• 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

Incidence of phenylketonuria (PKU) in Iran.

作者信息

Farhud D D, Kabiri M

出版信息

Indian J Pediatr. 1982 Sep-Oct;49(400):685-8. doi: 10.1007/BF02752654.

DOI:10.1007/BF02752654
PMID:7188192
Abstract
摘要

相似文献

1
Incidence of phenylketonuria (PKU) in Iran.
Indian J Pediatr. 1982 Sep-Oct;49(400):685-8. doi: 10.1007/BF02752654.
2
Neonatal screening for phenylketonuria. II. Age dependence of initial phenylalanine in infants with PKU.苯丙酮尿症的新生儿筛查。II. 苯丙酮尿症患儿初始苯丙氨酸水平的年龄依赖性。
Pediatrics. 1974 Mar;53(3):353-7.
3
[15 years of national screening for phenylketonuria in The Netherlands; 4th Report of the National Commission for Management of Phenylketonuria].
Ned Tijdschr Geneeskd. 1990 Dec 29;134(52):2533-6.
4
Phenylketonuria variants in Ontario.安大略省的苯丙酮尿症变体
Can Med Assoc J. 1976 Sep 18;115(6):509-12.
5
The Effects of Breastfeeding in Infants With Phenylketonuria.苯丙酮尿症婴儿母乳喂养的影响
J Pediatr Nurs. 2018 Jan-Feb;38:27-32. doi: 10.1016/j.pedn.2017.10.009. Epub 2017 Oct 19.
6
A survey for the incidence of phenylketonuria in Guangdong, China.中国广东苯丙酮尿症发病率调查。
Southeast Asian J Trop Med Public Health. 2003;34 Suppl 3:185.
7
Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuria.成年苯丙酮尿症患者合并症的患病率。
Mol Genet Metab. 2018 Nov;125(3):228-234. doi: 10.1016/j.ymgme.2018.09.006. Epub 2018 Sep 12.
8
[Early detection of phenylketonuria in the Netherlands, 1977-1979. 2d report of the National Care Commission on Phenylketonuria].
Ned Tijdschr Geneeskd. 1981 Dec 26;125(52):2135-40.
9
[Routine early diagnosis of phenylketonuria using the Guthrie test in the GDR].
Dtsch Gesundheitsw. 1971 Oct 14;26(42):1977-80.
10
[Did the change of technique of screening investigations influence on improvement of test credibility in recognizing and differentiating diagnostics of hiperphenylalaninemias?].[筛查检查技术的改变是否对提高高苯丙氨酸血症诊断识别和鉴别诊断的检测可信度有影响？]
Przegl Lek. 2009;66(1-2):11-3.

引用本文的文献

1
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review.伊朗高苯丙氨酸血症患者中 PAH、QDPR、PTS 和 PCD 基因致病变异的综合研究：系统评价。
Hum Hered. 2023;88(1):8-17. doi: 10.1159/000529037. Epub 2023 Jan 16.
2
Phenylketonuria screening in Iranian newborns: a systematic review and meta-analysis.伊朗新生儿苯丙酮尿症筛查：系统评价和荟萃分析。
BMC Pediatr. 2020 Jul 24;20(1):352. doi: 10.1186/s12887-020-02230-6.
3
Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

本文引用的文献

1
A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.一种用于在大量新生儿群体中检测苯丙酮尿症的简易苯丙氨酸方法。
Pediatrics. 1963 Sep;32:338-43.
2
A new cofactor required for the enzymatic conversion of phenylalanine to tyrosine.苯丙氨酸酶促转化为酪氨酸所需的一种新辅助因子。
J Biol Chem. 1958 Feb;230(2):931-9.
3
A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia).
Lancet. 1968 Jan 20;1(7534):114-7. doi: 10.1016/s0140-6736(68)92722-0.
基于新生儿筛查项目数据的经典苯丙酮尿症全球患病率：系统评价与荟萃分析
Clin Exp Pediatr. 2020 Feb;63(2):34-43. doi: 10.3345/kjp.2019.00465. Epub 2020 Feb 6.
4
The Prevalence of Phenylketonuria in Arab Countries, Turkey, and Iran: A Systematic Review.阿拉伯国家、土耳其和伊朗苯丙酮尿症的流行情况：系统评价。
Biomed Res Int. 2018 Apr 18;2018:7697210. doi: 10.1155/2018/7697210. eCollection 2018.
5
Incidence of Neonatal Hyperphenylalaninemia Based on High-performance Liquid Chromatography Confirmatory Technique in Mazandaran Province, Northern Iran (2007-2015).基于高效液相色谱确证技术的伊朗北部马赞德兰省新生儿高苯丙氨酸血症发病率（2007 - 2015年）
Int J Prev Med. 2017 Nov 7;8:93. doi: 10.4103/ijpvm.IJPVM_24_17. eCollection 2017.
6
Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report.伊朗苯丙酮尿症家族中PAH基因新突变的鉴定：病例报告
Iran J Public Health. 2017 Apr;46(4):560-564.
7
Prevalence of classical phenylketonuria in mentally retarded individuals in Iran.伊朗智障人群中经典苯丙酮尿症的流行率。
J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S283-7. doi: 10.1007/s10545-009-1222-9. Epub 2009 Sep 19.
4
On the population genetics of phenylketonuria in the G.D.R.
Hum Genet. 1976 Jan 28;31(1):107-11. doi: 10.1007/BF00270406.
5
Incidence and distribution of pku-cases in Denmark.
Ir Med J. 1976 Sep 30;69(15):395-6.
6
The gene frequency of phenylketonuria among Thai population -- a preliminary report.
J Med Assoc Thai. 1976 Aug;59(8):359-62.
7
Phenylketonuria screening in Scotland 1965-1977.
Health Bull (Edinb). 1978 Sep;36(5):227-9.
8
Genetic screening of the newborn in Australia.
Med J Aust. 1977 Oct 22;2(17):579. doi: 10.5694/j.1326-5377.1977.tb114653.x.
9
Genetics and biochemistry of the phenylketonuria-present state.
Hum Genet. 1979 Oct 2;51(3):241-5. doi: 10.1007/BF00283389.