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 *

105 related articles for article (PubMed ID: 405681)

  • 1. Serial study of the urinary metabolites in newborn children.
    Tănase I; Ciortoloman H; Grigorescu G; Popescu M
    Physiologie; 1977; 14(2):101-5. PubMed ID: 405681
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Aspects of the biochemistry of the urine in mental deficiency in children].
    Tănase I
    Physiologie; 1975; 12(3):211-4. PubMed ID: 812122
    [No Abstract]   [Full Text] [Related]  

  • 3. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles].
    Plöchl E
    Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107
    [No Abstract]   [Full Text] [Related]  

  • 4. [Excretion of amino acids, keto acids, pentoses and choline in cerebral anomalies in children].
    Tănase I
    Rev Roum Physiol; 1972; 9(6):471-8. PubMed ID: 4656903
    [No Abstract]   [Full Text] [Related]  

  • 5. [New types of congenital metabolic errors detected in newborn infants].
    Tănase Mogoş I; Boerescu J
    Physiologie; 1975; 12(4):27k-3. PubMed ID: 814559
    [No Abstract]   [Full Text] [Related]  

  • 6. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I; Ciortoloman H; Grigorescu G; Popescu M; Ankăr V
    Physiologie; 1978; 15(4):239-43. PubMed ID: 106407
    [No Abstract]   [Full Text] [Related]  

  • 7. [Screening of newborn infants for inborn errors of metabolism].
    Halvorsen S; Skjelkvåle L
    Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194
    [No Abstract]   [Full Text] [Related]  

  • 8. Screening for metabolic disorders among high risk infants and children.
    Berry HK
    Health Lab Sci; 1977 Jul; 14(3):183-93. PubMed ID: 141435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of inborn errors of metabolism.
    Boggs DE
    CRC Crit Rev Clin Lab Sci; 1971; 2(4):529-72. PubMed ID: 4257997
    [No Abstract]   [Full Text] [Related]  

  • 10. ["Atypical" metabolic forms of phenylketonuria (PKU) and leucinosis detected in newborn infants].
    Tănase I; Ciortoloman H; Popescu M; Grigorescu G; Ankăr V
    Physiologie; 1977; 14(4):257-61. PubMed ID: 413127
    [No Abstract]   [Full Text] [Related]  

  • 11. [Determination of choline and its metabolites in urine and significance of their urinary elimination].
    MARIANI B
    Riv Gastroenterol; 1954; 6(1):1-10. PubMed ID: 13178557
    [No Abstract]   [Full Text] [Related]  

  • 12. Inborn errors of metabolism in acutely sick children.
    Dhareshwar SS; Ambani LM; Suchak RH; Danthi V
    Indian J Med Res; 1982 Nov; 76():716-22. PubMed ID: 7166367
    [No Abstract]   [Full Text] [Related]  

  • 13. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA; Ismail Z; Embong KH; Mohamad SA
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnosis of inborn errors of metabolism.
    Barness LA
    Bol Asoc Med P R; 1969 Nov; 61(11):409-11. PubMed ID: 5262426
    [No Abstract]   [Full Text] [Related]  

  • 15. Screening of high risk infants for metabolic disease in a metropolitan hospital.
    Krieger IE; Nigro M; Sarnaik A; Taqi Q
    J Inherit Metab Dis; 1981; 4(2):81-2. PubMed ID: 6790858
    [No Abstract]   [Full Text] [Related]  

  • 16. [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods].
    Berio A
    Minerva Pediatr; 1972 Jun; 24(32):937-41. PubMed ID: 5050421
    [No Abstract]   [Full Text] [Related]  

  • 17. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
    Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM
    Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Problems in the detection of hereditary diseases studied in the light of frequent examples].
    Vis HL
    Brux Med; 1972 Feb; 52(2):95-100. PubMed ID: 4551157
    [No Abstract]   [Full Text] [Related]  

  • 19. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report].
    Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G
    Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466
    [No Abstract]   [Full Text] [Related]  

  • 20. The screening of hereditary metabolic defects among newborn infants.
    Hsia DY
    Can Med Assoc J; 1966 Aug; 95(6):247-51. PubMed ID: 4380501
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.