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 *

159 related articles for article (PubMed ID: 7439195)

  • 1. Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of age.
    Langenbeck U; Behbehani A; Mench-Hoinowski A; Petersen M
    Eur J Pediatr; 1980 Aug; 134(2):115-8. PubMed ID: 7439195
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants.
    Rey F; Pellié C; Sivy M; Blandin-Savoja F; Rey J; Frézal J
    Pediatr Res; 1974 May; 8(5):540-5. PubMed ID: 4151091
    [No Abstract]   [Full Text] [Related]  

  • 3. [Relations between serum phenylalanine level and phenylpyruvate and o-hydroxyphenylacetate in urine of patients with phenylketonuria, treated by diet].
    Zelnícek E; Podhradská O; Sláma J
    Bratisl Lek Listy; 1971; 55(1):63-9. PubMed ID: 5549026
    [No Abstract]   [Full Text] [Related]  

  • 4. [Relationship of urinary phenylpyruvate and o-hydroxyphenylacetate on serum phenylalanine level in patients with phenylketonuria treated by diet].
    Zelnícek E; Sláma J; Podhradská O
    Cas Lek Cesk; 1975 Apr; 114(17):518-21. PubMed ID: 1131843
    [No Abstract]   [Full Text] [Related]  

  • 5. Phenylpyruvate and o-hydroxyphenylacetate in phenylketonuric urine.
    Zelníćek E; Sláma J
    Clin Chim Acta; 1971 Dec; 35(2):496-7. PubMed ID: 5125336
    [No Abstract]   [Full Text] [Related]  

  • 6. [Phenylpyruvate and o-hydroxyphenylacetate in the urine of phenylketonurics treated by dietary measures].
    Zelnícek E; Podhradská O; Sláma J
    Z Kinderheilkd; 1970; 108(3):258-64. PubMed ID: 5475034
    [No Abstract]   [Full Text] [Related]  

  • 7. Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load.
    Rampini S; Völlmin JA; Bosshard HR; Müller M; Curtius HC
    Pediatr Res; 1974 Jul; 8(7):704-9. PubMed ID: 4837567
    [No Abstract]   [Full Text] [Related]  

  • 8. Results of loading doses of aspartame by two phenylketonuric (PKU) children compared with two normal children.
    Koch R; Schaeffler G; Shaw NF
    J Toxicol Environ Health; 1976 Nov; 2(2):459-69. PubMed ID: 1011297
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Urinary excretion of aromatic acids in hyperphenylalaninemic states: response to a protein challenge.
    Koepp P; Scholtyssek M; Plettner C
    Eur J Pediatr; 1978 Apr; 127(4):269-78. PubMed ID: 668711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aromatic acid excretion in classical phenylketonuria and hyperphenylalaninemic variants.
    Koepp P; Hoffmann B
    Helv Paediatr Acta; 1974 Nov; 29(5):489-98. PubMed ID: 4452644
    [No Abstract]   [Full Text] [Related]  

  • 11. Influence of the phenylalanine dose on the aromatic acid excretion in phenylketonuric heterozygotes and controls after oral loading.
    Dahmann G; Olek K; Pravitz A; Wardenbach P
    Eur J Pediatr; 1978 Oct; 129(3):191-5. PubMed ID: 699924
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenylalanine o-hydroxy-phenylacetic acid phenylpyruvic acid equals phenylketonuric diagnosis. A report of studies made on 77 students in schools for mentally retarded.
    VEAL AR
    Am J Med Technol; 1961; 27():191-6. PubMed ID: 13780514
    [No Abstract]   [Full Text] [Related]  

  • 13. Statistical evaluation of a new method to detect carriers of phenylketonuria.
    Minami R; Olek K; Wardenbach P
    Humangenetik; 1975 Sep; 29(2):151-4. PubMed ID: 1236833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aromatic acid excretion in phenylketonuria. Analysis of the unconjugated aromatic acids derived from phenylalanine.
    Blau K
    Clin Chim Acta; 1970 Jan; 27(1):5-18. PubMed ID: 5412612
    [No Abstract]   [Full Text] [Related]  

  • 15. Gas chromatographic analysis of abnormal urinary organic acids in phenylketonuria.
    Hsiao KJ; Hung SH; Wu SJ; Yeh SF
    Taiwan Yi Xue Hui Za Zhi; 1985 Nov; 84(11):1240-50. PubMed ID: 3868699
    [No Abstract]   [Full Text] [Related]  

  • 16. Study on urinary metabolic profile of phenylketonuria by micellar electrokinetic capillary chromatography with dual electrochemical detection--potential clinical application in fast diagnosis of phenylketonuria.
    Zhang D; Li W; Zhang J; Tang W; Qian C; Feng M; Chu Q; Ye J
    Anal Chim Acta; 2011 May; 694(1-2):61-6. PubMed ID: 21565303
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Diet in phenylketonuria].
    Richardet JM; Brissaud HE; Raynaud J; Repesse G; Galli J
    Arch Fr Pediatr; 1969; 26(7):791-807. PubMed ID: 5355253
    [No Abstract]   [Full Text] [Related]  

  • 19. A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.
    Langenbeck U; Behbehani A; Mench-Hoinowski A
    J Inherit Metab Dis; 1992; 15(1):136-44. PubMed ID: 1583868
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical phenylketonuria with borderline or normal intelligence.
    Hsia DY; O'Flynn ME; Berman JL
    Am J Dis Child; 1968 Aug; 116(2):143-57. PubMed ID: 5659290
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.