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Journal Abstract Search

131 related items for PubMed ID: 7164893

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  • 2. Occurrence of hyperammonemia in the course of 17 cases of methylmalonic acidemia.
    Cathelineau L, Briand P, Ogier H, Charpentier C, Coude FX, Saudubray JM.
    J Pediatr; 1981 Aug; 99(2):279-80. PubMed ID: 7252694
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  • 6. Long term outcome of organic acidurias: survey of 105 French cases (1967-1983).
    Rousson R, Guibaud P.
    J Inherit Metab Dis; 1984 Aug; 7 Suppl 1():10-2. PubMed ID: 6434836
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  • 7. Alanine decreases the protein requirements of infants with inborn errors of amino acid metabolism.
    Wolff JA, Kelts DG, Algert S, Prodanos C, Nyhan WL.
    J Neurogenet; 1985 Feb; 2(1):41-9. PubMed ID: 4020529
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  • 9. Inborn errors of propionate metabolism: methylmalonic and propionic acidaemias.
    Thompson GN.
    J Paediatr Child Health; 1992 Apr; 28(2):134-5. PubMed ID: 1562361
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  • 10. Use of proton nuclear magnetic resonance spectroscopy in detection and study of organic acidurias.
    Iles RA, Hind AJ, Chalmers RA.
    Clin Chem; 1985 Nov; 31(11):1795-801. PubMed ID: 2996806
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  • 12. Pharmacologic amino acid acylation in the acute hyperammonemia of propionic acidemia.
    Petrowski S, Nyhan WL, Reznik V, Sweetman L, Kulovich S, Wolff J, Jones G.
    J Neurogenet; 1987 Apr; 4(2-3):87-96. PubMed ID: 3598771
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  • 14. Carglumic acid: an additional therapy in the treatment of organic acidurias with hyperammonemia?
    Levrat V, Forest I, Fouilhoux A, Acquaviva C, Vianey-Saban C, Guffon N.
    Orphanet J Rare Dis; 2008 Jan 30; 3():2. PubMed ID: 18234091
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  • 18. Hereditary hyperammonaemic syndromes--a six year experience.
    Haan EA, Danks DM, Hoogenraad NJ, Rogers JG.
    Aust Paediatr J; 1979 Sep 30; 15(3):142-6. PubMed ID: 518407
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  • 20. Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases.
    Jan D, Poggi F, Jouvet P, Rabier D, Laurent J, Beringer A, Hubert P, Saudubray JM, Revillon Y.
    Transplant Proc; 1994 Feb 30; 26(1):188. PubMed ID: 8108934
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