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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

127 related items for PubMed ID: 1177852

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  • 3. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct; 17(3):297-315. PubMed ID: 5387412
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  • 5. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants.
    Turner B, Brown DA.
    Med J Aust; 1972 Jan 08; 1(2):62-5. PubMed ID: 5025157
    [No Abstract] [Full Text] [Related]

  • 6. [Familial iminoglycinuria].
    Ohura T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 08; (19 Pt 2):569-71. PubMed ID: 9645136
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  • 8. [Hyperprolinemia and hydroxyprolinemia].
    Berger R, Broyer M.
    Presse Med (1893); 1969 May 28; 77(26):957-8. PubMed ID: 5795142
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  • 10. [Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)].
    Lubs H, Baumann H, Kluge G, Machill G.
    Laryngol Rhinol Otol (Stuttg); 1974 Sep 28; 53(9):648-51. PubMed ID: 4419508
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  • 11. Familial pancreatitis associated with hyperglycinuria.
    Bergström K, Hellström K, Kallner M, Lundh G.
    Scand J Gastroenterol; 1973 Sep 28; 8(3):217-23. PubMed ID: 4724921
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  • 12. Hyperprolinemia: clinical and biochemical family study.
    Woody NC, Snyder CH, Harris JA.
    Pediatrics; 1969 Oct 28; 44(4):554-63. PubMed ID: 5346634
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  • 14. Familial iminoglycinuria. An inborn error of renal tubular transport.
    Rosenberg LE, Durant JL, Elsas LJ.
    N Engl J Med; 1968 Jun 27; 278(26):1407-13. PubMed ID: 5652624
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  • 16. [Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
    Minder FC, Dubach UC, Antener I.
    Z Klin Med; 1965 Dec 31; 158(7):601-32. PubMed ID: 5869106
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  • 20. [Results of a survey of search of amino-acidopathies in the north of France. Apropos of 8,433 children].
    Fontaine G, Farriaux JP, Delecour M.
    Ann Pediatr (Paris); 1970 Dec 31; 17(6):487-9. PubMed ID: 5421331
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