Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.
作者信息
Laster L, Mudd S H, Finkelstein J D, Irreverre F
出版信息
J Clin Invest. 1965 Oct;44(10):1708-19. doi: 10.1172/JCI105278.
Abstract
摘要
相似文献
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Homocystinuria due to cystathionine synthase deficiency: the metabolism of L-methionine.由于胱硫醚β-合酶缺乏导致的同型胱氨酸尿症：L-蛋氨酸的代谢
J Clin Invest. 1965 Oct;44(10):1708-19. doi: 10.1172/JCI105278.
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[Biochemical aspects of some congenital anomalies of the metabolism of sulfur amino acids].
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Homocystinuria due to cystathionine synthase deficiency: enzymatic and ultrastructural studies.由于胱硫醚合成酶缺乏所致的同型胱氨酸尿症：酶学及超微结构研究
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The relation of sulfur metabolism to acid-base balance and electrolyte excretion: the effects of DL-methionine in normal man.硫代谢与酸碱平衡及电解质排泄的关系：DL-蛋氨酸对正常人的影响。
J Clin Invest. 1959 Dec;38(12):2215-23. doi: 10.1172/JCI104001.
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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. BIOCHEMICAL STUDIES OF TISSUES INCLUDING A COMPARISON WITH CYSTATHIONINURIA.同型胱氨酸尿症。组织的生化研究，包括与胱硫醚尿症的比较。
Pediatrics. 1965 Jan;35:50-6.
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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。
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PATHOLOGICAL FINDINGS IN HOMOCYSTINURIA.同型胱氨酸尿症的病理发现
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HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN.同型胱氨酸尿症：大脑中缺乏胱硫醚。
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HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE.同型胱氨酸尿症，一种甲硫氨酸代谢紊乱疾病。
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HOMOCYSTINURIA, THROMBOSIS, AND THE BLOOD-PLATELETS.
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HOMOCYSTINURIA: AN ENZYMATIC DEFECT.同型胱氨酸尿症：一种酶缺陷。
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