共 264 条
- [1] Hoppe B(2012)An update on primary hyperoxaluria Nat Rev Nephrol 8 467-475
- [2] Martin-Higueras C(2017)Molecular therapy of primary hyperoxaluria J Inherit Metab Dis 40 481-489
- [3] Torres A(2019)Molecular basis of primary hyperoxaluria: clues to innovative treatments Urolithiasis 47 67-78
- [4] Salido E(2012)Primary hyperoxalurias: disorders of glyoxylate detoxification Biochim Biophys Acta 1822 1453-1464
- [5] Dindo M(2009)Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene Hum Mutat 30 910-917
- [6] Conter C(2003)Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2 Hum Mutat 22 497-436
- [7] Oppici E(2016)Primary hyperoxaluria: a review Nephrol Ther 12 431-376
- [8] Ceccarelli V(2012)Extreme intrafamilial variability of Saudi brothers with primary hyperoxaluria type 1 Ther Clin Risk Manag 8 373-e44
- [9] Marinucci L(2004)Molecular aetiology of primary hyperoxaluria type 1 Nephron Exp Nephrol 98 e39-1081
- [10] Cellini B(2006)Primary hyperoxaluria type 1: still challenging! Pediatr Nephrol 21 1075-455