Literature DB >> 11999985

Incidence of phenylketonuria in Iran estimated from consanguineous marriages.

J Koochmeshgi1, A Bagheri, S M Hosseini-Mazinani.   

Abstract

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Year:  2002        PMID： 11999985     DOI： 10.1023/a:1015154321142

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

1.  Inherited metabolic disorders in Turkey.

Authors:  I Ozalp; T Coskun; S Tokol; G Demircin; E Mönch
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Phenylketonuria in Turkey, Ireland and west Scotland.

Authors:  L I Woolf
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

3.  Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage.

Authors:  L I Woolf; M S McBean; F M Woolf; S F Cahalane
Journal:  Ann Hum Genet       Date:  1975-05       Impact factor: 1.670
  3 in total
  15 in total

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Journal:  Metab Brain Dis       Date:  2018-04-03       Impact factor: 3.584

2.  Frequency of the VNTR-Polymorphisms at the PAH Gene in the Iranian Azeri Turkish Patients with Phenylketonuria.

Authors:  Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi
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3.  Association Between PAH Mutations and VNTR Alleles in the West Azerbaijani PKU Patients.

Authors:  Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi
Journal:  Maedica (Buchar)       Date:  2014-09

4.  Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes.

Authors:  Leo P Ten Kate; Marieke Teeuw; Lidewij Henneman; Martina C Cornel
Journal:  J Community Genet       Date:  2010-02-25

5.  Prevalence of classical phenylketonuria in mentally retarded individuals in Iran.

Authors:  N M Ghiasvand; A Aledavood; R Ghiasvand; F Seyedin Borojeny; A R Aledavood; S Seyed; W Miner; G R Saeb Taheri
Journal:  J Inherit Metab Dis       Date:  2009-09-19       Impact factor: 4.982

6.  Executive dysfunction in treated phenylketonuric patients.

Authors:  Bahare Azadi; Arshia Seddigh; Mehdi Tehrani-Doost; Javad Alaghband-Rad; Mahmoud Reza Ashrafi
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-02-16       Impact factor: 4.785

7.  Motor development skills of 1- to 4-year-old Iranian children with early treated phenylketonuria.

Authors:  Sepideh Nazi; Farzaneh Rohani; Firoozeh Sajedi; Akbar Biglarian; Arya Setoodeh
Journal:  JIMD Rep       Date:  2013-08-06

8.  Phenylketonuria in Portugal: Genotype-phenotype correlations using molecular, biochemical, and haplotypic analyses.

Authors:  Filipa Ferreira; Luísa Azevedo; Raquel Neiva; Carmen Sousa; Helena Fonseca; Ana Marcão; Hugo Rocha; Célia Carmona; Sónia Ramos; Anabela Bandeira; Esmeralda Martins; Teresa Campos; Esmeralda Rodrigues; Paula Garcia; Luísa Diogo; Ana Cristina Ferreira; Silvia Sequeira; Francisco Silva; Luísa Rodrigues; Ana Gaspar; Patrícia Janeiro; António Amorim; Laura Vilarinho
Journal:  Mol Genet Genomic Med       Date:  2021-01-19       Impact factor: 2.183

9.  Mutation analysis of the phenylalanine hydroxylase gene in Azerbaijani population, a report from West Azerbaijan province of Iran.

Authors:  Morteza Bagheri; Isa Abdi Rad; Nima Hosseini Jazani; Rasoul Zarrin; Ahad Ghazavi
Journal:  Iran J Basic Med Sci       Date:  2015-07       Impact factor: 2.699

10.  Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuria.

Authors:  Alireza Biglari; Fatemeh Saffari; Zahra Rashvand; Safarali Alizadeh; Reza Najafipour; Mehdi Sahmani
Journal:  Springerplus       Date:  2015-09-23
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