| Nr. | Year OPEN | Title | users say | rate good | rate bad | no link | Citation |
|---|
OxalosisNephrolithiasisNephrocalcinosisFructose intoleranceLesch Nyhan syndromeMitochondria (Mitochondriopathy)Wilson s diseaseCystinosisTyrosinemiaXanthinePhosphoribosylpyrophosphate synthetaseFanconi s syndromeCystinuriaAdenine phosphoribosyl transferaseMetabolomicsEndosymbiosisEvolutionProtein (Transport)PexophagyAlanine glyoxylate aminotransferase| 1 | 2004 | Persistent cutaneous manifestations of hyperoxaluria after combined hepatorenal transplantation. | 
| + | - | nl | Dermatol Online J 10(1):10 (2004) |
| 2 | 2000 | Current approaches to the management of primary hyperoxaluria. |
| + | - | nl | Arch Dis Child 82(6):470-3 (2000) |
| 3 | 2001 | The primary hyperoxalurias. |
| + | - | nl | J Am Soc Nephrol 12(9):1986-93 (2001) |
| 4 | 1977 | Histopathological occurrence and characterisation of calcium oxalate: a review. |
| + | - | nl | J Clin Pathol 30(9):800-11 (1977) |
| 5 | 2008 | Recurrence of primary hyperoxaluria: an avoidable catastrophe following kidney transplant. |
| + | - | nl | J Postgrad Med 54(3):206-8 (2008) |
| 6 | 1999 | Primary hyperoxaluria type 1. |
| + | - | nl | Kidney Int 55(6):2533-47 (1999) |
| 7 | 2005 | Primary hyperoxaluria: from gene defects to designer drugs? |
| + | - | nl | Nephrol Dial Transplant 20(8):1525-9 (2005) |
| 8 | 2003 | Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome. |
| + | - | nl | Nephrol Dial Transplant 18(2):273-9 (2003) |
| 9 | 2005 | Development of a physiologically based pharmacokinetic model for ethylene glycol and its metabolite, glycolic Acid, in rats and humans. |
| + | - | nl | Toxicol Sci 85(1):476-90 (2005) |
| 10 | 1996 | Initial manifestation of primary hyperoxaluria type I in adults-- recognition, diagnosis, and management. |
| + | - | nl | West J Med 164(1):42-53 (1996) |
| 11 | 1991 | Primary hyperoxaluria: therapeutic strategies for the 90's. |
| + | - | nl | Kidney Int 40(3):389-99 (1991) |
| 12 | 1978 | Oxalic acid and the hyperoxaluric syndromes. |
| + | - | nl | Kidney Int 13(5):410-7 (1978) |
| 13 | 2004 | Type 1 primary hyperoxaluria in pediatric patients: renal sonographic patterns. |
| + | - | nl | AJR Am J Roentgenol 183(6):1767-70 (2004) |
| 14 | 2005 | Molecular etiology of primary hyperoxaluria type 1: new directions for treatment. |
| + | - | nl | Am J Nephrol 25(3):303-10 (2005) |
| 15 | 2004 | Diagnostic and therapeutic strategies in hyperoxaluria: a plea for early intervention. |
| + | - | nl | Nephrol Dial Transplant 19(1):39-42 (2004) |
| 16 | 2010 | Diagnostic examination of the child with urolithiasis or nephrocalcinosis. |
| + | - | nl | Pediatr Nephrol 25(3):403-13 (2010) |
| 17 | 2010 | Nephrolithiasis related to inborn metabolic diseases. | 
| + | - | nl | Pediatr Nephrol 25(3):415-24 (2010) |
| 18 | 2010 | Cardiac abnormalities in primary hyperoxaluria. |
| + | - | nl | Circ J 74(11):2403-9 (2010) |
| 19 | 2010 | Evolutionary origins of metabolic compartmentalization in eukaryotes. |
| + | - | nl | Philos Trans R Soc Lond B Biol Sci 365(1541):847-55 (2010) Martin W |
| 20 | 2010 | Molecular mechanism and physiological role of pexophagy. |
| + | - | nl | FEBS Lett 584(7):1367-73 (2010) |
| 21 | 2011 | Studies on a unique organelle localization of a liver enzyme, serine:pyruvate (or alanine:glyoxylate) aminotransferase. |
| + | - | nl | Proc Jpn Acad Ser B Phys Biol Sci 87(5):274-86 (2011) |
