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Journal Abstract Search

144 related items for PubMed ID: 7313494

  • 1.
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  • 2. The identification of 3-keto-2-methylvaleric acid and 3-hydroxy-2-methylvaleric acid in a patient with propionic acidemia.
    Truscott RJ, Pullin CJ, Halpern B, Hammond J, Haan E, Danks DM.
    Biomed Mass Spectrom; 1979 Jul; 6(7):294-300. PubMed ID: 486715
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  • 4. Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency.
    Sweetman L, Weyler W, Nyhan WL, de Céspedes C, Loria AR, Estrada Y.
    Biomed Mass Spectrom; 1978 Mar; 5(3):198-207. PubMed ID: 630060
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  • 5. Increased excretion of lactate, glutarate, 3-hydroxyisovalerate and 3-methylglutaconate during clinical episodes of propionic acidemia.
    Kuhara T, Shinka T, Matsuo M, Matsumoto I.
    Clin Chim Acta; 1982 Aug 04; 123(1-2):101-9. PubMed ID: 7116632
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  • 6. [2-Methyl-3-oxovaleric acid: a characteristic metabolite in propionic acidemia].
    Lehnert W, Junker A.
    Clin Chim Acta; 1980 May 21; 104(1):47-51. PubMed ID: 7389125
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  • 7. Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.
    Przyrembel H, Bremer HJ, Duran M, Bruinvis L, Ketting D, Wadman SK, Baumgartner R, Irle U, Bachmann C.
    Eur J Pediatr; 1979 Jan 18; 130(1):1-14. PubMed ID: 759179
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  • 8. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
    Bartlett K, Ng H, Leonard JV.
    Clin Chim Acta; 1980 Jan 15; 100(2):183-6. PubMed ID: 6766095
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  • 9. Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency.
    Goodman SI, McCabe ER, Fennessey PV, Miles BS, Mace JW, Jellum E.
    Clin Chim Acta; 1978 Aug 01; 87(3):441-9. PubMed ID: 28187
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  • 12. Identification of 3-hydroxy-3-ethylglutaric acid in urine of patients with propionic acidaemia.
    Kuhara T, Inoue Y, Shinka T, Matsumoto I, Matsuo M.
    Biomed Mass Spectrom; 1983 Dec 01; 10(12):629-32. PubMed ID: 6200156
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  • 16. Pyroglutamic aciduria in propionyl CoA carboxylase deficiency.
    Morishita H, Nagaya S, Nakajima T, Kawase A, Ohya A, Sugiyama S, Kamiya K, Watanabe I, Togari H, Suzuki Y.
    J Inherit Metab Dis; 1984 Dec 01; 7(3):139-40. PubMed ID: 6438400
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  • 17. Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia.
    Lehnert W, Schuchmann L, Urbánek R, Niederhoff H, Böhm N.
    Eur J Pediatr; 1978 Jul 03; 128(3):197-205. PubMed ID: 668727
    [Abstract] [Full Text] [Related]

  • 18. An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis.
    Pérez-Cerdá C, Merinero B, Martí M, Cabrera JC, Peña L, García MJ, Gangoiti J, Sanz P, Rodríguez-Pombo P, Hoenicka J, Richard E, Muro S, Ugarte M.
    Eur J Pediatr; 1998 Jan 03; 157(1):50-2. PubMed ID: 9461363
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  • 19. Identification of the insertion/deletion mutation in Spanish beta-propionyl-CoA carboxylase-deficient patients.
    Pérez-Cerdá C, Rodríguez-Pombo P, Ugarte M.
    J Inherit Metab Dis; 1994 Jan 03; 17(6):661-3. PubMed ID: 7707688
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