Erbliche metabolische Nierenerkrankungen

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O'Regan PF et al. (1980) Primary hyperoxaluria.

Morris MC et al. (1982) Oxalosis in infancy.

Rajantie J et al. (1981) Lysinuric protein intolerance. Basolateral transport defect in renal tubuli.

Milliner DS et al. (1994) Results of long-term treatment with orthophosphate and pyridoxine in patients with primary hyperoxaluria.

Parto K et al. (1994) Pulmonary alveolar proteinosis and glomerulonephritis in lysinuric protein intolerance: case reports and autopsy findings of four pediatric patients.

None (1993) Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.

McManus DT et al. (1996) Necropsy findings in lysinuric protein intolerance.

Danpure CJ et al. (1996) Strategies for the prenatal diagnosis of primary hyperoxaluria type 1.

Parsons H et al. (1996) Immune complex disease consistent with systemic lupus erythematosus in a patient with lysinuric protein intolerance.

Lauteala T et al. (1997) Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14.

Kemper MJ et al. (1997) Primary hyperoxaluria type 2.

None (1998) Preemptive liver transplantation from a living related donor for primary hyperoxaluria type I.

Lauteala T et al. () Genetic homogeneity of lysinuric protein intolerance.

Duval M et al. (1999) Intermittent hemophagocytic lymphohistiocytosis is a regular feature of lysinuric protein intolerance.