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 *

189 related articles for article (PubMed ID: 4417439)

  • 1. Thin-layer chromatographic screening of amino acids in plasma and urine of newborns.
    Century B; Vorkink WP; Natelson S
    Clin Chem; 1974 Nov; 20(11):1446-50. PubMed ID: 4417439
    [No Abstract]   [Full Text] [Related]  

  • 2. A survey of inborn errors of amino acid metabolism and transport in man.
    Wellner D; Meister A
    Annu Rev Biochem; 1981; 50():911-68. PubMed ID: 6791581
    [No Abstract]   [Full Text] [Related]  

  • 3. Problems in screening infants for defects of amino acid metabolism.
    Jackson SH
    Clin Biochem; 1973 Mar; 6(1):15-21. PubMed ID: 4121648
    [No Abstract]   [Full Text] [Related]  

  • 4. [The inborn errors of metabolism of amino acids].
    Tomaszewski L
    Postepy Biochem; 1973; 19(1):91-122. PubMed ID: 4697972
    [No Abstract]   [Full Text] [Related]  

  • 5. A simple screening method for detecting isovalerylglycine in urine patients with isovaleric acidemia.
    Ando T; Nyhan WL
    Clin Chem; 1970 May; 16(5):420-2. PubMed ID: 5443766
    [No Abstract]   [Full Text] [Related]  

  • 6. [Diagnostic methods for the detection of amino acid metabolism disorders].
    Lutz P
    Monatsschr Kinderheilkd (1902); 1973 May; 121(5):184-9. PubMed ID: 4197345
    [No Abstract]   [Full Text] [Related]  

  • 7. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose.
    Vercaemst R; Blaton V; Lievens-Taveirne J; Peeters H
    Acta Paediatr Belg; 1973; 27(5):334-47. PubMed ID: 4779694
    [No Abstract]   [Full Text] [Related]  

  • 8. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism].
    Charpentier C; Lemonnier A
    Ann Biol Clin (Paris); 1969; 27(5):297-323. PubMed ID: 4897889
    [No Abstract]   [Full Text] [Related]  

  • 9. A sensitive chromatographic technique for screening of amino acid metabolic defects in the newborn.
    Lato M; Rufini S; Ghebregzabher M; Ciuffini G; Mezzetti T
    Clin Chim Acta; 1974 Jun; 53(3):273-80. PubMed ID: 4858769
    [No Abstract]   [Full Text] [Related]  

  • 10. [Amino acid metabolism pathology in the convulsive syndrome in young children].
    Alimov IIu; Iur'eva EA; Marchenko ZM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1497-500. PubMed ID: 4660427
    [No Abstract]   [Full Text] [Related]  

  • 11. [Chromatographic investigation of free amino acids of the heart, kidneys and brain in experimental myocarditis].
    Andreeva LA
    Biull Eksp Biol Med; 1966 Nov; 31(11):52-3. PubMed ID: 6005449
    [No Abstract]   [Full Text] [Related]  

  • 12. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies].
    Segni G
    Minerva Nipiol; 1970; 20(4):83-110. PubMed ID: 4396023
    [No Abstract]   [Full Text] [Related]  

  • 13. Recent advances in the early detection and treatment of inborn errors with brain damage.
    Bickel H
    Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066
    [No Abstract]   [Full Text] [Related]  

  • 14. Application of a thin-layer chromatography microtechnique for the screening of aminoacidurias in 3,165 Chinese newborns.
    Wang TR
    Taiwan Yi Xue Hui Za Zhi; 1984 Sep; 83(9):869-78. PubMed ID: 6596395
    [No Abstract]   [Full Text] [Related]  

  • 15. [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]  

  • 16. Genetic screening.
    Levy HL
    Adv Hum Genet; 1973; 4():1-104. PubMed ID: 4593296
    [No Abstract]   [Full Text] [Related]  

  • 17. Simplified thin layer chromatography screening test for detection of important hyperaminoacidemias.
    Kraffczyk F; Helger R; Lang H
    Clin Chim Acta; 1971 Feb; 31(2):489-91. PubMed ID: 5573693
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. [Lethal familial neonatal ketotic hyperammonemia].
    Pauli A; Huguet J; Rollet M; Cousin J; Farriaux JP; Fournier A; Navarro J; Cathelineau L; Aymard P; Saudubray JM; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):699-712. PubMed ID: 4644460
    [No Abstract]   [Full Text] [Related]  

  • 20. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities.
    Wadman SK
    Acta Univ Carol Med Monogr; 1977; (77 Pt 1):49-69. PubMed ID: 615451
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.