BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 20532823)

  • 1. Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models.
    Spiekerkoetter U; Wood PA
    J Inherit Metab Dis; 2010 Oct; 33(5):539-46. PubMed ID: 20532823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening.
    Spiekerkoetter U
    J Inherit Metab Dis; 2010 Oct; 33(5):527-32. PubMed ID: 20449660
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tissue-specific strategies of the very-long chain acyl-CoA dehydrogenase-deficient (VLCAD-/-) mouse to compensate a defective fatty acid β-oxidation.
    Tucci S; Herebian D; Sturm M; Seibt A; Spiekerkoetter U
    PLoS One; 2012; 7(9):e45429. PubMed ID: 23024820
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation.
    Houten SM; Wanders RJ
    J Inherit Metab Dis; 2010 Oct; 33(5):469-77. PubMed ID: 20195903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disease mechanisms and protein structures in fatty acid oxidation defects.
    Gregersen N; Olsen RK
    J Inherit Metab Dis; 2010 Oct; 33(5):547-53. PubMed ID: 20151199
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long-chain fatty acid oxidation during early human development.
    Oey NA; den Boer ME; Wijburg FA; Vekemans M; Augé J; Steiner C; Wanders RJ; Waterham HR; Ruiter JP; Attié-Bitach T
    Pediatr Res; 2005 Jun; 57(6):755-9. PubMed ID: 15845636
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pathophysiology of fatty acid oxidation disorders.
    Bennett MJ
    J Inherit Metab Dis; 2010 Oct; 33(5):533-7. PubMed ID: 20824345
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Food withdrawal lowers energy expenditure and induces inactivity in long-chain fatty acid oxidation-deficient mouse models.
    Diekman EF; van Weeghel M; Wanders RJ; Visser G; Houten SM
    FASEB J; 2014 Jul; 28(7):2891-900. PubMed ID: 24648546
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting.
    Lindner M; Hoffmann GF; Matern D
    J Inherit Metab Dis; 2010 Oct; 33(5):521-6. PubMed ID: 20373143
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fatty acid oxidation disorders: outcome and long-term prognosis.
    Wilcken B
    J Inherit Metab Dis; 2010 Oct; 33(5):501-6. PubMed ID: 20049534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial dysfunction in fatty acid oxidation disorders: insights from human and animal studies.
    Wajner M; Amaral AU
    Biosci Rep; 2015 Nov; 36(1):e00281. PubMed ID: 26589966
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Current issues regarding treatment of mitochondrial fatty acid oxidation disorders.
    Spiekerkoetter U; Bastin J; Gillingham M; Morris A; Wijburg F; Wilcken B
    J Inherit Metab Dis; 2010 Oct; 33(5):555-61. PubMed ID: 20830526
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and biochemical monitoring of patients with fatty acid oxidation disorders.
    Lund AM; Skovby F; Vestergaard H; Christensen M; Christensen E
    J Inherit Metab Dis; 2010 Oct; 33(5):495-500. PubMed ID: 20066495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
    Gregersen N; Andresen BS; Corydon MJ; Corydon TJ; Olsen RK; Bolund L; Bross P
    Hum Mutat; 2001 Sep; 18(3):169-89. PubMed ID: 11524729
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis.
    Hisahara S; Matsushita T; Furuyama H; Tajima G; Shigematsu Y; Imai T; Shimohama S
    Tohoku J Exp Med; 2015 Apr; 235(4):305-10. PubMed ID: 25843429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency.
    Yamada K; Taketani T
    J Hum Genet; 2019 Feb; 64(2):73-85. PubMed ID: 30401918
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and cellular modifiers of oxidative stress: what can we learn from fatty acid oxidation defects?
    Olsen RK; Cornelius N; Gregersen N
    Mol Genet Metab; 2013; 110 Suppl():S31-9. PubMed ID: 24206932
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Update on mitochondrial fatty acid oxidation disorders.
    Spiekerkoetter U; Mayatepek E
    J Inherit Metab Dis; 2010 Oct; 33(5):467-8. PubMed ID: 20842433
    [No Abstract]   [Full Text] [Related]  

  • 19. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA
    Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid beta-oxidation.
    Schuler AM; Gower BA; Matern D; Rinaldo P; Vockley J; Wood PA
    Mol Genet Metab; 2005 May; 85(1):7-11. PubMed ID: 15862275
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.