一名黄嘌呤尿症和嗜铬细胞瘤患者的临床、生理及生化研究 - Suppr

CLINICAL, PHYSIOLOGICAL AND BIOCHEMICAL STUDIES OF A PATIENT WITH XANTHINURIA AND PHEOCHROMOCYTOMA.

作者信息

ENGELMAN K, WATTS R W, KLINENBERG J R, SJOERDSMA A, SEEGMILLER J E

出版信息

Am J Med. 1964 Dec;37:839-61. doi: 10.1016/0002-9343(64)90128-7.

DOI:10.1016/0002-9343(64)90128-7

PMID:14246087

Abstract

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CLINICAL, PHYSIOLOGICAL AND BIOCHEMICAL STUDIES OF A PATIENT WITH XANTHINURIA AND PHEOCHROMOCYTOMA.

Am J Med. 1964 Dec;37:839-61. doi: 10.1016/0002-9343(64)90128-7.

THE STUDY OF PURINE UTILIZATION AND EXCRETION IN A XANTHINURIC MAN.

J Clin Invest. 1965 Jul;44(7):1248-60. doi: 10.1172/JCI105231.

ENZYME DEFECT IN A CASE OF XANTHINURIA.

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Xanthinuria: an additional case with demonstration of xanthine oxidase deficiency.

Am J Clin Pathol. 1971 Mar;55(3):351-4. doi: 10.1093/ajcp/55.3.351.

[Hereditary xanthinuria. A clinical case report].

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Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria.

Clin Chim Acta. 1984 Feb 28;137(2):189-98. doi: 10.1016/0009-8981(84)90179-7.

[Three cases of hereditary xanthinuria: review of the literature (author's transl)].

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[The total absence of xanthine oxidase activity. Apropos 2 cases of the nonfamilial incidence of xanthinuria].

An Med Interna. 1991 Apr;8(4):181-4.

[Hypouricemia and xanthinuria. Observation of 3 cases].

Minerva Med. 1979 Mar 10;70(12):873-8.

[Xanthine oxidase deficiency (hereditary xanthinuria), molybdenum cofactor deficiency].

Nihon Rinsho. 1996 Dec;54(12):3333-6.

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CLINICAL, PHYSIOLOGICAL AND BIOCHEMICAL STUDIES OF A PATIENT WITH XANTHINURIA AND PHEOCHROMOCYTOMA.

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