Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects.
作者信息
MATTHEWS W B
出版信息
Proc R Soc Med. 1958 Oct;51(10):859-63. doi: 10.1177/003591575805101014.
Abstract
摘要
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Discussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspects.神经系统代谢紊乱的一些临床、遗传和生化方面的探讨：神经系统代谢疾病：临床方面
Proc R Soc Med. 1958 Oct;51(10):859-63. doi: 10.1177/003591575805101014.
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本文引用的文献
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Cobalt, copper and molybdenum in the nutrition of animals and plants.动植物营养中的钴、铜和钼。
Physiol Rev. 1952 Jan;32(1):66-121. doi: 10.1152/physrev.1952.32.1.66.
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[Nervous manifestations of porphyria].
Sem Hop. 1950 Sep 2;26(65):3404-23.
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Congenital galactosaemia and mental health.先天性半乳糖血症与心理健康。
Lancet. 1958 Feb 1;1(7014):267-8. doi: 10.1016/s0140-6736(58)90957-7.
4
A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.一种可能为遗传性的疾病，其特征为严重智力缺陷和氨基酸代谢持续明显异常。
Lancet. 1958 Jan 25;1(7013):182-7. doi: 10.1016/s0140-6736(58)90666-4.
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Porphyria; a South African screening experiment.卟啉病；一项南非筛查实验。
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Laboratory diagnosis of congenital galactosaemia at birth.出生时先天性半乳糖血症的实验室诊断。
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7
The treatment of acute porphyria with chelating agents: a report of 21 cases.用螯合剂治疗急性卟啉病：21例报告。
Ann Intern Med. 1957 Nov;47(5):889-99. doi: 10.7326/0003-4819-47-5-889.
8
Phenylketonuria with normal intelligence and Gowers' muscular dystrophy.智力正常的苯丙酮尿症与高尔斯肌营养不良症。
Arch Dis Child. 1957 Aug;32(164):313-7. doi: 10.1136/adc.32.164.313.
9
Intermittent aldosteronism in periodic paralysis; dependence of attacks on retention of sodium, and failure to induce attacks by restriction of dietary sodium.周期性麻痹中的间歇性醛固酮增多症；发作对钠潴留的依赖性，以及通过限制饮食中的钠来诱发发作的失败。
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10
Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.通过苯丙氨酸耐量试验检测苯丙酮尿症杂合子携带者。
Nature. 1956 Dec 1;178(4544):1239-40. doi: 10.1038/1781239a0.
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