Primary hyperoxaluria type IWATTS, R. W. E.Quarterly journal of medicine. 1994, Vol 87, Num 10, pp 593-600, issn 0033-5622Article

Detection of AGXT gene mutations by denaturing high-performance liquid chromatography for diagnosis of hyperoxaluria type 1PIRULLI, D; GIORDANO, M; MOMIGLIANO-RICHIARDI, P et al.Clinical and experimental medicine (Testo stampato). 2001, Vol 1, Num 2, pp 99-104, issn 1591-8890, 6 p.Article

Subungual Oxalate Deposits in a Patient with Secondary HyperoxaluriaGREGORIOU, Stamatis; KALAPOTHAKOU, Kanella; KONTOCHRISTOPOULOS, George et al.Acta dermato-venereologica. 2011, Vol 91, Num 2, pp 195-196, issn 0001-5555, 2 p.Article

The effect of pyridoxine on oxalate dynamics in three cases of primary hyperoxaluria (with glycollic aciduria)WATTS, R. W. E; VEALL, N; PURKISS, P et al.Clinical science (1979). 1985, Vol 69, Num 1, pp 87-90, issn 0143-5221Article

Glyoxylate is a substrate of the sulfate-oxalate exchanger, sat-1, and increases its expression in HepG2 cellsSCHNEDLER, Nina; BURCKHARDT, Gerhard; BURCKHARDT, Birgitta C et al.Journal of hepatology. 2011, Vol 54, Num 3, pp 513-520, issn 0168-8278, 8 p.Article

Manifestations cutanées de l'hyperoxalurie primitive = Cutaneous manifestations of primary hyperoxaluriaZOUARI, N; ABROUG, S; BOUHLEL, R et al.Annales de dermatologie et de vénéréologie. 2008, Vol 135, Num 11, pp 796-797, issn 0151-9638, 2 p.Article

Primary hyperoxaluria in infants : Medical, ethical, and economic issuesCOCHAT, P; NOGUEIRA, P. C. K; AYMAN MAHMOUD, M et al.The Journal of pediatrics. 1999, Vol 135, Num 6, pp 746-750, issn 0022-3476Article

Epidemiology of primary hyperoxaluria type 1COCHAT, P; DELORAINE, A; ROTILY, M et al.Nephrology, dialysis, transplantation (Print). 1995, Vol 10, pp 3-7, issn 0931-0509, SUP8Conference Paper

Intérêt de la lithotritie extracorporelle dans l'hyperoxalurie primaire de type I = Effect of extracorporeal shock wave lithotripsy in primary hyperoxaluriaKAMOUN, A; CHEBIL, M; BEN HASSINE, L et al.Archives de pédiatrie (Paris). 1995, Vol 2, Num 8, pp 747-749, issn 0929-693XConference Paper

Molecular and cell biology of primary hyperoxaluria type 1DANPURE, C. J.The Clinical investigator. 1994, Vol 72, Num 9, pp 725-727, issn 0941-0198Conference Paper

A new case of hyperoxaluria type IIVILARINHO, L; ARAUJO, R; VILARINHO, A et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 5, pp 896-897, issn 0141-8955Article

High-performance liquid chromatographic microassay for L-alanine : glyoxylate aminotransferase activity in human liverPETRARULO, M; PELLEGRINO, S; MARANGELLA, M et al.Clinica chimica acta. 1992, Vol 208, Num 3, pp 183-192, issn 0009-8981Article

Plama oxalate and crating and oxalate/creatinine clearance ratios in normal subjects and in primary hyperoxaluria. Evidence for renal hyperoxaluriaKASIDAS, G. P; NEMAT, S; ROSE, G. A et al.Clinica chimica acta. 1990, Vol 191, Num 1-2, pp 67-77, issn 0009-8981, 11 p.Article

Treatment of renal failure in the primary hyperoxaluriasWATTS, R. W. E.Nephron. 1990, Vol 56, Num 1, pp 1-5, issn 0028-2766, 5 p.Article

The quantitation of oxalate in amniotic fluid by ion-chromatographyWANDZILAK, T. R; HANSON, F. W; WILLIAMS, H. E et al.Clinica chimica acta. 1989, Vol 185, Num 2, pp 131-137, issn 0009-8981Article

Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency)DANPURE, C. J; JENNINGS, P. R.Journal of inherited metabolic disease. 1988, Vol 11, pp 205-207, issn 0141-8955, suppl. 2Article

Chemical factors important to calcium nephrolithiasis: evidence for impaired hydroxycarboxylic acid absorption causing hyperoxaluriaCOWLEY, D. M; MCWHINNEY, B. C; BROWN, J. M et al.Clinical chemistry (Baltimore, Md.). 1987, Vol 33, Num 1, pp 243-247, issn 0009-9147Article

Primary hyperoxaluria type I: ultrastructural observations in liver biopsiesIANCU, T. C; DANPURE, C. J.Journal of inherited metabolic disease. 1987, Vol 10, Num 4, pp 330-338, issn 0141-8955Article

Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantationWATTS, R. W. E; ROLLES, K; MORGAN, S. H et al.Lancet (British edition). 1987, Num 8557, pp 474-475, issn 0140-6736Article

Always look beyond the stones: hyperoxaluria overlookedCHUNG, T. T; SUMMERS, S; SHEAFF, M et al.Clinical nephrology. 2004, Vol 62, Num 1, pp 58-61, issn 0301-0430, 4 p.Article

Primary hyperoxaluria type 2 without L-glycericaciduria : is the disease under-diagnosed?RUMSBY, Gill; SHARMA, Abhishek; CREGEEN, David P et al.Nephrology, dialysis, transplantation (Print). 2001, Vol 16, Num 8, pp 1697-1699, issn 0931-0509Article

Les formes infantiles de l'hyperoxalurie primaire de type I : à propos de quatre cas = Infantile primary hyperoxaluria type I : four casesKAMOUN, A; BEN MOUSSA, F; BEN MAIZ, H et al.Archives de pédiatrie (Paris). 1996, Vol 3, Num 10, pp 997-1000, issn 0929-693XArticle

Pathological case of the monthCHESNEY, R; FRIEDMAN, A; GILBERT-BARNESS, E et al.American journal of diseases of children (1960). 1992, Vol 146, Num 2, pp 255-256, issn 0002-922XArticle

Ocular histopathologic findings in a 46-year-old man with primary hyperoxaluriaSAKAMOTO, T; MAEDA, K; SUEISHI, K et al.Archives of ophthalmology (1960). 1991, Vol 109, Num 3, pp 384-387, issn 0003-9950, 4 p.Article

The subcellular metabolism of glyoxylate in primary hyperoxaluria type 1: the relationship between glycine production and oxalate overproductionTHOMPSON, G. N; PURKISS, P; DANPURE, C. J et al.Journal of inherited metabolic disease. 1988, Vol 11, pp 212-214, issn 0141-8955, suppl. 2Article