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Treatment of homocystinuria with a low-methionine diet, supplemental cystine, and a methyl donor.

作者信息

Perry T L, Hansen S, Love D L, Crawford L E, Tischler B

出版信息

Lancet. 1968 Aug 31;2(7566):474-8. doi: 10.1016/s0140-6736(68)90646-6.

DOI:10.1016/s0140-6736(68)90646-6
PMID:4175242
Abstract
摘要

相似文献

1
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.
2
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.
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
Pyridoxine treatment in homocystinuria.同型胱氨酸尿症的维生素B6治疗
Lancet. 1967 Nov 25;2(7526):1151. doi: 10.1016/s0140-6736(67)90662-9.
5
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.
6
Homocystinuria with congenital/developmental cataract.伴有先天性/发育性白内障的同型胱氨酸尿症
Indian J Pediatr. 2000 Oct;67(10):725-8. doi: 10.1007/BF02723928.
7
Homocystinuria: the significance of its successful treatment.
Trans Ophthalmol Soc U K (1962). 1969;88:47-78.
8
[Homocystinuria: clinical picture, therapy and results in 8 patients].
Dtsch Med Wochenschr. 1973 Jul 6;98(27):1313-9. doi: 10.1055/s-0028-1107021.
9
Sulfur-containing amino acids in the plasma and urine of homocystinurics.同型胱氨酸尿症患者血浆和尿液中的含硫氨基酸。
Clin Chim Acta. 1967 Mar;15(3):409-20. doi: 10.1016/0009-8981(67)90005-8.
10
Homocystinuria: amino acid pattern of the liver.同型胱氨酸尿症:肝脏的氨基酸模式
Tohoku J Exp Med. 1967 Aug;92(4):325-32. doi: 10.1620/tjem.92.325.

引用本文的文献

1
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.
2
An indirect response model of homocysteine suppression by betaine: optimising the dosage regimen of betaine in homocystinuria.甜菜碱对同型半胱氨酸抑制的间接反应模型:优化高胱氨酸尿症中甜菜碱的给药方案。
Br J Clin Pharmacol. 2002 Aug;54(2):140-6. doi: 10.1046/j.1365-2125.2002.01620.x.
3
Homocystinuria with congenital/developmental cataract.
伴有先天性/发育性白内障的同型胱氨酸尿症
Indian J Pediatr. 2000 Oct;67(10):725-8. doi: 10.1007/BF02723928.
4
Homocystinuria (cystathionine synthase deficiency). Results of treatment in late-diagnosed patients.同型胱氨酸尿症(胱硫醚合成酶缺乏症)。晚诊断患者的治疗结果。
Eur J Pediatr. 1980 Dec;135(2):199-203. doi: 10.1007/BF00441642.
5
Decreased methionine synthesis in purine nucleoside-treated T and B lymphoblasts and reversal by homocysteine.嘌呤核苷处理的T和B淋巴母细胞中蛋氨酸合成减少及同型半胱氨酸的逆转作用
J Clin Invest. 1984 Oct;74(4):1262-8. doi: 10.1172/JCI111536.
6
Therapeutic problems of adolescent homocystinuria.青少年同型胱氨酸尿症的治疗问题
Proc R Soc Med. 1969 Sep;62(9):909-10. doi: 10.1177/003591576906200923.
7
Treatment of homocystinuria with pyridoxine. A preliminary study.用吡哆醇治疗同型胱氨酸尿症。一项初步研究。
Arch Dis Child. 1969 Jun;44(235):387-92. doi: 10.1136/adc.44.235.387.
8
Psychiatric and biochemical aspects of a case of homocystinuria.一例同型胱氨酸尿症的精神和生化方面
J Neurol Neurosurg Psychiatry. 1969 Apr;32(2):88-93. doi: 10.1136/jnnp.32.2.88.
9
Homocystinuria.同型胱氨酸尿症
Biochem J. 1969 Feb;111(3):1P-2P. doi: 10.1042/bj1110001p.
10
Homocystinuria. Report of two cases in siblings.
Indian J Pediatr. 1970 Jun;37(269):263-7. doi: 10.1007/BF02807272.