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LITHIASE XANTHIQUE CHEZ L'ENFANT: A PROPOS D'UN CAS, REVUE DE LA LITTERATURELANSON Y; ROBERT M; MAURAGE C et al.1978; J. UROL. NEPHROL.; FRA; DA. 1978; VOL. 84; NO 7-8; PP. 527-538; ABS. ENG; BIBL. 40 REF.Article

TWO SUCCESSIVE PREGNANCIES IN A WOMAN WITH XANTHINURIA: UNEXPECTED INCREASE IN SERUM URIC ACID LEVELSUZAN S; BEAUFILS M; RAGOT J et al.1980; J. PERINAT. MED.; ISSN 0300-5577; DEU; DA. 1980; VOL. 8; NO 6; PP. 284-287; ABS. GER/FRE; BIBL. 6 REF.Article

XANTHINE NEPHROPATHY DURING CHEMOTHERAPY IN DEFICIENCY OF HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE.GOMEZ GA; STUTZMAN L; MING CHU T et al.1978; ARCH. INTERN. MED.; USA; DA. 1978; VOL. 138; NO 6; PP. 1017-1019; BIBL. 9 REF.Article

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CALCUL DE XANTHINE ET XANTHINURIE LIES A L'URETERE RETROCAVE: PRESENTATION D'UN CAS ET REVUE DE LA LITTERATUREKITAMURA T; KAWAMURA T; KITAGAWA R et al.1976; JAP. J. UROL.; JAP.; DA. 1976; VOL. 67; NO 8; PP. 670-676; ABS. ANGL.; BIBL. 1 P. 1/2Article

Hereditary xanthinuria presenting in infancy with nephrolithiasisCARPENTER, T. O; LEBOWITZ, R. L; NELSON, D et al.The Journal of pediatrics. 1986, Vol 109, Num 2, pp 307-309, issn 0022-3476Article

Hereditary xanthinuria in 2 Pakistani sisters: asymptomatic in one with β-thalassemia but causing xanthine stone, obstructive uropathy and hypertension in the otherMAYNARD, J; BENSON, P.The Journal of urology. 1988, Vol 139, Num 2, pp 338-339, issn 0022-5347Article

Hereditary xanthinuria: evidence for enhanced hypoxanthine salvageMATEOS, F. A; PUIG, J. G; JIMENEZ, M. L et al.The Journal of clinical investigation. 1987, Vol 79, Num 3, pp 847-852, issn 0021-9738Article

Separation and quantitation of oxypurines by isocratic high-pressure liquid chromatography: application to xanthinuria and the Lesch-Nyhan syndromeCRAWHALL, J. C; ITIABA, K; KATZ, S et al.Biochemical medicine. 1983, Vol 30, Num 2, pp 261-270, issn 0006-2944Article

STUDY OF URINARY PYRAZINAMIDE METABOLITES AND THEIR ACTION ON THE RENAL EXCRETION OF XANTHINE AND HYPOXANTHINE IN A XANTHINURIC PATIENT.AUSCHER C; PASQUIER C; PEHUET P et al.1978; BIOMEDICINE; FRA; DA. 1978; VOL. 28; NO 2; PP. 129-133; BIBL. 17 REF.Article

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Lithiases urinaires récidivantes révélant une xanthinurie héréditaire = Recurrent urinary lithiasis revealing hereditary xanthinuriaBAHLOUS, Afef; GASMI, Manef; MOHSNI, Amira et al.La Presse médicale (1983). 2007, Vol 36, Num 9, pp 1203-1206, issn 0755-4982, 4 p., CAH1Article

Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxipurinolREITER, S; SIMMONDS, H. A; ZOLLNER, N et al.Clinica chimica acta. 1990, Vol 187, Num 3, pp 221-234, issn 0009-8981Article

A Chinese case of hereditary xanthinuriaCHU, T.-S; LIU, Y.-L; YEN, T.-S et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 5, issn 0141-8955, p. 899Article

A new case with hereditary xanthinuria: response to exerciseLANDAAS, S; BORCH, K; AAGAARD, E et al.Clinica chimica acta. 1989, Vol 181, Num 2, pp 119-124, issn 0009-8981Article