati L; Mora S; Dell'Antonio G; Bianchi G Am J Kidney Dis; 1997 Apr; 29(4):490-5. PubMed ID: 9100036 [TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive renal proximal tubulopathy and hypercalciuria: a new syndrome. Magen D; Adler L; Mandel H; Efrati E; Zelikovic I Am J Kidney Dis; 2004 Apr; 43(4):600-6. PubMed ID: 15042536 [TBL] [Abstract][Full Text] [Related]
4. Renal hypouricemia and absorptive hypercalciuria: a real syndrome. Uribarri J; Oh MS Nephron; 1993; 63(2):172-5. PubMed ID: 8450908 [TBL] [Abstract][Full Text] [Related]
5. [Renal tubular function in children with hypercalciuria]. Kovacević L; Kovacević S; Smoljanić Z; Kostić M; Peco-Antić A; Gajić M; Kovacević M; Jovanović O Srp Arh Celok Lek; 1998; 126(7-8):223-7. PubMed ID: 9863386 [TBL] [Abstract][Full Text] [Related]
6. Proximal tubular defects in idiopathic hypercalciuria: resistance to phosphate administration. Lau YK; Wasserstein A; Westby GR; Bosanac P; Grabie M; Mitnick P; Slatopolsky E; Goldfarb S; Agus ZS Miner Electrolyte Metab; 1982; 7(5):237-49. PubMed ID: 7169988 [TBL] [Abstract][Full Text] [Related]
7. Combined proximal tubulopathy, crystal-storing histiocytosis, and cast nephropathy in a patient with light chain multiple myeloma. Wu CK; Yang AH; Lai HC; Lin BS BMC Nephrol; 2017 May; 18(1):170. PubMed ID: 28545410 [TBL] [Abstract][Full Text] [Related]
9. Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush border. Manz F; Waldherr R; Fritz HP; Lutz P; Nützenadel W; Reitter B; Schärer K; Schmidt H; Trefz F Clin Nephrol; 1984 Sep; 22(3):149-57. PubMed ID: 6488596 [TBL] [Abstract][Full Text] [Related]
10. The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndrome. Steinmann B; Bachmann C; Colombo JP; Gitzelmann R Pediatr Res; 1987 Feb; 21(2):201-4. PubMed ID: 3822602 [TBL] [Abstract][Full Text] [Related]
11. Loss of tubular creatinine secretion as the only sign of tubular proximal cell dysfunction in light chain proximal tubulopathy: A case report. Stehlé T; Vignon M; Flamant M; Figueres ML; Rabant M; Rodenas A; Noël LH; Arnulf B; Vidal-Petiot E Medicine (Baltimore); 2016 Jun; 95(26):e3815. PubMed ID: 27367983 [TBL] [Abstract][Full Text] [Related]
12. A monoclonal V kappa l light chain responsible for incomplete proximal tubulopathy. Decourt C; Bridoux F; Touchard G; Cogné M Am J Kidney Dis; 2003 Feb; 41(2):497-504. PubMed ID: 12552516 [TBL] [Abstract][Full Text] [Related]
13. Familial hypouricemia due to isolated renal tubular defect. Attenuated response of uric acid clearance to probenecid and pyrazinamide. Benjamin D; Sperling O; Weinberger A; Pinkhas J; de Vries A Nephron; 1977; 18(4):220-5. PubMed ID: 854144 [TBL] [Abstract][Full Text] [Related]
14. Glomerular, Mesangial, and Tubular Cytoplasmic Fibrillary Inclusions in a Patient with Light-Chain Proximal Tubulopathy. Chung EYM; McIlroy K; Fung C; Seshan SV; Moran S; Coleman PL Nephron; 2020; 144(4):190-194. PubMed ID: 32018256 [TBL] [Abstract][Full Text] [Related]
15. Effect of luminal pH and HCO3- on phosphate reabsorption in the rabbit proximal convoluted tubule. Hamm LL; Kokko JP; Jacobson HR Am J Physiol; 1984 Jul; 247(1 Pt 2):F25-34. PubMed ID: 6331202 [TBL] [Abstract][Full Text] [Related]
16. Familial glomerulopathy with proximal tubular dysfunction: a new syndrome? Mattoo TK; Akhtar M Pediatr Nephrol; 1990 May; 4(3):223-7. PubMed ID: 2400648 [TBL] [Abstract][Full Text] [Related]
17. Hypouricaemia and proximal renal tubular dysfunction in acute myeloid leukaemia. Mir MA; Delamore IW Br Med J; 1974 Sep; 3(5934):775-7. PubMed ID: 4528597 [TBL] [Abstract][Full Text] [Related]