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Glucuronic acid conjugation by patients with familial nonhemolytic jaundice and their relatives.

作者信息

CHILDS B, SIDBURY J B, MIGEON C J

出版信息

Pediatrics. 1959 May;23(5):903-13.

PMID:13645126
Abstract
摘要

相似文献

1
Glucuronic acid conjugation by patients with familial nonhemolytic jaundice and their relatives.
Pediatrics. 1959 May;23(5):903-13.
2
Studies of glucuronidation in 3 infants with familial congenital nonhemolytic jaundice.
J Pediatr. 1962 Aug;61:303-4. doi: 10.1016/s0022-3476(62)80286-8.
3
[Glucuronic acid conjugation of 4-14C-cortisol metabolites in icterus intermittens juvenilis].
Nord Med. 1966 Feb 17;75(7):179-81.
4
[Urinary elimination of glucuronic acid and blood bilirubin levels in premature infants].
Minerva Pediatr. 1959 Mar 24;11(12):316-7.
5
Administration of glucuronic acid to icteric newborn infants.
Pediatrics. 1959 Jan;23(1 Pt 1):92-7.
6
A clinical syndrome associated with a defect in steroid glucuronide formation.
J Clin Endocrinol Metab. 1957 Dec;17(12):1485-8. doi: 10.1210/jcem-17-12-1485.
7
[Study on the capacity of glucuro-conjugation in the premature newborn infant. Evaluation of the urinary elimination of glucuronic acid after loading with acetyl-salicylic acid].
Clin Radiol. 1960 Nov;42:1027-36.
8
Estimation of bilirubin mono- and diglucuronide in the plasma and urine of patients with nonhemolytic jaundice.
J Lab Clin Med. 1959 Apr;53(4):557-62.
9
Possible structure-induced shift from amino acid to glucuronic acid conjugation of arylacetic acids in the cat [proceedings].
West Afr J Pharmacol Drug Res. 1977 Jun;4(1):57P-59P.
10
[BEHAVIOR OF GLUCURONIC ACID IN MECHANICAL JAUNDICE].
Pol Arch Med Wewn. 1963;33:1269-74.

引用本文的文献

1
[Advances in the recognition of heterozygous characteristics in hereditary enzymopathies].[遗传性酶病杂合子特征识别的进展]
Klin Wochenschr. 1962 Jun 1;40:553-8. doi: 10.1007/BF01478627.
2
Jaundice and bilirubin metabolism.黄疸与胆红素代谢。
Bull N Y Acad Med. 1959 Dec;35(12):755-64.
3
ON THE RATE OF FORMATION OF STERIDAL GLUCURONOSIDES IN PATIENTS WITH FAMILIAL AND ACQUIRED JAUNDICE.关于家族性和获得性黄疸患者甾体葡萄糖醛酸苷的形成速率
J Clin Invest. 1964 Oct;43(10):1952-67. doi: 10.1172/JCI105069.
4
INHERITED ENZYME DEFECTS: A REVIEW.遗传性酶缺陷：综述
J Clin Pathol. 1963 Jul;16(4):293-318. doi: 10.1136/jcp.16.4.293.
5
Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults.青少年及成人中无明显溶血迹象的慢性非结合胆红素血症。
J Clin Invest. 1962 Dec;41(12):2233-45. doi: 10.1172/JCI104682.
6
Neonatal hyperbilirubinaemia.新生儿高胆红素血症
Br Med J. 1960 May 21;1(5185):1528-34. doi: 10.1136/bmj.1.5185.1528.
7
Crigler-Najjar syndrome type II. New observation of possible autosomal recessive inheritance.克里格勒-纳贾尔综合征II型。常染色体隐性遗传可能性的新观察。
Dig Dis Sci. 1995 Jan;40(1):28-32. doi: 10.1007/BF02063937.
8
[Cerebral lesions in congenital nonhemolytic jaundice (Crigler-Najjar syndrome)].[先天性非溶血性黄疸（克里格勒 - 纳贾尔综合征）中的脑病变]
Acta Neuropathol. 1970;16(2):141-7. doi: 10.1007/BF00687668.
9
Criggler-Najjar syndrome. Report of a case.
Indian J Pediatr. 1971 Jan;38(276):39-41. doi: 10.1007/BF02787650.
10
Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.在一名I型克里格勒-纳贾尔综合征患者的UGT1基因复合体中，鉴定出胆红素UDP-葡萄糖醛酸基转移酶编码中的一种基因改变。
J Clin Invest. 1992 Jul;90(1):150-5. doi: 10.1172/JCI115829.