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Journal Abstract Search

104 related items for PubMed ID: 1212727

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  • 3. [Prolinuria].
    Tada K.
    Saishin Igaku; 1969 Jun; 24(6):1226-34. PubMed ID: 5805578
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  • 6. 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; 48(2):225-31. PubMed ID: 5560617
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  • 8. Electroencephalographic findings in three patients with nonketotic hyperglycinemia.
    Seppäläinen AM, Similä S.
    Epilepsia; 1971 Mar; 12(1):101-7. PubMed ID: 5282878
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  • 9. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA, Ismail Z, Embong KH, Mohamad SA.
    Southeast Asian J Trop Med Public Health; 1995 Mar; 26 Suppl 1():130-3. PubMed ID: 8629091
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  • 10. [Nonketone hyperglycinemia].
    Wendt L, Similä S, Kouvalainen K.
    Pediatriia; 1981 May; (5):36-9. PubMed ID: 7279501
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  • 14. Clinical finding and therapeutic problems in non-ketotic hyperglycinemia.
    Koepp P, de Groot CJ, Grüttner R, Rybak C.
    Helv Paediatr Acta; 1973 Nov; 28(5):459-65. PubMed ID: 4773226
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  • 15. An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
    Daum RS, Scriver CR, Mamer OA, Delvin E, Lamm P, Goldman H.
    Pediatr Res; 1973 Mar; 7(3):149-60. PubMed ID: 4690360
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  • 17. Familial neuromuscular disease with nonketotic hyperglycinemia.
    Bank WJ, Morrow G.
    Trans Am Neurol Assoc; 1971 Mar; 96():21-3. PubMed ID: 5159084
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  • 20. Letter: Nonketotic hyperglycinemia with increased propionic acid excretion and hyperammonemia.
    Farriaux JP, Morel P, Hommes FA.
    N Engl J Med; 1976 Mar 04; 294(10):558. PubMed ID: 1250266
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