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 *

290 related articles for article (PubMed ID: 8576570)

  • 1. Primary and secondary carnitine deficiency syndromes.
    Pons R; De Vivo DC
    J Child Neurol; 1995 Nov; 10 Suppl 2():S8-24. PubMed ID: 8576570
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of carnitine in intracellular metabolism.
    Bremer J
    J Clin Chem Clin Biochem; 1990 May; 28(5):297-301. PubMed ID: 2199593
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Carnitine deficiency disorders in children.
    Stanley CA
    Ann N Y Acad Sci; 2004 Nov; 1033():42-51. PubMed ID: 15591002
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: limited diagnostic use of 1-13C fatty acid breath test using bolus technique.
    Jakobs C; Kneer J; Martin D; Boulloche J; Brivet M; Poll-The BT; Saudubray JM
    Eur J Pediatr; 1997 Aug; 156 Suppl 1():S78-82. PubMed ID: 9266222
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Alterations of mitochondria in metabolic diseases. Carnitine deficiency, carnitine palmitoyltransferase deficiency and beta oxidation].
    Angelini C
    Acta Neurol (Napoli); 1989 Oct; 11(5):330-4. PubMed ID: 2603779
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carnitine: a nutritional, biosynthetic, and functional perspective.
    Steiber A; Kerner J; Hoppel CL
    Mol Aspects Med; 2004; 25(5-6):455-73. PubMed ID: 15363636
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Carnitine deficiency].
    Schmidt-Sommerfeld E; Penn D
    Monatsschr Kinderheilkd; 1986 May; 134(5):224-31. PubMed ID: 3014317
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.
    Clark-Taylor T; Clark-Taylor BE
    Med Hypotheses; 2004; 62(6):970-5. PubMed ID: 15142659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disorders of lipid metabolism in muscle.
    Di Mauro S; Trevisan C; Hays A
    Muscle Nerve; 1980; 3(5):369-88. PubMed ID: 7421873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carnitine palmityl transferase I deficiency.
    Al-Aqeel AI; Rashed MS; Ruiter JP; Al-Husseini HF; Al-Amoudi MS; Wanders RJ
    Saudi Med J; 2001 Nov; 22(11):1025-9. PubMed ID: 11744980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Primary carnitine deficiency.
    Scholte HR; Rodrigues Pereira R; de Jonge PC; Luyt-Houwen IE; Hedwig M; Verduin M; Ross JD
    J Clin Chem Clin Biochem; 1990 May; 28(5):351-7. PubMed ID: 2199596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of L-carnitine in pediatric cardiomyopathy.
    Winter S; Jue K; Prochazka J; Francis P; Hamilton W; Linn L; Helton E
    J Child Neurol; 1995 Nov; 10 Suppl 2():S45-51. PubMed ID: 8576569
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Renal handling of carnitine in secondary carnitine deficiency disorders.
    Stanley CA; Berry GT; Bennett MJ; Willi SM; Treem WR; Hale DE
    Pediatr Res; 1993 Jul; 34(1):89-97. PubMed ID: 8356025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Carnitine deficiency in inborn errors of metabolism].
    Sela BA; Lerman-Sagie T; Berkovitz M
    Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of carnitine-dependent metabolic pathways in heart disease without primary ischemia.
    Bremer J; Hokland B
    Z Kardiol; 1987; 76 Suppl 5():9-13. PubMed ID: 3324530
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels.
    Liebig M; Schymik I; Mueller M; Wendel U; Mayatepek E; Ruiter J; Strauss AW; Wanders RJ; Spiekerkoetter U
    Pediatrics; 2006 Sep; 118(3):1065-9. PubMed ID: 16950999
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspects.
    Rubio-Gozalbo ME; Bakker JA; Waterham HR; Wanders RJ
    Mol Aspects Med; 2004; 25(5-6):521-32. PubMed ID: 15363639
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.
    Angelini C; Vergani L; Martinuzzi A
    Crit Rev Clin Lab Sci; 1992; 29(3-4):217-42. PubMed ID: 1489518
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.