메뉴 건너뛰기




Volumn 19, Issue 4, 1996, Pages 478-488

Metabolic intermediates in lactic acidosis: Compounds, samples and interpretation

Author keywords

[No Author keywords available]

Indexed keywords

2 OXOGLUTARIC ACID; 3 HYDROXYBUTYRIC ACID; ACETOACETIC ACID; AMINO ACID; AMMONIA; CARBOXYLIC ACID; CITRULLINE; GLUTAMIC ACID; LACTIC ACID; OXOGLUTARATE DEHYDROGENASE; PYRUVIC ACID;

EID: 0029744874     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799109     Document Type: Article
Times cited : (43)

References (28)
  • 2
    • 0009970034 scopus 로고
    • Biotin-responsive multiple carboxylase deficiency
    • Fernandes J, Saudubray JM, Van den Berghe G, eds. Berlin: Springer-Verlag
    • Baumgartner R, Suormala T (1995) Biotin-responsive multiple carboxylase deficiency. In Fernandes J, Saudubray JM, Van den Berghe G, eds. Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd edn. Berlin: Springer-Verlag, 239-245.
    • (1995) Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd Edn. , pp. 239-245
    • Baumgartner, R.1    Suormala, T.2
  • 3
    • 0347191666 scopus 로고
    • Clinical and metabolic abnormalities accompanying deficiencies in pyruvate oxidation
    • Hommes FA, ed. New York: Wiley-Liss
    • Blass JP, Cederbaum SD, Gibson GE (1983) Clinical and metabolic abnormalities accompanying deficiencies in pyruvate oxidation. In Hommes FA, ed. Normal and Pathological Development of Energy Metabolism. New York: Wiley-Liss, 210-220.
    • (1983) Normal and Pathological Development of Energy Metabolism , pp. 210-220
    • Blass, J.P.1    Cederbaum, S.D.2    Gibson, G.E.3
  • 4
    • 0026711136 scopus 로고
    • Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis
    • Bonnefont JP, Chretien D, Rustin P, et al (1992) Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis. J Pediatr 121: 255-258.
    • (1992) J Pediatr , vol.121 , pp. 255-258
    • Bonnefont, J.P.1    Chretien, D.2    Rustin, P.3
  • 5
    • 0027056128 scopus 로고
    • Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome
    • Bourgeois M, Goutières F, Chrétien D, Rustin P, Munnich A, Aicardi J (1992) Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome. Brain Dev 14: 404-408.
    • (1992) Brain Dev , vol.14 , pp. 404-408
    • Bourgeois, M.1    Goutières, F.2    Chrétien, D.3    Rustin, P.4    Munnich, A.5    Aicardi, J.6
  • 6
    • 0029159804 scopus 로고
    • Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
    • Bourgeron T, Rustin P, Chretien D, et al (1995) Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nature Genet 11: 144-148.
    • (1995) Nature Genet , vol.11 , pp. 144-148
    • Bourgeron, T.1    Rustin, P.2    Chretien, D.3
  • 7
    • 0016764153 scopus 로고
    • Blood sampling techniques for lactate and pyruvate estimation: A reappraisal
    • Braybrooke J, Lloyd B, Nattrass M, Alberti KGMM (1975) Blood sampling techniques for lactate and pyruvate estimation: a reappraisal. Ann Clin Biochem 12: 252-254.
    • (1975) Ann Clin Biochem , vol.12 , pp. 252-254
    • Braybrooke, J.1    Lloyd, B.2    Nattrass, M.3    Alberti, K.G.M.M.4
  • 9
    • 0027049995 scopus 로고
    • Oral glucose lactate stimulation test in mitochondrial disease
    • Chi CS, Mak SC, Shian WJ, Chen CH (1992) Oral glucose lactate stimulation test in mitochondrial disease. Pediatr Neurol 8: 445-449.
    • (1992) Pediatr Neurol , vol.8 , pp. 445-449
    • Chi, C.S.1    Mak, S.C.2    Shian, W.J.3    Chen, C.H.4
  • 11
    • 0019742932 scopus 로고
    • Secondary citrullinemia with hyperammoniemia in four neonatal cases of pyruvate carboxylase deficiency
    • Coudé FX, Ogier H, Marsac C, Munnich A, Charpentier C, Saudubray JM (1981) Secondary citrullinemia with hyperammoniemia in four neonatal cases of pyruvate carboxylase deficiency. Pediatrics 68: 914.
    • (1981) Pediatrics , vol.68 , pp. 914
    • Coudé, F.X.1    Ogier, H.2    Marsac, C.3    Munnich, A.4    Charpentier, C.5    Saudubray, J.M.6
  • 12
    • 0003002955 scopus 로고
    • Glycogen storage diseases
    • Fernandes J, Saudubray JM, Van den Berghe G, eds. Berlin: Springer-Verlag
    • Fernandes J, Chen Y (1995) Glycogen storage diseases. In Fernandes J, Saudubray JM, Van den Berghe G, eds. Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd edn. Berlin: Springer-Verlag, 71-85.
    • (1995) Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd Edn. , pp. 71-85
    • Fernandes, J.1    Chen, Y.2
  • 13
    • 0013640063 scopus 로고
    • Diagnostic procedures: Function tests and postmortem protocol
    • Fernandes J, Saudubray JM, Van den Berghe G, eds. Berlin: Springer-Verlag
    • Fernandes J, Saudubray JM (1995) Diagnostic procedures: function tests and postmortem protocol. In Fernandes J, Saudubray JM, Van den Berghe G, eds. Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd edn. Berlin: Springer-Verlag, 41-46.
