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Journal Abstract Search

276 related items for PubMed ID: 3142324

  • 1. [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency].
    Merinero Cortés B, del Valle Martínez J, Pérez-Cerdá Silvestre C, García Muñoz MJ, Cortés Coto MT, García Aparicio J, Sáez Pérez E, Ugarte Pérez M.
    An Esp Pediatr; 1988 Jul; 29(1):57-60. PubMed ID: 3142324
    [Abstract] [Full Text] [Related]

  • 2. [A case of congenital lactic acidosis caused by deficiency of pyruvate dehydrogenase].
    Salti R, Galluzzi F, Liguri GF, Marianelli L, Zammarchi E, La Cauza C.
    Minerva Pediatr; 1979 Nov 15; 31(21):1539-46. PubMed ID: 118331
    [No Abstract] [Full Text] [Related]

  • 3. Congenital lactic acidosis associated with pyruvate carboxylase deficiency.
    Sagy M, Barzilay Z, Barash V, Oren M, Vardi P, Cohen BE, Gutman A.
    Isr J Med Sci; 1981 Dec 15; 17(12):1159-63. PubMed ID: 6799424
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  • 5. The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis.
    Robinson BH, Taylor J, Sherwood WG.
    Pediatr Res; 1980 Aug 15; 14(8):956-62. PubMed ID: 6775276
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  • 6. [Differential diagnosis of the symptom of lactic acidosis in childhood].
    Koepp P.
    Monatsschr Kinderheilkd; 1984 May 15; 132(5):264-7. PubMed ID: 6087128
    [Abstract] [Full Text] [Related]

  • 7. Lactic acidosis in paediatrics: clinical and laboratory evaluation.
    Stern HJ.
    Ann Clin Biochem; 1994 Sep 15; 31 ( Pt 5)():410-9. PubMed ID: 7832568
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  • 8. Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase.
    Strömme JH, Borud O, Moe PJ.
    Pediatr Res; 1976 Jan 15; 10(1):62-6. PubMed ID: 813176
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  • 9. Lactic acidosis in childhood.
    Israels S, Haworth JC, Dunn HG, Applegarth DA.
    Adv Pediatr; 1976 Jan 15; 22():267-303. PubMed ID: 178159
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  • 10. Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.
    Haworth JC, Perry TL, Blass JP, Hansen S, Urquhart N.
    Pediatrics; 1976 Oct 15; 58(4):564-72. PubMed ID: 184426
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  • 11. Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
    Tada K, Takada G, Omura K, Itokawa Y.
    Eur J Pediatr; 1978 Jan 17; 127(2):141-7. PubMed ID: 203466
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  • 12. Lactic acidosis due to pyruvate carboxylase deficiency.
    Haworth JC, Robinson BH, Perry TL.
    J Inherit Metab Dis; 1981 Jan 17; 4(2):57-8. PubMed ID: 6790846
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  • 13. Pyruvate carboxylase deficiency: acute exacerbation after ACTH treatment of infantile spasms.
    Rutledge SL, Snead OC, Kelly DR, Kerr DS, Swann JW, Spink DL, Martin DL.
    Pediatr Neurol; 1989 Jan 17; 5(4):249-52. PubMed ID: 2553027
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  • 14. [Enzymopathic congenital hyperlactacidemia].
    Leroux JP, Marsac C, Saudubray JM.
    Ann Biol Clin (Paris); 1976 Jan 17; 34(2):151-9. PubMed ID: 184725
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  • 15. Pyruvate-carboxylase deficiency with urea cycle impairment.
    Greter J, Gustafsson J, Holme E.
    Acta Paediatr Scand; 1985 Nov 17; 74(6):982-6. PubMed ID: 3937431
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  • 16. Hepatic fructose-1,6-diphosphatase deficiency. A cause of lactic acidosis and hypoglycemia in infancy.
    Pagliara AS, Karl IE, Keating JP, Brown BI, Kipnis DM.
    J Clin Invest; 1972 Aug 17; 51(8):2115-23. PubMed ID: 4341015
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  • 17. Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency.
    Wong LT, Davidson AG, Applegarth DA, Dimmick JE, Norman MG, Toone JR, Pirie G, Wong J.
    Pediatr Res; 1986 Mar 17; 20(3):274-9. PubMed ID: 3085060
    [Abstract] [Full Text] [Related]

  • 18. Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formula.
    Fattal-Valevski A, Kesler A, Sela BA, Nitzan-Kaluski D, Rotstein M, Mesterman R, Toledano-Alhadef H, Stolovitch C, Hoffmann C, Globus O, Eshel G.
    Pediatrics; 2005 Feb 17; 115(2):e233-8. PubMed ID: 15687431
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