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 *

181 related articles for article (PubMed ID: 1112063)

  • 1. Detection of heterozygotes for phenylketonuria and hyperphenylaianinemia by gas-chromatographic analysis of aromatic acid excretion in urine.
    Koepp P; Hoffman B
    Clin Chim Acta; 1975 Feb; 58(3):215-21. PubMed ID: 1112063
    [No Abstract]   [Full Text] [Related]  

  • 2. [Phenylalanine metabolites in the urine after oral phenylalanine loading. Significance for the discrimination between classical phenylketonuria and variations of hyperphenylalaninemia (heterozygotes and homozygotes)].
    Koepp P
    Fortschr Med; 1977 Mar; 95(10):627-31. PubMed ID: 844759
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading test.
    Blitzer MG; Bailey-Wilson JE; Shapira E
    Clin Chim Acta; 1985 Dec; 153(2):137-42. PubMed ID: 4064343
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S; Skjelkvåle L
    Lakartidningen; 1974 Mar; 71(12):1166-7. PubMed ID: 4821497
    [No Abstract]   [Full Text] [Related]  

  • 5. Serum tyrosine within the first hour after an oral load of phenylalanine.
    Güttler F; Hansen G
    Scand J Clin Lab Invest; 1977 Dec; 37(8):717-21. PubMed ID: 601515
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria.
    Blau K; Summer GK; Newsome HC; Edwards CH
    Clin Chim Acta; 1973 May; 45(3):197-205. PubMed ID: 4708049
    [No Abstract]   [Full Text] [Related]  

  • 7. Gas-liquid chromatography of phenylalanine metabolites in urine and sera of hyperphenylalaninemic and phenylketonuric patients.
    Kitagawa T
    Clin Chem; 1974 Dec; 20(12):1543-7. PubMed ID: 4430132
    [No Abstract]   [Full Text] [Related]  

  • 8. The assessment of serum amino acids.
    Swallow WH; Carrell RW
    N Z Med J; 1970 Feb; 71(453):85-8. PubMed ID: 5267129
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Neonatal screening for inborn errors of amino acid metabolism.
    Levy HL
    Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646
    [No Abstract]   [Full Text] [Related]  

  • 11. [Value of the assay of urine ortho-hydroxyphenylacetic acid in hyperphenylalaninemia].
    Dhondt JL; Cartigny B; Farriaux JP
    Ann Biol Clin (Paris); 1974; 32(6):499-506. PubMed ID: 4468743
    [No Abstract]   [Full Text] [Related]  

  • 12. A rapid procedure for the determination of phenylalanine and tyrosine from blood filter paper specimens.
    Levy HL; Baullinger PC; Madigan PM
    Clin Chim Acta; 1971 Feb; 31(2):447-52. PubMed ID: 5573686
    [No Abstract]   [Full Text] [Related]  

  • 13. From the Clinical Conference St. Louis Children's Hospital. Phenylketonuria. Diagnostic and therapeutic dilemma.
    Kahn LI
    Clin Pediatr (Phila); 1970 May; 9(5):263-71. PubMed ID: 5445064
    [No Abstract]   [Full Text] [Related]  

  • 14. Effect of cotrimoxazole on the response to phenylalanine loading in man.
    Clin Chim Acta; 1976 Apr; 68(1):17-30. PubMed ID: 1261050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Problems in the biochemical detection of heterozygotes for phenylketonuria.
    Yakymyshyn LY; Reid DW; Campbell DJ
    Clin Biochem; 1972 Mar; 5(1):73-81. PubMed ID: 5022449
    [No Abstract]   [Full Text] [Related]  

  • 16. Rapid automated quantitation of isoleucine, leucine, tyrosine and phenylalanine from dried blood filter paper specimens.
    Qu Y; Miller JB; Slocum RH; Shapira E
    Clin Chim Acta; 1991 Dec; 203(2-3):191-7. PubMed ID: 1777980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [The problem in the differential diagnosis of various forms of hyperphenylalaninemia and in its diet therapy].
    Zammarchi E
    Minerva Pediatr; 1977 Apr; 29(12):873-7. PubMed ID: 559914
    [No Abstract]   [Full Text] [Related]  

  • 19. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].
    Menne F; Enzenauer J; Matz D
    Med Klin; 1976 Apr; 71(17):724-8. PubMed ID: 775276
    [No Abstract]   [Full Text] [Related]  

  • 20. Ion-exchange thin-layer chromatographic screening test for phenylketonuria and other aminoacidaemias.
    Kovács J
    Acta Paediatr Acad Sci Hung; 1973; 14(3):165-9. PubMed ID: 4785695
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.