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Journal Abstract Search

130 related items for PubMed ID: 4276001

  • 1. Urinary metabolic screening of mentally retarded patients from institutions in the northern part of Sweden.
    Holmgren G.
    Hum Hered; 1973; 23(6):548-60. PubMed ID: 4276001
    [No Abstract] [Full Text] [Related]

  • 2. Screening for biochemical abnormalities in the urine of the mentally handicapped in Dublin.
    Moore PT, Martin MC, Coffey VP.
    J Ment Defic Res; 1972 Jun; 16(2):128-38. PubMed ID: 4277644
    [No Abstract] [Full Text] [Related]

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  • 5. [Preliminary results in studies of aminoaciduria in progressive muscular dystrophy].
    Górecka A.
    Neurol Neurochir Pol; 1969 Jun; 3(4):431-8. PubMed ID: 5808903
    [No Abstract] [Full Text] [Related]

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  • 7. Aminoacidopathies among institutionalised mentally retarded in Kuwait.
    Yadav G, Farag TI, al Awadi SA, Sam T, Marafie MJ, Bastaki L, el Khalifa MY, Kasrawi B, Wahba RA.
    Clin Genet; 1992 Oct; 42(4):212. PubMed ID: 1424246
    [No Abstract] [Full Text] [Related]

  • 8. Free amino acid levels in amniotic fluid of fetuses affected with Lowe's syndrome or Phenylketonuria.
    Tada K, Higami S, Fujimoto A, Ogita Y.
    Tohoku J Exp Med; 1974 Jun; 113(2):169-71. PubMed ID: 4439401
    [No Abstract] [Full Text] [Related]

  • 9. Aminoaciduria and hyperaminoaciduria in childhood.
    Brodehl J, Bickel H.
    Clin Nephrol; 1973 Jun; 1(3):149-68. PubMed ID: 4593448
    [No Abstract] [Full Text] [Related]

  • 10. [Excretion of acid mucopolysaccharides in a child with Lowe's syndrome].
    Suschke J, Murken JD.
    Monatsschr Kinderheilkd (1902); 1969 May; 117(5):412-4. PubMed ID: 4256689
    [No Abstract] [Full Text] [Related]

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  • 12. Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
    Martin VA, Carson NA.
    Trans Ophthalmol Soc U K (1962); 1967 May; 87():847-70. PubMed ID: 5255262
    [No Abstract] [Full Text] [Related]

  • 13. Homozygous cystinuria and the oculo-cerebro-renal dystrophy of Lowe in same family.
    Bailey RR, Carrell RW, Shannon FT.
    Arch Dis Child; 1976 Jul; 51(7):558-61. PubMed ID: 962366
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  • 14. Amino acid abnormalities in a mentally retarded population.
    Kelly S, Swift H.
    Am J Epidemiol; 1967 Mar; 85(2):250-8. PubMed ID: 6021375
    [No Abstract] [Full Text] [Related]

  • 15. The aminoaciduria of pregnancy.
    Hytten FE, Cheyne GA.
    J Obstet Gynaecol Br Commonw; 1972 May; 79(5):424-32. PubMed ID: 5034379
    [No Abstract] [Full Text] [Related]

  • 16. Urinary screening tests in the infant and young child.
    Bradley GM.
    Med Clin North Am; 1971 Nov; 55(6):1457-71. PubMed ID: 4256889
    [No Abstract] [Full Text] [Related]

  • 17. [Paper chromatographic studies of amino acid excretion in the urine of brain-injured children].
    Schreier K, Porath U, Heinke V.
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):13-6. PubMed ID: 5407727
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  • 19. Report of three cases of mucopolysacchaidoses and an unusual case of hyperaminoaciduria detected during the screening of mentally retarded children.
    Devi KS, Veeraju P, Rao BS.
    Hum Hered; 1994 Jan; 44(2):90-3. PubMed ID: 8188315
    [Abstract] [Full Text] [Related]

  • 20. Argininosuccinic aciduria in hereditary hair diseases.
    Winther A, Bundgaard L.
    Acta Derm Venereol; 1968 Jan; 48(6):567-70. PubMed ID: 4185293
    [No Abstract] [Full Text] [Related]

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