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Journal Abstract Search

177 related items for PubMed ID: 33625639

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  • 3. Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations.
    Alibakhshi R, Moradi K, Mohebbi Z, Ghadiri K.
    Metab Brain Dis; 2014 Mar; 29(1):131-8. PubMed ID: 24048906
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  • 6. Mutational landscape of phenylketonuria in Iran.
    Ajami N, Soleimani A, Jafarzadeh-Esfehani R, Hasanpour M, Rashid Shomali R, Abbaszadegan MR.
    J Cell Mol Med; 2023 Sep; 27(17):2457-2466. PubMed ID: 37525467
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  • 8. Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuria.
    Biglari A, Saffari F, Rashvand Z, Alizadeh S, Najafipour R, Sahmani M.
    Springerplus; 2015 Sep; 4():542. PubMed ID: 26413448
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  • 9. Frequency of PAH Mutations Among Classic Phenylketon Urea Patients in Mazandaran and Golestan Provinces, North of Iran.
    Hosseini E, Mousavi SS, Zamanfar D, Hashemi-Soteh SMB.
    Clin Lab; 2022 Jan 01; 68(1):. PubMed ID: 35023679
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  • 11. PREVALENCE OF PAH MUTATIONS IN GEORGIAN PKU PATIENTS COMPARED TO MOST FREQUENT PAH MUTATIONS IN EUROPEAN POPULATIONS.
    Agladze D, Iordanishvili S, Margvelashvili L, Kldiashvili E, Kvlividze O.
    Georgian Med News; 2020 Nov 01; (308):143-149. PubMed ID: 33395657
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  • 15. Phenylketonuria in Iranian population: a study in institutions for mentally retarded in Isfahan.
    Vallian S, Barahimi E, Moeini H.
    Mutat Res; 2003 May 15; 526(1-2):45-52. PubMed ID: 12714182
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  • 19. The molecular basis of phenylketonuria in Latvia.
    Pronina N, Giannattasio S, Lattanzio P, Lugovska R, Vevere P, Kornejeva A.
    Hum Mutat; 2003 Apr 15; 21(4):398-9. PubMed ID: 12655551
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  • 20. Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations.
    Dehghanian F, Silawi M, Tabei SM.
    Clin Lab; 2017 Feb 01; 63(2):295-300. PubMed ID: 28182360
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