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2. Phenotype and genotype of Dent's disease in three Chinese boys. Li P; Huang JP Nephrology (Carlton); 2009 Apr; 14(2):139-42. PubMed ID: 19076289 [TBL] [Abstract][Full Text] [Related]
3. Truncating mutations in the chloride/proton ClC-5 antiporter gene in Seven Jewish Israeli families with Dent's 1 disease. Dinour D; Davidovitz M; Levin-Iaina N; Lotan D; Cleper R; Weissman I; Knecht A; Holtzman EJ Nephron Clin Pract; 2009; 112(4):c262-7. PubMed ID: 19546586 [TBL] [Abstract][Full Text] [Related]
4. Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease. Ludwig M; Utsch B; Monnens LA Nephrol Dial Transplant; 2006 Oct; 21(10):2708-17. PubMed ID: 16861240 [No Abstract] [Full Text] [Related]
5. [Dent's disease]. Pavićević S; Bogdanović R; Ludwig M; Samardzić M Srp Arh Celok Lek; 2008 Dec; 136 Suppl 4():312-5. PubMed ID: 20804101 [TBL] [Abstract][Full Text] [Related]
10. Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg? Frishberg Y; Dinour D; Belostotsky R; Becker-Cohen R; Rinat C; Feinstein S; Navon-Elkan P; Ben-Shalom E Pediatr Nephrol; 2009 Dec; 24(12):2369-73. PubMed ID: 19806368 [TBL] [Abstract][Full Text] [Related]
11. Can we generate new hypotheses about Dent's disease from gene analysis of a mouse model? Guggino SE Exp Physiol; 2009 Feb; 94(2):191-6. PubMed ID: 18931044 [TBL] [Abstract][Full Text] [Related]
12. [Dent's disease: hereditary nephrolithiasis related to defective tubular endocytosis processes]. Tosetto E; Anglani F; Graziotto R; Citron L; D'Angelo A; Gambaro G G Ital Nefrol; 2003; 20(6):578-88. PubMed ID: 14732909 [TBL] [Abstract][Full Text] [Related]
13. Cause of hypercalciuria in X-linked chloride channel gene mutations. Donckerwolcke R; Gerver WJ Pediatr Nephrol; 2000 Feb; 14(2):179-82. PubMed ID: 10787236 [No Abstract] [Full Text] [Related]
14. CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's disease. Besbas N; Ozaltin F; Jeck N; Seyberth H; Ludwig M Nephrol Dial Transplant; 2005 Jul; 20(7):1476-9. PubMed ID: 15814539 [No Abstract] [Full Text] [Related]
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17. Mining the x-chromosome for disease genes by deep resequencing. McCabe ER Pediatr Res; 2009 Jul; 66(1):2. PubMed ID: 19542828 [No Abstract] [Full Text] [Related]
18. [Infrequent X chromosome abnormality and X-linked syndromic deafness]. Wang YJ; Shi XL; Nie JW; Ni B; Yin ZC; Dai HP Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2004 Oct; 29(5):500-3. PubMed ID: 16137031 [TBL] [Abstract][Full Text] [Related]
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20. Decoding Hypercalcemia and Renal Stones in a Young Adult: Could it be Dent's Disease? Hajji M; Kaaroud H; Ben Hamida F; Abderrahim E Clin Med Insights Case Rep; 2023; 16():11795476231182591. PubMed ID: 37435354 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]