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 *

167 related articles for article (PubMed ID: 3655814)

  • 21. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.
    Layzer RB; Havel RJ; McIlroy MB
    Neurology; 1980 Jun; 30(6):627-33. PubMed ID: 7189839
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mitochondrial myopathies.
    DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A case of carnitine palmitoyltransferase II deficiency in human skeletal muscle.
    Singh R; Shepherd IM; Derrick JP; Ramsay RR; Sherratt HS; Turnbull DM
    FEBS Lett; 1988 Dec; 241(1-2):126-30. PubMed ID: 3197828
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Acute rhabdomyolysis with carnitine-palmityl-transferase deficiency.
    Blanc PL; Carrier H; Thomas L; Chavaillon JM; Robert D
    Intensive Care Med; 1982; 8(6):307. PubMed ID: 7175018
    [No Abstract]   [Full Text] [Related]  

  • 25. Carnitine palmitoyltransferase deficiencies.
    Scholte HR; Hülsmann WC; Luyt-Houwen IE; Stinis JT; Jennekens FG
    Biochem Soc Trans; 1985 Aug; 13(4):643-5. PubMed ID: 4029495
    [No Abstract]   [Full Text] [Related]  

  • 26. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency.
    Müller-Höcker J; Paetzke I; Pongratz D; Hübner G
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 48(2):185-96. PubMed ID: 2859691
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases].
    Normand J; Carrier H; Berthillier G; Bozio A; Jocteur-Monrozier D; André M; Joffre B
    Arch Mal Coeur Vaiss; 1979 May; 72(5):529-35. PubMed ID: 115406
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Lipid storage myopathies--carnitine deficiency, carnitine palmitoyltransferase deficiency, pyruvate decarboxylase deficiency].
    Itagaki Y; Nishitani H
    Nihon Rinsho; 1990 Jul; 48(7):1510-6. PubMed ID: 2402068
    [No Abstract]   [Full Text] [Related]  

  • 29. [Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy].
    Lehtonen A; Paljärvi L; Falck B; Somer H; Kalimo H
    Duodecim; 1983; 99(16):1063-9. PubMed ID: 6641545
    [No Abstract]   [Full Text] [Related]  

  • 30. Noninvasive evaluation of adult onset myopathy from carnitine palmitoyl transferase II deficiency using proton magnetic resonance spectroscopy.
    Videen JS; Haseler LJ; Karpinski NC; Terkeltaub RA
    J Rheumatol; 1999 Aug; 26(8):1757-63. PubMed ID: 10451074
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myoglobinuria in carnitine palmityltransferase deficiency.
    Rowett D
    Int Urol Nephrol; 1982; 14(3):285-91. PubMed ID: 7161012
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Deficiency of carnitine palmitoyltransferase in transformed lymphoblasts from a patient having a deficiency of carnitine palmitoyltransferase in skeletal muscle.
    Hostetler KY; Yazaki PJ
    Biochem Biophys Res Commun; 1980 May; 94(1):270-7. PubMed ID: 6248058
    [No Abstract]   [Full Text] [Related]  

  • 33. [Muscular carnitine-palmityl-transferase deficiency].
    Rumpf KW; Kaiser H; Goebel HH; Wagner HA; Ullmann B; DiMauro S; Scheler F
    Dtsch Med Wochenschr; 1983 Jul; 108(27):1058-61. PubMed ID: 6861647
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A case of lipid storage myopathy with carnitine deficiency. Biochemical and electromyographic correlations.
    Scarlato G; Albizzati MG; Bassi S; Cerri C; Frattola L
    Eur Neurol; 1977; 16(1-6):222-9. PubMed ID: 615713
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Heterogeneity of carnitine-palmitoyltransferase deficiency.
    Di Donato S; Castiglione A; Rimoldi M; Cornelio F; Vendemia F; Cardace G; Bertagnolio B
    J Neurol Sci; 1981 May; 50(2):207-15. PubMed ID: 7229666
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hepatic and muscular presentations of carnitine palmitoyl transferase deficiency: two distinct entities.
    Demaugre F; Bonnefont JP; Mitchell G; Nguyen-Hoang N; Pelet A; Rimoldi M; Di Donato S; Saudubray JM
    Pediatr Res; 1988 Sep; 24(3):308-11. PubMed ID: 3211616
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Acute renal insufficiency caused by rhabdomyolysis due to deficiency of carnitine palmitoyltransferase].
    Tafuri A; Della Volpe M; Iberti M; Veronesi GV
    Minerva Nefrol; 1981; 28(4):497-502. PubMed ID: 7339519
    [No Abstract]   [Full Text] [Related]  

  • 38. Exercise-induced recurrent myoglobinuria: defective activity of inner carnitine palmitoyltransferase in muscle mitochondria of two patients.
    Trevisan CP; Isaya G; Angelini C
    Neurology; 1987 Jul; 37(7):1184-8. PubMed ID: 3601082
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Recurrent exertional myalgia and myoglobinuria due to carnitine palmityltransferase deficiency.
    Argov Z; DiMauro S
    Isr J Med Sci; 1983 Jun; 19(6):552-4. PubMed ID: 6862863
    [No Abstract]   [Full Text] [Related]  

  • 40. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J; Nadler HL
    J Pediatr; 1977 Aug; 91(2):247-50. PubMed ID: 874682
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.