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Journal Abstract Search

122 related items for PubMed ID: 5652624

  • 21. [Familial essential hyperprolinemia].
    Hainaut H, Hariga J, Willems C, Heusden A, Chapelle P.
    Presse Med (1893); 1971 Apr 24; 79(21):945-8. PubMed ID: 5580522
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  • 23. The ontogeny of amino acid transport in rat kidney. I. Effect on distribution ratios and intracellular metabolism of proline and glycine.
    Baerlocher KE, Scriver CR, Mohyuddin F.
    Biochim Biophys Acta; 1971 Dec 03; 249(2):353-63. PubMed ID: 5134188
    [No Abstract] [Full Text] [Related]

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  • 25. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F, Pavone L, Antener I.
    Pediatrics; 1971 Aug 03; 48(2):225-31. PubMed ID: 5560617
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  • 28. Iminoglycinuria--a "harmless" inborn error of metabolism?
    Fraser GR, Friedmann AI, Patton VM, Wade DN, Woolf LI.
    Humangenetik; 1968 Aug 03; 6(4):362-7. PubMed ID: 5713621
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  • 31. Renal tubular transport of proline, hydroxyproline, and glycine. II. Hydroxy-l-proline as substrate and as inhibitor in vivo.
    Scriver CR, Goldman H.
    J Clin Invest; 1966 Aug 03; 45(8):1357-63. PubMed ID: 5926078
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  • 33. Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids.
    Greene ML, Lietman PS, Rosenberg LE, Seegmiller JE.
    Am J Med; 1973 Feb 03; 54(2):265-71. PubMed ID: 4685850
    [No Abstract] [Full Text] [Related]

  • 34. Aminoaciduria and hyperaminoaciduria in childhood.
    Brodehl J, Bickel H.
    Clin Nephrol; 1973 Feb 03; 1(3):149-68. PubMed ID: 4593448
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  • 35. Membrane transport in disorders of imino-acid metabolism.
    Scriver CR.
    Am J Dis Child; 1967 Jan 03; 113(1):170-4. PubMed ID: 6015898
    [No Abstract] [Full Text] [Related]

  • 36. Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria.
    Vanslambrouck JM, Bröer A, Thavyogarajah T, Holst J, Bailey CG, Bröer S, Rasko JE.
    Biochem J; 2010 May 27; 428(3):397-407. PubMed ID: 20377526
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  • 37. Impaired intestinal transport of proline in a patient with familial iminoaciduria.
    Goodman SI, McIntyre CA, O'Brien D.
    J Pediatr; 1967 Aug 27; 71(2):246-9. PubMed ID: 6029472
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  • 38. A new type of heterozygote of familial renal iminoglycinuria.
    Law EA, Sardharwalla IB.
    Monogr Hum Genet; 1978 Aug 27; 9():152-4. PubMed ID: 732833
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  • 39. [Oculocerebrorenal syndrome in a girl].
    Frézal J, Hors-Cayla MC, Szpiro-Tapia S.
    Arch Fr Pediatr; 1986 Aug 27; 43(7):537. PubMed ID: 3800569
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