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Journal Abstract Search

162 related items for PubMed ID: 3651517

  • 1. Ketogenesis in hypoglycemic neonates. Carnitine and dicarboxylic acids in neonatal hypoglycemia.
    Sann L, Divry P, Cartier B, Vianey-Laud C, Maire I.
    Biol Neonate; 1987; 52(2):80-5. PubMed ID: 3651517
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  • 2. Glucose and ketone body turnover in carnitine-palmitoyl-transferase deficiency.
    Nosadini R, Angelini C, Trevisan C, Vigili de Kreutzenberg S, Fioretto P, Trevisan R, Avogaro A, De Dona C, Doria A, Cobelli C.
    Metabolism; 1987 Sep; 36(9):821-6. PubMed ID: 3626864
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  • 3. Carnitine supplementation and ketogenesis by small-for-date neonates on medium-and long-chain fatty acid formulae.
    Labadaridis J, Mavridou I, Sarafidou G, Alexiou N, Costalos C, Michelakakis H.
    Biol Neonate; 2000 Sep; 77(1):25-8. PubMed ID: 10658827
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  • 4. Neonatal hypoglycaemia in Nepal 2. Availability of alternative fuels.
    de L Costello AM, Pal DK, Manandhar DS, Rajbhandari S, Land JM, Patel N.
    Arch Dis Child Fetal Neonatal Ed; 2000 Jan; 82(1):F52-8. PubMed ID: 10634843
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  • 7. beta-Hydroxybutyrate oxidation is reduced and hepatic balance of ketone bodies and free fatty acids is unaltered in carnitine-depleted, pivalate-treated rats.
    Bianchi PB, Davis AT.
    J Nutr; 1996 Nov; 126(11):2867-72. PubMed ID: 8914959
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  • 8. Parenteral nutrition in preterm neonates with and without carnitine supplementation.
    Larsson LE, Olegård R, Ljung BM, Niklasson A, Rubensson A, Cederblad G.
    Acta Anaesthesiol Scand; 1990 Aug; 34(6):501-5. PubMed ID: 2122630
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  • 9. Ketonuria does not exclude hyperinsulinemic hypoglycemia.
    Wolfsdorf JI, Sadeghi-Nejad A, Senior B.
    Am J Dis Child; 1984 Feb; 138(2):168-71. PubMed ID: 6364785
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  • 10. The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newborn.
    Gregersen N, Ingerslev J.
    Acta Paediatr Scand; 1979 Sep; 68(5):677-81. PubMed ID: 525335
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  • 13. Hepatic ketogenesis and muscle carnitine deficiency.
    DiDonato S, Cornelio F, Storchi G, Rimoldi M.
    Neurology; 1979 Jun; 29(6):780-5. PubMed ID: 572000
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  • 14. Enhanced lipid utilization in infants receiving oral L-carnitine during long-term parenteral nutrition.
    Helms RA, Whitington PF, Mauer EC, Catarau EM, Christensen ML, Borum PR.
    J Pediatr; 1986 Dec; 109(6):984-8. PubMed ID: 3097293
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  • 15. Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood.
    Divry P, David M, Gregersen N, Kølvraa S, Christensen E, Collet JP, Dellamonica C, Cotte J.
    Acta Paediatr Scand; 1983 Nov; 72(6):943-9. PubMed ID: 6673498
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  • 16. Pivalate affects carnitine status but causes no severe metabolic changes in rat liver.
    Nakajima H, Kodo N, Inoue F, Kizaki Z, Nukina S, Kinugasa A, Sawada T.
    J Nutr; 1996 Jun; 126(6):1683-7. PubMed ID: 8648443
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  • 17. Dietary-dependent carnitine deficiency as a cause of nonketotic hypoglycemia in an infant.
    Slonim AE, Borum PR, Tanaka K, Stanley CA, Kasselberg AG, Greene HL, Burr IM.
    J Pediatr; 1981 Oct; 99(4):551-5. PubMed ID: 7277094
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  • 18. [The effect of mildronate on carnitine-dependent and carnitine-independent ketogenesis in rats].
    Simkhovich BZ, Meĭrena DV, Khagi KhB, Shutenko ZhV, Molodchina TN, Kalvin'sh IIa, Lukevits EIa.
    Farmakol Toksikol; 1991 Oct; 54(4):41-2. PubMed ID: 1786824
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  • 20. The influence of intravenous medium- and long-chain triglycerides and carnitine on the excretion of dicarboxylic acids.
    Böhles H, Akçetin Z, Lehnert W.
    JPEN J Parenter Enteral Nutr; 1987 Oct; 11(1):46-8. PubMed ID: 3102781
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