2,8-Dihydroxyadenine crystalluria vs urolithiasisLAXDAL, T.Lancet (British edition). 1992, Vol 340, Num 8812, issn 0140-6736, p. 184Article

Adenine phosphoribosyltransferase deficiency in IcelandLAXDAL, T; JONASSON, T. A.Acta medica Scandinavica. 1988, Vol 224, Num 6, pp 621-626, issn 0001-6101Article

Adenine phosphoribosyltransferase deficiency: a case diagnosed by GC-MS identification of 2,8-dihydroxyadenine in urinary crystalsCHRISTENSEN, E; BRANDT, N. J; LAXDAL, T et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 2, pp 187-194, issn 0141-8955Article

Cutis marmorata telangiectatica congenita with terminal transverse limb defectsBJORNSDOTTIR, U. S; LAXDAL, T; BJORNSSON, J et al.Acta paediatrica scandinavica. 1988, Vol 77, Num 5, pp 780-782, issn 0001-656XArticle

Type 4 renal tubular acidosis (sub-type 2) associated with idiopathic interistitial nephritisKRISTJANSSON, K; LAXDAL, T; RAGNARSSON, J et al.Acta paediatrica scandinavica. 1986, Vol 75, Num 6, pp 1051-1054, issn 0001-656XArticle

Acute renal failure in a middle-aged woman with 2,8-dihydroxyadeninuriaARNADOTTIR, M; LAXDAL, T; HARDARSON, S et al.Nephrology, dialysis, transplantation (Print). 1997, Vol 12, Num 9, pp 1985-1987, issn 0931-0509Article

Identification of a single missense mutation in the adenine phosphoribosyltransferase (APRT) gene from five Icelandic patients and a British patientCHEN, J; SAHOTA, A; LAXDAL, T et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1306-1311, issn 0002-9297Article

Congenital cardiomyopathy and cataracts with lactic acidosisVALSSON, J; LAXDAL, T; JONSSON, A et al.The American journal of cardiology. 1988, Vol 61, Num 1, pp 193-194, issn 0002-9149Article