These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 7901023)

  • 1. Biochemical control, genetic analysis and magnetic resonance imaging in patients with phenylketonuria.
    Walter JH; Tyfield LA; Holton JB; Johnson C
    Eur J Pediatr; 1993 Oct; 152(10):822-7. PubMed ID: 7901023
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Magnetic resonance imaging of the brain in phenylketonuria.
    Cleary MA; Walter JH; Wraith JE; Jenkins JP; Alani SM; Tyler K; Whittle D
    Lancet; 1994 Jul; 344(8915):87-90. PubMed ID: 7912392
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Magnetic resonance imaging of the brain in phenylketonuria].
    Izumi M; Yamazaki H; Nakabayashi H; Owada M
    No To Hattatsu; 2006 Jan; 38(1):27-31. PubMed ID: 16447793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria.
    Güttler F; Ledley FD; Lidsky AS; DiLella AG; Sullivan SE; Woo SL
    J Pediatr; 1987 Jan; 110(1):68-71. PubMed ID: 2878985
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Blood-brain barrier phenylalanine transport and individual vulnerability in phenylketonuria.
    Möller HE; Weglage J; Wiedermann D; Ullrich K
    J Cereb Blood Flow Metab; 1998 Nov; 18(11):1184-91. PubMed ID: 9809507
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change.
    Cleary MA; Walter JH; Wraith JE; White F; Tyler K; Jenkins JP
    J Pediatr; 1995 Aug; 127(2):251-5. PubMed ID: 7636650
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of treated and untreated phenylketonuria in one family.
    Tyfield LA; Meredith AL; Osborn MJ; Primavesi R; Chambers TL; Holton JB; Harper PS
    J Med Genet; 1990 Sep; 27(9):564-8. PubMed ID: 1977916
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus.
    Berthelon M; Caillaud C; Rey F; Labrune P; Melle D; Feingold J; Frézal J; Briard ML; Farriaux JP; Guibaud P
    Hum Genet; 1991 Feb; 86(4):355-8. PubMed ID: 1671847
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.
    Svensson E; von Döbeln U; Hagenfeldt L
    Hum Genet; 1991 May; 87(1):11-7. PubMed ID: 1674714
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Correlation between genotypes and biochemical phenotypes of phenylalanine hydroxylase in patients with phenylketonuria].
    Shu JB; Meng YT; Dang LH; Fu BJ; Song L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):635-41. PubMed ID: 23225039
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brain imaging and proton magnetic resonance spectroscopy in patients with phenylketonuria.
    Möller HE; Weglage J; Bick U; Wiedermann D; Feldmann R; Ullrich K
    Pediatrics; 2003 Dec; 112(6 Pt 2):1580-3. PubMed ID: 14654669
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population.
    Lichter-Konecki U; Schlotter M; Yaylak C; Ozgüç M; Coskun T; Ozalp I; Wendel U; Batzler U; Trefz FK; Konecki D
    Hum Genet; 1989 Mar; 81(4):373-6. PubMed ID: 2564839
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.
    Dianzani I; Devoto M; Camaschella C; Saglio G; Ferrero GB; Cerone R; Romano C; Romeo G; Giovannini M; Riva E
    Hum Genet; 1990 Nov; 86(1):69-72. PubMed ID: 1979309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distributions of phenylalanine hydroxylase mutations and haplotypes in Lithuanian phenylketonuria patients.
    Kucinskas V; Jurgelevicius V; Cimbalistiene L; Holmgren G
    Hum Hered; 1994; 44(2):110-3. PubMed ID: 8188310
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diffusion-weighted MR imaging in patients with phenylketonuria: relationship between serum phenylalanine levels and ADC values in cerebral white matter.
    Kono K; Okano Y; Nakayama K; Hase Y; Minamikawa S; Ozawa N; Yokote H; Inoue Y
    Radiology; 2005 Aug; 236(2):630-6. PubMed ID: 16040919
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
    Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
    J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Blood-brain phenylalanine relationships in persons with phenylketonuria.
    Koch R; Moats R; Guttler F; Guldberg P; Nelson M
    Pediatrics; 2000 Nov; 106(5):1093-6. PubMed ID: 11061780
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis of RFLP haplotypes and point mutations at the phenylalanine hydroxylase (PAH) locus in PKU families from north China].
    Fang B
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):46-50. PubMed ID: 1350519
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.
    Konecki DS; Lichter-Konecki U
    Hum Genet; 1991 Aug; 87(4):377-88. PubMed ID: 1679029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.
    Chakraborty R; Lidsky AS; Daiger SP; Güttler F; Sullivan S; Dilella AG; Woo SL
    Hum Genet; 1987 May; 76(1):40-6. PubMed ID: 2883110
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.