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Journal Abstract Search

283 related items for PubMed ID: 14129086

  • 1. HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE.
    GERRITSEN T, WAISMAN HA.
    Pediatrics; 1964 Mar; 33():413-20. PubMed ID: 14129086
    [No Abstract] [Full Text] [Related]

  • 2. HOMOCYSTINURIA.
    KOMROWER GM, WILSON VK.
    Proc R Soc Med; 1963 Nov; 56(11):996-7. PubMed ID: 14084422
    [No Abstract] [Full Text] [Related]

  • 3. HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
    CARSON NA, CUSWORTH DC, DENT CE, FIELD CM, NEILL DW, WESTALL RG.
    Arch Dis Child; 1963 Oct; 38(201):425-36. PubMed ID: 14065982
    [No Abstract] [Full Text] [Related]

  • 4. PATHOLOGICAL FINDINGS IN HOMOCYSTINURIA.
    GIBSON JB, CARSON NA, NEILL DW.
    J Clin Pathol; 1964 Jul; 17(4):427-37. PubMed ID: 14195630
    [Abstract] [Full Text] [Related]

  • 5. [CITRULLINURIA].
    FREYCON F, FREYCON MT.
    Pediatrie; 1963 Jul; 18():847-9. PubMed ID: 14106631
    [No Abstract] [Full Text] [Related]

  • 6. HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE.
    FINKELSTEIN JD, MUDD SH, IRREVERRE F, LASTER L.
    Science; 1964 Nov 06; 146(3645):785-7. PubMed ID: 14197572
    [Abstract] [Full Text] [Related]

  • 7. AN INBORN ERROR OF METABOLISM ASSOCIATED WITH DEFICIENCY OF ENZYME CYSTATHIONINE SYNTHETASE LEADING TO HOMOCYSTINURIA.
    WRIGHT LD.
    N Y State J Med; 1965 Feb 15; 65():559-61. PubMed ID: 14276302
    [No Abstract] [Full Text] [Related]

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  • 9. HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS.
    BRENTON DP, CUSWORTH DC, GAULL GE.
    J Pediatr; 1965 Jul 15; 67():58-68. PubMed ID: 14301559
    [No Abstract] [Full Text] [Related]

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  • 11. HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.
    CARSON NA, DENT CE, FIELD CM, GAULL GE.
    J Pediatr; 1965 Mar 15; 66():565-83. PubMed ID: 14264314
    [No Abstract] [Full Text] [Related]

  • 12. MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
    COFFEY VP.
    J Ir Med Assoc; 1964 Mar 15; 54():84-7. PubMed ID: 14130648
    [No Abstract] [Full Text] [Related]

  • 13. THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.
    DIGEORGE AM, AUERBACH VH.
    Pediatr Clin North Am; 1963 Aug 15; 10():723-44. PubMed ID: 14145016
    [No Abstract] [Full Text] [Related]

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  • 15. [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 15; 72():182-95. PubMed ID: 14136000
    [No Abstract] [Full Text] [Related]

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  • 18. RENAL TUBULAR DISORDERS.
    MILNE MD, LOUGHRIDGE LW.
    Dis Mon; 1964 Oct 15; 89():SUPPL 1964:1+. PubMed ID: 14214262
    [No Abstract] [Full Text] [Related]

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  • 20. EVALUATION OF THE AMINO ACID EXCRETION PATTERN OF MENTAL RETARDATES AS A SCREENING TECHNIQUE FOR INBORN ERRORS OF METABOLISM.
    STAMBAUGH R, DAVIDSON DT.
    J Pediatr; 1964 Aug 15; 65():301-3. PubMed ID: 14198421
    [No Abstract] [Full Text] [Related]

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