Homocystinuria.
作者信息
Cusworth D C, Dent C E
出版信息
Biochem J. 1969 Feb;111(3):1P-2P. doi: 10.1042/bj1110001p.
Abstract
摘要
相似文献
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The biosynthesis of cystathionine in patients with homocystinuria.同型胱氨酸尿症患者中胱硫醚的生物合成。
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Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxine.由于胱硫醚合成酶缺乏所致的同型胱氨酸尿症：维生素B6的作用。
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本文引用的文献
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HOMOCYSTINURIA. STUDIES OF 20 FAMILIES WITH 38 AFFECTED MEMBERS.同型胱氨酸尿症。对20个家庭中38名患者的研究。
JAMA. 1965 Aug 30;193:711-9. doi: 10.1001/jama.1965.03090090017003.
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HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS.同型胱氨酸尿症：3例患者的代谢研究
J Pediatr. 1965 Jul;67:58-68. doi: 10.1016/s0022-3476(65)80304-3.
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HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.同型胱氨酸尿症：10例临床与病理回顾
J Pediatr. 1965 Mar;66:565-83. doi: 10.1016/s0022-3476(65)80121-4.
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HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE.由于胱硫醚合成酶缺乏导致的同型胱氨酸尿症：遗传方式。
Science. 1964 Nov 6;146(3645):785-7. doi: 10.1126/science.146.3645.785.
5
PATHOLOGICAL FINDINGS IN HOMOCYSTINURIA.同型胱氨酸尿症的病理发现
J Clin Pathol. 1964 Jul;17(4):427-37. doi: 10.1136/jcp.17.4.427.
6
HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN.同型胱氨酸尿症：大脑中缺乏胱硫醚。
Science. 1964 Aug 7;145(3632):588. doi: 10.1126/science.145.3632.588.
7
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.同型胱氨酸尿症：一种酶缺陷。
Science. 1964 Mar 27;143(3613):1443-5. doi: 10.1126/science.143.3613.1443.
8
HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.同型胱氨酸尿症：一种与智力缺陷相关的新的先天性代谢紊乱。
Arch Dis Child. 1963 Oct;38(201):425-36. doi: 10.1136/adc.38.201.425.
9
Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.在北爱尔兰对智力落后个体的一项调查中检测到的代谢异常。
Arch Dis Child. 1962 Oct;37(195):505-13. doi: 10.1136/adc.37.195.505.
10
The identification of homocystine in the urine.尿液中同型胱氨酸的鉴定。
Biochem Biophys Res Commun. 1962 Dec 19;9:493-6. doi: 10.1016/0006-291x(62)90114-6.
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