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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

128 related items for PubMed ID: 555851

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  • 25. Erythematous skin lesions and partial deficiency of 3-methylcrotonyl-CoA carboxylase in peripheral lymphocytes in a patient with propionic acidaemia.
    Yoshino M, Aramaki S, Yamashita F, Sato K, Inoue Y, Kuhara T, Matsumoto I.
    J Inherit Metab Dis; 1991; 14(5):839-40. PubMed ID: 1779636
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  • 26. Propionic acidemia presenting as pyloric stenosis.
    Katzman PJ, Arnold GL.
    Clin Pediatr (Phila); 1995 Nov; 34(11):613-5. PubMed ID: 8565394
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  • 29. Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia.
    Coude FX, Ogier H, Grimber G, Parvy P, Pham Dinh D, Charpentier C, Saudubray JM.
    Pediatrics; 1982 Jan; 69(1):115-7. PubMed ID: 7054746
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  • 30. Leukocyte propionyl-CoA carboxylase deficiency in a patient with ketotic hyperglycinaemia.
    Del Valle JA, Merinero B, Garciá MJ, Ugarte M, Omeñaca F, Neustadt G.
    J Inherit Metab Dis; 1980 Jan; 3(3):93. PubMed ID: 6775147
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  • 33. Inherited disorders of 3-methylcrotonyl CoA carboxylation.
    Leonard JV, Seakins JW, Bartlett K, Hyde J, Wilson J, Clayton B.
    Arch Dis Child; 1981 Jan; 56(1):53-9. PubMed ID: 7469453
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  • 35. The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.
    Duran M, Bruinvis L, Ketting D, Kamerling JP, Wadman SK, Schutgens RB.
    Biomed Mass Spectrom; 1982 Jan; 9(1):1-5. PubMed ID: 7059658
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  • 36. Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis.
    Wadlington WB, Kilroy A, Ando T, Sweetman L, Nyhan WL.
    J Pediatr; 1975 May; 86(5):707-12. PubMed ID: 1133651
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  • 37. [Blood propionic acid with hyperammonemic coma].
    Stöckler S, Kastner U, Pokits B, Müller W, Roscher A.
    Klin Padiatr; 1987 May; 199(5):348-50. PubMed ID: 3682709
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  • 40. Propionic acidaemia presenting with pancytopaenia in infancy.
    Sweetman L, Nyhan WL, Cravens J, Zomer Y, Plunket DC.
    J Inherit Metab Dis; 1980 May; 2(3):65-9. PubMed ID: 6796762
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