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PUBMED FOR HANDHELDS

Journal Abstract Search

209 related items for PubMed ID: 5795142

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  • 2. Hydroxyprolinemia: an apparently harmless familial metabolic disorder.
    Pelkonen R, Kivirikko KI.
    N Engl J Med; 1970 Aug 27; 283(9):451-6. PubMed ID: 4393577
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  • 7. Iminoacidopathy in renal failure.
    Simon NM, Bell NH, Del Greco F.
    Arch Intern Med; 1970 Feb 27; 125(2):299-301. PubMed ID: 5412018
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  • 8. [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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  • 11. Biochemical, morphological and hybrid studies in hyperprolinemic mice.
    Kanwar YS, Krakower CA, Manaligod JR, Justice P, Wong PW.
    Biomedicine; 1975 May 24; 22(3):209-16. PubMed ID: 240452
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  • 12. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".
    Statter M, Ben-Zvi A, Shina A, Schein R, Russell A.
    Helv Paediatr Acta; 1976 Aug 24; 31(2):173-82. PubMed ID: 955941
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  • 13. Iminoglycinuria in a child in Czechoslovakia.
    Blehová B, Păzoutová N, Hyánek J, Jirásek J.
    Humangenetik; 1973 Jul 20; 19(2):207-10. PubMed ID: 4744406
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  • 18. [Familial encephalopathy, imino-glycinuria, hydroxyprolinemia].
    Ghisolfi J, Augier D, Fabre J, Delsol G, Régnier C.
    Arch Fr Pediatr; 1972 Apr 20; 29(4):336-7. PubMed ID: 5053204
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  • 19. Familial hyperprolinemia without mental retardation and hereditary nephropathy.
    Mollica F, Pavone L, Antener I.
    Monogr Hum Genet; 1972 Apr 20; 6():144-5. PubMed ID: 4663888
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