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Phenylketonuria revisited: treatment of adults with behavioural manifestations.

作者信息

Brunner R L, Brown E H, Berry H K

机构信息

Division of Basic Science Research, Children's Hospital Medical Center, Cincinnati, Ohio.

出版信息

J Inherit Metab Dis. 1987;10(2):171-3. doi: 10.1007/BF01800044.

DOI:10.1007/BF01800044
PMID:3116336
Abstract

Dietary treatment of three PKU patients with irreversible changes is described and elevated.

摘要

相似文献

1
Phenylketonuria revisited: treatment of adults with behavioural manifestations.
J Inherit Metab Dis. 1987;10(2):171-3. doi: 10.1007/BF01800044.
2
The use of a low phenylalanine diet in response to the challenging behaviour of a man with untreated phenylketonuria and profound learning disabilities.针对一名未经治疗的苯丙酮尿症且有严重学习障碍男子的攻击性行为,采用低苯丙氨酸饮食。
J Intellect Disabil Res. 1995 Dec;39 ( Pt 6):520-6. doi: 10.1111/j.1365-2788.1995.tb00572.x.
3
[Phenylketonuria--change in therapeutic strategies. Study of intellectual development and dietary compliance of young phenylketonuria patients].[苯丙酮尿症——治疗策略的改变。苯丙酮尿症患儿智力发育及饮食依从性研究]
Fortschr Med. 1993 Nov 10;111(31):485-8.
4
Social quotients of children with phenylketonuria before and after discontinuation of dietary therapy.苯丙酮尿症患儿停止饮食治疗前后的社交商数。
Am J Ment Defic. 1986 Jul;91(1):92-4.
5
[Phenylketonuria and its treatment in and beyond adolescence].
Internist (Berl). 1994 Mar;35(3):250-4.
6
Maternal phenylketonuria.母体苯丙酮尿症
Postgrad Med J. 1989;65 Suppl 2:S10-20.
7
The use of a low phenylalanine diet with amino acid supplement in the treatment of behavioural problems in a severely mentally retarded adult female with phenylketonuria.使用低苯丙氨酸饮食并补充氨基酸治疗一名患有苯丙酮尿症的重度智力迟钝成年女性的行为问题。
J Intellect Disabil Res. 1992 Apr;36 ( Pt 2):183-91. doi: 10.1111/j.1365-2788.1992.tb00494.x.
8
[Treatment of phenylketonuria: wish and reality].
Monatsschr Kinderheilkd. 1993 Aug;141(8):670-4.
9
Maternal PKU syndrome in an exceptional family with unexpected PKU.一个患有罕见苯丙酮尿症的特殊家庭中的母体苯丙酮尿症综合征
J Inherit Metab Dis. 1987;10(2):162-70. doi: 10.1007/BF01800043.
10
The management of phenylketonuria (PKU).苯丙酮尿症(PKU)的管理
Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:55-7.

引用本文的文献

1
[Singleton and twin pregnancies of PKU patients - individual variability of phenylalanine tolerance: experience of a single treatment center (Preliminary report)].[苯丙酮尿症患者的单胎和双胎妊娠——苯丙氨酸耐受性的个体差异:单一治疗中心的经验(初步报告)]
Dev Period Med. 2017;21(4):344-360. doi: 10.34763/devperiodmed.20172104.344360.
2
Insurance coverage of special foods needed in the treatment of phenylketonuria.苯丙酮尿症治疗所需特殊食品的保险覆盖范围。
Public Health Rep. 1993 Jan-Feb;108(1):60-5.
3
Improvements in behaviour and physical manifestations in previously untreated adults with phenylketonuria using a phenylalanine-restricted diet: a national survey.

本文引用的文献

1
Preliminary support for the oral administration of valine, isoleucine and leucine for phenylketonuria.关于口服缬氨酸、异亮氨酸和亮氨酸治疗苯丙酮尿症的初步支持。
Dev Med Child Neurol. 1985 Feb;27(1):33-9. doi: 10.1111/j.1469-8749.1985.tb04522.x.
2
Large doses of tryptophan and tyrosine as potential therapeutic alternative to dietary phenylalanine restriction in phenylketonuria.
Lancet. 1985 Jul 20;2(8447):150-1. doi: 10.1016/s0140-6736(85)90250-8.
采用低苯丙氨酸饮食对既往未治疗的苯丙酮尿症成年患者行为和身体表现的改善:一项全国性调查。
J Inherit Metab Dis. 1995;18(2):131-4. doi: 10.1007/BF00711747.