    • (1995) Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd Edn. , pp. 41-46
    • Fernandes, J.1    Saudubray, J.M.2
  • 14
    • 0015963110 scopus 로고
    • Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses
    • Fernandes J, Koster JF, Grose WFA, Sorgedrager N (1974) Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses. Arch Dis Child 49: 186-191.
    • (1974) Arch Dis Child , vol.49 , pp. 186-191
    • Fernandes, J.1    Koster, J.F.2    Grose, W.F.A.3    Sorgedrager, N.4
  • 15
    • 0003145008 scopus 로고
    • The pyruvate dehydrogenase complex and tricarboxylic acid cycle
    • Fernandes J, Saudubray JM, Van den Berghe G, eds. Berlin: Springer-Verlag
    • Kerr DS, Zinn AB (1995) The pyruvate dehydrogenase complex and tricarboxylic acid cycle. In Fernandes J, Saudubray JM, Van den Berghe G, eds. Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd edn. Berlin: Springer-Verlag, 109-119.
    • (1995) Inborn Metabolic Diseases: Diagnosis and Treatment, 2nd Edn. , pp. 109-119
    • Kerr, D.S.1    Zinn, A.B.2
  • 18
    • 0029760722 scopus 로고    scopus 로고
    • Metabolic fuel utilization and pyruvate oxidation during the postnatal period
    • Medina JM, Tabernero A, Tovar JA, Martín-Barrientos J (1996) Metabolic fuel utilization and pyruvate oxidation during the postnatal period. J Inher Metab 19: 432-442.
    • (1996) J Inher Metab , vol.19 , pp. 432-442
    • Medina, J.M.1    Tabernero, A.2    Tovar, J.A.3    Martín-Barrientos, J.4
  • 19
    • 0020022069 scopus 로고
    • Congenital lactic acidosis, ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: Dihydrolipoyl dehydrogenase deficiency
    • Munnich A, Saudubray JM, Taylor J, et al (1982) Congenital lactic acidosis, ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency. Acta Paediatr Scand 71: 167-171.
    • (1982) Acta Paediatr Scand , vol.71 , pp. 167-171
    • Munnich, A.1    Saudubray, J.M.2    Taylor, J.3
  • 20
    • 0026680299 scopus 로고
    • Clinical aspects of mitochondrial disorders
    • Munnich A, Rustin P, Rötig A, et al (1992) Clinical aspects of mitochondrial disorders. J Inher Metab Dis 15: 448-455.
    • (1992) J Inher Metab Dis , vol.15 , pp. 448-455
    • Munnich, A.1    Rustin, P.2    Rötig, A.3
  • 21
    • 84985463619 scopus 로고
    • Deficiency of dihydrolipoyl dehydrogenase. A cause of congenital lactic acidosis in infancy
    • Robinson BH, Taylor J, Sherwood WG (1978) Deficiency of dihydrolipoyl dehydrogenase. A cause of congenital lactic acidosis in infancy. Pediatr Res 11: 1198-1203.
    • (1978) Pediatr Res , vol.11 , pp. 1198-1203
    • Robinson, B.H.1    Taylor, J.2    Sherwood, W.G.3
  • 22
    • 0018939283 scopus 로고
    • The genetic heterogeneity of lactic acidosis: Occurrence of recognizable inborn errors of metabolism in pediatric population with lactacidosis
    • Robinson BH, Taylor J, Sherwood WG (1980) The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactacidosis. Pediatr Res 14: 916-926.
    • (1980) Pediatr Res , vol.14 , pp. 916-926
    • Robinson, B.H.1    Taylor, J.2    Sherwood, W.G.3
  • 23
    • 0023146521 scopus 로고
    • 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe
    • 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe. Am J Hum Genet 40: 50-59.
    • (1987) Am J Hum Genet , vol.40 , pp. 50-59
    • Robinson, B.H.1    Oei, J.2    Saudubray, J.M.3
  • 24
    • 0025133424 scopus 로고
    • Pearson's marrow-pancreas syndrome
    • Rötig A, Cormier V, Blanche S, et al (1990) Pearson's marrow-pancreas syndrome. J Clin Invest 86: 1601-1608.
    • (1990) J Clin Invest , vol.86 , pp. 1601-1608
    • Rötig, A.1    Cormier, V.2    Blanche, S.3
  • 26
    • 0023120629 scopus 로고
    • Glycemic thresholds for activation of glucose counterregulatory system are higher than the thresholds for symptoms
    • Schwartz NS, Clutter E, Shah SD, Cryer PE (1987) Glycemic thresholds for activation of glucose counterregulatory system are higher than the thresholds for symptoms. J Clin Invest 79: 777-781.
    • (1987) J Clin Invest , vol.79 , pp. 777-781
    • Schwartz, N.S.1    Clutter, E.2    Shah, S.D.3    Cryer, P.E.4
  • 27
    • 0018045493 scopus 로고
    • Fructose load test - An in vitro screening test designed to assess pyruvate dehydrogenase activity and interconversion
    • Stansbie D, Sherriff RJ (1978) Fructose load test - an in vitro screening test designed to assess pyruvate dehydrogenase activity and interconversion. J Inher Metab Dis 1: 163-165.
    • (1978) J Inher Metab Dis , vol.1 , pp. 163-165
    • Stansbie, D.1    Sherriff, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.