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PUBMED FOR HANDHELDS

Journal Abstract Search


210 related items for PubMed ID: 1024264

  • 21.
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  • 24. [Amino acid metabolism and childhood pathology].
    Netakhata ZhN, Liapun SN.
    Pediatriia; 1970; 49(12):63-73. PubMed ID: 4950145
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  • 26. Screening tests and chromatography for the detection of inborn errors of metabolism.
    Stuber A.
    Clin Chim Acta; 1972 Feb; 36(2):309-13. PubMed ID: 5008795
    [No Abstract] [Full Text] [Related]

  • 27. [Aminoaciduria and aminoacidemia in spinal muscular atrophy].
    Górecka A.
    Neurol Neurochir Pol; 1969 Feb; 3(5):607-12. PubMed ID: 5360553
    [No Abstract] [Full Text] [Related]

  • 28. Tyrosinemia with plantar and palmar keratosis and keratitis.
    Goldsmith LA, Kang E, Bienfang DC, Jimbow K, Gerald P, Baden HP.
    J Pediatr; 1973 Nov; 83(5):798-805. PubMed ID: 4270265
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  • 29. [URINARY ELIMINATION OF THE METABOLITES OF TRYPTOPHAN IN NEUROLOGICAL DISEASES IN CHILDREN. 1. RESULTS IN HYPSARRHYTHMIA, EPILEPSY AND MENTAL RETARDATION WITHOUT CONVULSIONS].
    FOIS A, LECCHINI L.
    Riv Clin Pediatr; 1963 Oct; 72():182-95. PubMed ID: 14136000
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  • 34. The Vodskov Project VII: the amino acids in plasma and urine determined by ion exchange chromatography in a selected patient material and in a normal material.
    Espersen O, Paaby P.
    Dan Med Bull; 1971 Aug; 18(4):88-99. PubMed ID: 5570689
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  • 37. [On some aspects of renal tubule physiopathology in childhood].
    Bottone E, Macchia PA, Baldini G, Bani E.
    Minerva Pediatr; 1973 Jul 14; 25(25):1073-118. PubMed ID: 4356737
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  • 39. Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients.
    Kekomäki M, Visakorpi JK, Perheentupa J, Saxén L.
    Acta Paediatr Scand; 1967 Nov 14; 56(6):617-30. PubMed ID: 6076999
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  • 40. Aminoaciduria in epilepsy.
    CHOREMIS C, KYRIAKIDES V, KARPOUZAS J.
    J Pediatr; 1959 Nov 14; 55():593-601. PubMed ID: 13810005
    [No Abstract] [Full Text] [Related]


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