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 *

177 related articles for article (PubMed ID: 5053206)

  • 1. [Detection of heterozygotes of typical phenylketonuria].
    Farriaux JP; Delabre M
    Arch Fr Pediatr; 1972 Apr; 29(4):365-72. PubMed ID: 5053206
    [No Abstract]   [Full Text] [Related]  

  • 2. [A new method of detection of heterozygotes in phenylpyruvic oligophrenia].
    Mamelle N; Mamelle JC; Site J; Quincy C; Later R; Masson E; Moreau P; François R
    Rev Eur Etud Clin Biol; 1971 Apr; 16(4):342-51. PubMed ID: 5564546
    [No Abstract]   [Full Text] [Related]  

  • 3. [Intravenous loading of L-phenylalanine: detection of heterozygotes in phenylketonuria].
    Lambert J; Viailhet M; Monot C; Lepoire E; Baradel J; Nabet P; Martin J; Pierson M
    C R Seances Soc Biol Fil; 1973; 167(3):502-8. PubMed ID: 4785089
    [No Abstract]   [Full Text] [Related]  

  • 4. Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.
    Cunningham GC; Day RW; Berman JL; Hsia DY
    Am J Dis Child; 1969 Jun; 117(6):626-35. PubMed ID: 5771502
    [No Abstract]   [Full Text] [Related]  

  • 5. [Intravenous phenylalanine loading test in normal subjects and the parents of phenylketonuretics].
    Badinand A; François R; Site J; Quincy C; Mamelle N; Masson E; Later R
    C R Seances Soc Biol Fil; 1968; 162(8):1525-8. PubMed ID: 4238174
    [No Abstract]   [Full Text] [Related]  

  • 6. Screening for PKU heterozygosity in bipolar affectively ill patients.
    Targum SD; Gershon ES; Shen RS; Abell CW
    Biol Psychiatry; 1979 Aug; 14(4):651-5. PubMed ID: 486619
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of heterozygotes for phenylketonuria. Total body phenylalanine clearance and concentrations of phenylalanine and tyrosine in the plasms of fasting subjects compared.
    Jagenburg R; Regårdh CG; Rödjer S
    Clin Chem; 1977 Sep; 23(9):1654-60. PubMed ID: 890909
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Method of detection of heterozygotic carrier state in phenylketonuria].
    Baikov AD; Sitnichenko EI
    Lab Delo; 1973; 5():293-5. PubMed ID: 4129158
    [No Abstract]   [Full Text] [Related]  

  • 9. [Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests].
    Barbesier J; Boisse J; Charpentier C; Lemonnier A; Mozziconacci P; Saudubray JM
    Presse Med (1893); 1971 Feb; 79(9):395-7. PubMed ID: 5546799
    [No Abstract]   [Full Text] [Related]  

  • 10. Quantitative analysis of phenylalanine metabolites in urine to detect heterozygotes of phenylketonuria.
    Olek K; Oyanagi K; Wardenbach P
    Humangenetik; 1974 Apr; 22(1):85-8. PubMed ID: 4837293
    [No Abstract]   [Full Text] [Related]  

  • 11. Contribution to the problems of determining heterozygotes in phenylketonuria by the biochemical and electroencephalographic method.
    Cechák P; Rákosníková M
    Acta Univ Carol Med Monogr; 1977; (79 Pt 3):57-64. PubMed ID: 615484
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of phenylketonuric heterozygotes.
    Jackson SH; Hanley WB; Gero T; Gosse GD
    Clin Chem; 1971 Jun; 17(6):538-43. PubMed ID: 5103385
    [No Abstract]   [Full Text] [Related]  

  • 13. [Intracellular concentration of phenylalanine, tyrosine and alpha-amino butyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals (author's transl)].
    Thalhammer O; Pollak A; Lubec G; Königshofer H
    Klin Padiatr; 1980 Nov; 192(6):608-12. PubMed ID: 7194402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenylketonuria: a family study.
    Crosby PF; Navarro A; Matos ML
    Bol Asoc Med P R; 1969 Apr; 61(4):133-7. PubMed ID: 5255738
    [No Abstract]   [Full Text] [Related]  

  • 15. [Heterozygote identification in phenylketonuria].
    Rampini S; Anders PW; Curtius HC; Marthaler T
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1968; 43(3-4):suppl 102-3. PubMed ID: 5761621
    [No Abstract]   [Full Text] [Related]  

  • 16. Detection of heterozygotes for phenylketonuria by column chromatography and discriminatory analysis.
    Rampini S; Anders PW; Curtius HC; Marthaler T
    Pediatr Res; 1969 Jul; 3(4):287-97. PubMed ID: 5807058
    [No Abstract]   [Full Text] [Related]  

  • 17. Discriminant analysis for detection of phenylketonuric heterozygotes.
    Christian BG
    Soc Biol; 1971 Mar; 18(1):64-72. PubMed ID: 5580588
    [No Abstract]   [Full Text] [Related]  

  • 18. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

  • 19. [Maternal phenylketonuria].
    Rittinger O; Plöchl E; Jarosch E
    Padiatr Padol; 1984; 19(1):87-92. PubMed ID: 6701000
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mass screening of phenylketonuria. Report on a screening center (October 1967-December 1968)].
    Barbesier J; Boisse J; Charpentier C; Lemonnier A; Mozziconacci P
    Presse Med (1893); 1969 Sep; 77(37):1279-82. PubMed ID: 4897489
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.