Primary hyperoxaluria type 1: Gene therapy by liver transplantation

Transplantation

Volumn 87, Issue 9, 2009, Pages 1273-1274

  Jamieson, Neville V ^a   Jamieson, Katharine A ^a  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE GLYOXYLATE AMINOTRANSFERASE;

AUTOSOMAL RECESSIVE INHERITANCE; CADAVER DONOR; EARLY DIAGNOSIS; EUROPE; GENE THERAPY; GENOTYPE PHENOTYPE CORRELATION; GLOMERULUS FILTRATION RATE; GROWTH RETARDATION; HEMOPHILIA; HUMAN; KAPLAN MEIER METHOD; KIDNEY CALCIFICATION; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; LIVER TRANSPLANTATION; NOTE; OBSTRUCTIVE UROPATHY; OXALOSIS 1; PRIORITY JOURNAL; REGISTER; RENAL REPLACEMENT THERAPY; SURVIVAL RATE;

CHILD; COMBINED MODALITY THERAPY; GENE THERAPY; HUMANS; HYPEROXALURIA, PRIMARY; LIVER TRANSPLANTATION; SURVIVAL RATE; SURVIVORS; TISSUE DONORS; TREATMENT OUTCOME;

EID: 67649628409     PISSN: 00411337     EISSN: None     Source Type: Journal    
DOI: 10.1097/TP.0b013e3181a17157     Document Type: Note

References (5)

1. Danpure CJ. Molecular aetiology of primary hyperoxaluria type 1: New directions for treatment. Am J Nephrol 2005; 25: 303.
2. Cochat PA, Deloraine A, Rotily M, et al. Epidemiology of primary hyperoxaluria type 1. Nephrol Dial Transplant 1995; 10(suppl 8): 3.
3. Farese S, Trost N, Candinas D, et al. Early renal failure after domino hepatic transplantation using the liver from a compound heterozygous patient with primary hyperoxaluria. Nephrol Dial Transplant 2005; 20: 2557.
4. Jamieson NV. A 20-year experience of combined liver/kidney transplantation for primary hyperoxaluria (PH1): The European PH1 Transplant Registry Experience 1984-2004. Am J Nephrol 2005; 25:282.
5. Watts RW, Calne RY, Williams R, et al. Primary hyperoxaluria (type I): Attempted treatment by combined hepatic and renal transplantation. Q J Med 1985; 57: 697.