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 *

137 related articles for article (PubMed ID: 6790858)

  • 41. [Metabolic screening of newborn and nursing infants].
    Tidskr Sver Sjukskot; 1968 Oct; 35(19):1051. PubMed ID: 5191093
    [No Abstract]   [Full Text] [Related]  

  • 42. Screening for organic acidurias and amino acidopathies in newborns and children.
    Chalmers RA; Purkiss P; Watts RW; Lawson AM
    J Inherit Metab Dis; 1980; 3(2):27-43. PubMed ID: 6777599
    [No Abstract]   [Full Text] [Related]  

  • 43. 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]  

  • 44. Mass screening of the newborn for metabolic disease.
    Woolf LI
    Arch Dis Child; 1968 Apr; 43(228):137-40. PubMed ID: 5645685
    [No Abstract]   [Full Text] [Related]  

  • 45. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A
    Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277
    [No Abstract]   [Full Text] [Related]  

  • 46. Detection of non-volatile organic acids by head-space gas chromatography.
    Heitefuss S; Heine A; Seifert HS
    J Chromatogr; 1990 Nov; 532(2):374-8. PubMed ID: 2084133
    [No Abstract]   [Full Text] [Related]  

  • 47. Simultaneous retention index analysis of urinary amino acids and carboxylic acids for graphic recognition of abnormal state.
    Paik MJ; Lee HJ; Kim KR
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Jul; 821(1):94-104. PubMed ID: 15894518
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Pediatric continuing education. Screening for inborn errors of metabolism.
    Morrow G
    Ariz Med; 1974 Jul; 31(7):520-1. PubMed ID: 4845607
    [No Abstract]   [Full Text] [Related]  

  • 50. The Oregon program of screening for inborn errors of metabolism.
    Ashley CG
    Northwest Med; 1971 Apr; 70(4):268-9. PubMed ID: 5550115
    [No Abstract]   [Full Text] [Related]  

  • 51. URINARY EXCRETION OF PYRUVIC ACID AND LACTIC ACID IN PREMATURE AND FULL-TERM NEWBORN INFANTS.
    TOIVANEN P; DAHL M; TOIVANEN A
    Acta Paediatr (Stockh); 1963 Nov; 52():564-8. PubMed ID: 14082584
    [No Abstract]   [Full Text] [Related]  

  • 52. [Inherited metabolic disorders accompanied with epileptic manifestations].
    Sasaki M; Sakuragawa N
    Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):278-82. PubMed ID: 12483881
    [No Abstract]   [Full Text] [Related]  

  • 53. 3-Methylisoxazol-5-one, an artefact from acetoacetic acid formed during urinary organic acid analysis.
    Mills GA; Walker V; Mellor JM
    Clin Chim Acta; 1989 Sep; 184(1):93-7. PubMed ID: 2598469
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Early recognition of inborn metabolic abnormalities. Methods and results of the Austrian program. II. (Conclusion)].
    Schmierer G
    Med Lab (Stuttg); 1973 May; 26(5):115-9. PubMed ID: 4709319
    [No Abstract]   [Full Text] [Related]  

  • 55. Community screening programmes for metabolic disorders.
    Komrower GM
    Dev Med Child Neurol; 1972 Jun; 14(3):397-9. PubMed ID: 5033825
    [No Abstract]   [Full Text] [Related]  

  • 56. Austria newborn screening programme for inborn errors of metabolism.
    Thalhammer O
    Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784
    [No Abstract]   [Full Text] [Related]  

  • 57. Variable presentation of cytochrome c oxidase deficiency.
    Keppler K; Cunniff C
    Am J Dis Child; 1992 Nov; 146(11):1349-52. PubMed ID: 1329490
    [TBL] [Abstract][Full Text] [Related]  

  • 58. New conjugated urinary metabolites in intermediate type maple syrup urine disease.
    Hagenfeldt L; Naglo AS
    Clin Chim Acta; 1987 Oct; 169(1):77-83. PubMed ID: 3677437
    [TBL] [Abstract][Full Text] [Related]  

  • 59. An evaluation of urine lactate for detection of inborn errors of metabolism.
    Dunger DB; Leonard JV
    J Inherit Metab Dis; 1984; 7 Suppl 2():111-2. PubMed ID: 6434857
    [No Abstract]   [Full Text] [Related]  

  • 60. A practical approach to the diagnosis of metabolic disease in the neonate.
    Collins J
    Dev Med Child Neurol; 1990 Jan; 32(1):79-83. PubMed ID: 2404813
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.