• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Dietary treatment of homocystinuria.

作者信息

Komrower G M, Lambert A M, Cusworth D C, Westall R G

出版信息

Arch Dis Child. 1966 Dec;41(220):666-71. doi: 10.1136/adc.41.220.666.

DOI:10.1136/adc.41.220.666
PMID:5954709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2019674/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb5f/2019674/84da1fbeca27/archdisch01573-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb5f/2019674/84da1fbeca27/archdisch01573-0100-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb5f/2019674/84da1fbeca27/archdisch01573-0100-a.jpg

相似文献

1
Dietary treatment of homocystinuria.同型胱氨酸尿症的饮食治疗。
Arch Dis Child. 1966 Dec;41(220):666-71. doi: 10.1136/adc.41.220.666.
2
Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor.
Lancet. 1968 Aug 31;2(7566):474-8. doi: 10.1016/s0140-6736(68)90646-6.
3
Treatment of homocystinuria.同型胱氨酸尿症的治疗。
Arch Dis Child. 1967 Oct;42(225):514-20. doi: 10.1136/adc.42.225.514.
4
Homocystinuria. Trial treatment of a 5-year old severely retarded child with a natural diet low in methionine.
Am J Dis Child. 1967 Jan;113(1):95-7.
5
Dietary treatment of homocystinuria.
Am J Dis Child. 1967 Jan;113(1):98-100. doi: 10.1001/archpedi.1967.02090160148022.
6
Some theoretical considerations in the treatment of homocystinuria.
Am J Dis Child. 1967 Jan;113(1):101-2. doi: 10.1001/archpedi.1967.02090160151023.
7
Nonketotic hyperglycinemia: an in vitro study of the glycine-serine conversion in liver of three patients and the effect of dietary methionine.非酮症高甘氨酸血症：三名患者肝脏中甘氨酸-丝氨酸转化的体外研究及膳食蛋氨酸的影响。
Pediatr Res. 1970 May;4(3):238-43. doi: 10.1203/00006450-197005000-00002.
8
[Dietetics in hereditary enzyme deficiencies].[遗传性酶缺乏症中的饮食学]
Sem Hop. 1970 Feb 26;46(10):653-9.
9
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。
Pediatr Res. 1968 May;2(3):149-60. doi: 10.1203/00006450-196805000-00001.
10
Dietary treatment of inborn errors of amino acid and carbohydrate metabolism.氨基酸和碳水化合物代谢先天性疾病的饮食治疗
Bibl Nutr Dieta. 1973(18):181-201. doi: 10.1159/000393052.

引用本文的文献

1
Paracetamol toxicity in classic homocystinuria: Effect of -acetylcysteine on total homocysteine.经典型同型胱氨酸尿症中的对乙酰氨基酚毒性：N-乙酰半胱氨酸对总同型半胱氨酸的影响
JIMD Rep. 2023 Mar 3;64(3):238-245. doi: 10.1002/jmd2.12363. eCollection 2023 May.
2
Interplay of Enzyme Therapy and Dietary Management of Murine Homocystinuria.酶治疗与饮食管理在治疗鼠同型胱氨酸尿症中的相互作用。
Nutrients. 2020 Sep 22;12(9):2895. doi: 10.3390/nu12092895.
3
The effectiveness of correcting abnormal metabolic profiles.纠正异常代谢谱的效果。

本文引用的文献

1
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.
2
PROTEIN AND AMINO ACID REQUIREMENTS OF INFANTS AND CHILDREN.婴幼儿的蛋白质和氨基酸需求
Nutr Abstr Rev. 1965 Jan;35:1-13.
3
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。
J Inherit Metab Dis. 2020 Jan;43(1):2-13. doi: 10.1002/jimd.12139. Epub 2019 Jul 17.
4
Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria.酶替代疗法改善了小鼠同型胱氨酸尿症的多种症状。
Mol Ther. 2018 Mar 7;26(3):834-844. doi: 10.1016/j.ymthe.2017.12.014. Epub 2017 Dec 19.
5
International Union of Basic and Clinical Pharmacology. CII: Pharmacological Modulation of HS Levels: HS Donors and HS Biosynthesis Inhibitors.国际基础与临床药理学联合会。CII：硫酸乙酰肝素水平的药理学调节：硫酸乙酰肝素供体和硫酸乙酰肝素生物合成抑制剂。
Pharmacol Rev. 2017 Oct;69(4):497-564. doi: 10.1124/pr.117.014050.
6
Enzyme replacement prevents neonatal death, liver damage, and osteoporosis in murine homocystinuria.酶替代疗法可预防小鼠同型胱氨酸尿症中的新生儿死亡、肝损伤和骨质疏松症。
FASEB J. 2017 Dec;31(12):5495-5506. doi: 10.1096/fj.201700565R. Epub 2017 Aug 16.
7
Cystathionine β-synthase deficiency: Of mice and men.胱硫醚β-合酶缺乏症：小鼠与人类
Mol Genet Metab. 2017 Jul;121(3):199-205. doi: 10.1016/j.ymgme.2017.05.011. Epub 2017 May 19.
8
Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.胱硫醚β-合酶缺乏症的诊断与管理指南。
J Inherit Metab Dis. 2017 Jan;40(1):49-74. doi: 10.1007/s10545-016-9979-0. Epub 2016 Oct 24.
9
Enzyme replacement with PEGylated cystathionine β-synthase ameliorates homocystinuria in murine model.用聚乙二醇化胱硫醚β-合酶进行酶替代可改善小鼠模型中的同型胱氨酸尿症。
J Clin Invest. 2016 Jun 1;126(6):2372-84. doi: 10.1172/JCI85396. Epub 2016 May 16.
10
The effect of dietary modulation of sulfur amino acids on cystathionine β synthase-deficient mice.膳食调节含硫氨基酸对胱硫醚β合酶缺陷小鼠的影响。
Ann N Y Acad Sci. 2016 Jan;1363(1):80-90. doi: 10.1111/nyas.12967. Epub 2015 Nov 24.
Science. 1964 Nov 6;146(3645):785-7. doi: 10.1126/science.146.3645.785.
4
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。
Pediatrics. 1964 Mar;33:413-20.
5
HOMOCYSTINURIA, THROMBOSIS, AND THE BLOOD-PLATELETS.
Lancet. 1964 Apr 4;1(7336):745-6. doi: 10.1016/s0140-6736(64)92852-1.
6
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.
7
HOMOCYSTINURIA.同型胱氨酸尿症
Proc R Soc Med. 1963 Nov;56(11):996-7. doi: 10.1177/003591576305601127.
8
DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).枫糖尿症（支链酮酸尿症）患儿的饮食治疗
Arch Dis Child. 1963 Oct;38(201):485-91. doi: 10.1136/adc.38.201.485.
9
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.
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.