BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 2199596)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophy.
    Scholte HR; Rodrigues Pereira R; Busch HF; Jennekens FG; Luyt-Houwen IE; Vaandrager-Verduin MH
    Wien Klin Wochenschr; 1989 Jan; 101(1):12-7. PubMed ID: 2913721
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. Secondary carnitine deficiency.
    Duran M; Loof NE; Ketting D; Dorland L
    J Clin Chem Clin Biochem; 1990 May; 28(5):359-63. PubMed ID: 2199597
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet.
    Glasgow AM; Engel AG; Bier DM; Perry LW; Dickie M; Todaro J; Brown BI; Utter MF
    Pediatr Res; 1983 May; 17(5):319-26. PubMed ID: 6682967
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A genetic defect in carnitine transport causing primary carnitine deficiency.
    Stanley CA; Treem WR; Hale DE; Coates PM
    Prog Clin Biol Res; 1990; 321():457-64. PubMed ID: 2326306
    [No Abstract]   [Full Text] [Related]  

  • 14. Effect of L-carnitine on mitochondrial acyl CoA esters in the ischemic dog heart.
    Kobayashi A; Fujisawa S
    J Mol Cell Cardiol; 1994 Apr; 26(4):499-508. PubMed ID: 8072006
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carnitine metabolism and human carnitine deficiency.
    Tanphaichitr V; Leelahagul P
    Nutrition; 1993; 9(3):246-54. PubMed ID: 8353366
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Carnitine deficiency and carnitine therapy].
    Künnert B
    Z Gesamte Inn Med; 1988 Jan; 43(1):1-5. PubMed ID: 3281380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy.
    Campos Y; Huertas R; Bautista J; Gutiérrez E; Aparicio M; Lorenzo G; Segura D; Villanueva M; Cabello A; Alesso L
    Muscle Nerve; 1993 Jul; 16(7):778-81. PubMed ID: 8505934
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Carnitine and carnitine palmitoyltransferase in fatty acid oxidation and ketosis.
    Hoppel CL
    Fed Proc; 1982 Oct; 41(12):2853-7. PubMed ID: 7128831
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.