These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 6783978)

  • 1. Pyruvate dehydrogenase deficiency restricted to brain.
    Prick M; Gabreëls F; Renier W; Trijbels F; Jaspar H; Lamers K; Kok J
    Neurology; 1981 Apr; 31(4):398-404. PubMed ID: 6783978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.
    Prick MJ; Gabreëls FJ; Renier WO; Trijbels JM; Willems JL; Janssen AJ; Slooff JL; Geelen JA; de Jager JP
    Neuropediatrics; 1982 May; 13(2):108-11. PubMed ID: 6813759
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy.
    Gabreëls FJ; Prick MJ; Trijbels JM; Renier WO; Jaspar HH; Janssen AJ; Slooff JL
    Acta Neurol Scand; 1984 Sep; 70(3):145-54. PubMed ID: 6439001
    [TBL] [Abstract][Full Text] [Related]  

  • 4. "Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis.
    Brown GK; Haan EA; Kirby DM; Scholem RD; Wraith JE; Rogers JG; Danks DM
    Eur J Pediatr; 1988 Jan; 147(1):10-4. PubMed ID: 3123240
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Demyelination and disturbed metabolism of pyruvate: a case report.
    Sengers RC; Trijbels JM; Bakkeren JA; Ruitenbeek W; Janssen AJ; Stadhouders AM; ter Laak HJ
    Eur J Pediatr; 1983 Apr; 140(2):127-30. PubMed ID: 6411474
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosis.
    De Meirleir L; Lissens W; Denis R; Wayenberg JL; Michotte A; Brucher JM; Vamos E; Gerlo E; Liebaers I
    Pediatr Neurol; 1993; 9(3):216-20. PubMed ID: 8352855
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Determination of pyruvate oxidation rate and citric acid cycle activity in intact human leukocytes and fibroblasts.
    Willems HL; de Kort TF; Trijbels FJ; Monnens LA; Veerkamp JH
    Clin Chem; 1978 Feb; 24(2):200-3. PubMed ID: 627049
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 10(1):62-6. PubMed ID: 813176
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)].
    Wendel U; Przyrembel H; Becker K; Walther B; Berger R; Bremer HJ
    Monatsschr Kinderheilkd (1902); 1978 Mar; 126(3):140-7. PubMed ID: 417240
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical diversity of pyruvate dehydrogenase deficiency.
    Cross JH; Connelly A; Gadian DG; Kendall BE; Brown GK; Brown RM; Leonard JV
    Pediatr Neurol; 1994 Jun; 10(4):276-83. PubMed ID: 8068153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Rett syndrome and CSF lactic acid patterns.
    Matsuishi T; Urabe F; Komori H; Yamashita Y; Naito E; Kuroda Y; Horikawa M; Ohtaki E
    Brain Dev; 1992 Jan; 14(1):68-70. PubMed ID: 1590531
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Investigation of enzyme defects in children with lactic acidosis.
    Merinero B; Pérez-Cerda C; Ugarte M
    J Inherit Metab Dis; 1992; 15(5):696-706. PubMed ID: 1331606
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.
    Kuriyama M; Umezaki H; Fukuda Y; Osame M; Koike K; Tateishi J; Igata A
    Neurology; 1984 Jan; 34(1):72-7. PubMed ID: 6537855
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency.
    Shevell MI; Matthews PM; Scriver CR; Brown RM; Otero LJ; Legris M; Brown GK; Arnold DL
    Pediatr Neurol; 1994 Oct; 11(3):224-9. PubMed ID: 7880337
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebrospinal fluid lactate and lactate/pyruvate ratios in hydrocephalus.
    Raisis JE; Kindt GW; McGillicuddy JE; Miller CA
    J Neurosurg; 1976 Mar; 44(3):337-41. PubMed ID: 2652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Problems in the congenital lactic acidoses.
    Leonard JV
    Ciba Found Symp; 1982; 87():340-56. PubMed ID: 6280937
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ketonic diet in the management of pyruvate dehydrogenase deficiency.
    Falk RE; Cederbaum SD; Blass JP; Gibson GE; Kark RA; Carrel RE
    Pediatrics; 1976 Nov; 58(5):713-21. PubMed ID: 824610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients.
    Prick MJ; Gabreëls FJ; Trijbels JM; Janssen AJ; le Coultre R; van Dam K; Jaspar HH; Ebels EJ; Op de Coul AA
    Clin Neurol Neurosurg; 1983; 85(1):57-70. PubMed ID: 6303665
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Studies on pyruvate carboxylase, pyruvate decarboxylase and lipoamide dehydrogenase in subacute necrotizing encephalomyelopathy.
    Hansen TL; Christensen E; Brandt NJ
    Acta Paediatr Scand; 1982 Mar; 71(2):263-7. PubMed ID: 6897146
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Enzymopathic congenital hyperlactacidemia].
    Leroux JP; Marsac C; Saudubray JM
    Ann Biol Clin (Paris); 1976; 34(2):151-9. PubMed ID: 184725
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.