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 *

141 related articles for article (PubMed ID: 8295400)

  • 41. Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Enns GM; Bennett MJ; Hoppel CL; Goodman SI; Weisiger K; Ohnstad C; Golabi M; Packman S
    J Pediatr; 2000 Feb; 136(2):251-4. PubMed ID: 10657835
    [TBL] [Abstract][Full Text] [Related]  

  • 42. The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Pons R; Roig M; Riudor E; Ribes A; Briones P; Ortigosa L; Baldellou A; Gil-Gibernau J; Olesti M; Navarro C; Wanders RJ
    Pediatr Neurol; 1996 Apr; 14(3):236-43. PubMed ID: 8736409
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementation.
    Treem WR; Stanley CA; Goodman SI
    J Inherit Metab Dis; 1989; 12(2):112-9. PubMed ID: 2502671
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Lawlor DP; Kalina RE
    Am J Ophthalmol; 1997 Jun; 123(6):846-8. PubMed ID: 9535636
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?
    Holub M; Bodamer OA; Item C; Mühl A; Pollak A; Stöckler-Ipsiroglu S
    Acta Paediatr; 2005 Jan; 94(1):48-52. PubMed ID: 15858960
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein.
    IJlst L; Wanders RJ; Ushikubo S; Kamijo T; Hashimoto T
    Biochim Biophys Acta; 1994 Dec; 1215(3):347-50. PubMed ID: 7811722
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease.
    Yang SY; He XY; Schulz H
    FEBS J; 2005 Oct; 272(19):4874-83. PubMed ID: 16176262
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine.
    Chalmers RA; Roe CR; Stacey TE; Hoppel CL
    Pediatr Res; 1984 Dec; 18(12):1325-8. PubMed ID: 6441143
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Hypoglycaemia without ketosis. A case report].
    Ferraz C; Reis ME; Lopes MM; Cardoso ML; Barbosa CR
    Rev Neurol; 2005 Sep 16-30; 41(6):349-53. PubMed ID: 16163656
    [TBL] [Abstract][Full Text] [Related]  

  • 50. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.
    Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K
    Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: neonatal manifestation at the first day of life presenting with tachypnoea.
    Thiel C; Baudach S; Schnackenberg U; Vreken P; Wanders RJ
    J Inherit Metab Dis; 1999 Oct; 22(7):839-40. PubMed ID: 10518285
    [No Abstract]   [Full Text] [Related]  

  • 52. Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?
    Eaton S; Chatziandreou I; Krywawych S; Pen S; Clayton PT; Hussain K
    Biochem Soc Trans; 2003 Dec; 31(Pt 6):1137-9. PubMed ID: 14641012
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Creatine kinase and uric acid: early warning for metabolic imbalance resulting from disorders of fatty acid oxidation.
    Marsden D; Nyhan WL; Barshop BA
    Eur J Pediatr; 2001 Oct; 160(10):599-602. PubMed ID: 11686503
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Dicarboxylic aciduria in an infant with spinal muscular atrophy.
    Kelley RI; Sladky JT
    Ann Neurol; 1986 Dec; 20(6):734-6. PubMed ID: 3813501
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation.
    Wanders RJ; IJlst L; van Gennip AH; Jakobs C; de Jager JP; Dorland L; van Sprang FJ; Duran M
    J Inherit Metab Dis; 1990; 13(3):311-4. PubMed ID: 2122092
    [No Abstract]   [Full Text] [Related]  

  • 56. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Duran M; Hofkamp M; Rhead WJ; Saudubray JM; Wadman SK
    Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiency.
    Schrijver-Wieling I; van Rens GH; Wittebol-Post D; Smeitink JA; de Jager JP; de Klerk HB; van Lith GH
    Br J Ophthalmol; 1997 Apr; 81(4):291-4. PubMed ID: 9215057
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
    Miyajima H; Orii KE; Shindo Y; Hashimoto T; Shinka T; Kuhara T; Matsumoto I; Shimizu H; Kaneko E
    Neurology; 1997 Sep; 49(3):833-7. PubMed ID: 9305349
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis.
    Hagenfeldt L; von Döbeln U; Holme E; Alm J; Brandberg G; Enocksson E; Lindeberg L
    J Pediatr; 1990 Mar; 116(3):387-92. PubMed ID: 2308028
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.
    Bennett MJ; Weinberger MJ; Kobori JA; Rinaldo P; Burlina AB
    Pediatr Res; 1996 Jan; 39(1):185-8. PubMed ID: 8825408
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.