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Journal Abstract Search

336 related items for PubMed ID: 18471680

  • 21. [Rhabdomyolysis in carnitine palmitoyltransferase deficiency].
    Stavem K, Bjerke G, Skullerud K, Bøhmer T.
    Tidsskr Nor Laegeforen; 1994 Aug 30; 114(20):2398-9. PubMed ID: 7997994
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  • 22. Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency.
    Bennett MJ, Boriack RL, Narayan S, Rutledge SL, Raff ML.
    Mol Genet Metab; 2004 May 30; 82(1):59-63. PubMed ID: 15110323
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  • 23. Carnitine palmitoyltransferase deficiency in a college athlete: a case report and literature review.
    Faigel HC.
    J Am Coll Health; 1995 Sep 30; 44(2):51-4. PubMed ID: 7593992
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  • 24. Anesthetic management of a parturient with carnitine palmitoyltransferase II deficiency.
    Lilker S, Kasodekar S, Goldszmidt E.
    Can J Anaesth; 2006 May 30; 53(5):482-6. PubMed ID: 16636033
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  • 25. Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutations.
    Vladutiu GD, Quackenbush EJ, Hainline BE, Albers S, Smail DS, Bennett MJ.
    J Pediatr; 2002 Nov 30; 141(5):734-6. PubMed ID: 12410208
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  • 26. [Myoglobinuria due to a deficiency of carnitine palmitoyltransferase II. A clinical case report].
    Venturini E, Pupeschi L.
    Recenti Prog Med; 1994 May 30; 85(5):282-3. PubMed ID: 8023007
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  • 29. Recurrent rhabdomyolysis in a collegiate athlete: a case report.
    Krivickas LS.
    Med Sci Sports Exerc; 2006 Mar 30; 38(3):407-10. PubMed ID: 16540825
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  • 33. Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach.
    Vekemans BC, Bonnefont JP, Aupetit J, Royer G, Droin V, Attié-Bitach T, Saudubray JM, Thuillier L.
    Prenat Diagn; 2003 Nov 30; 23(11):884-7. PubMed ID: 14634971
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  • 34. [Carnitine palmitoyltransferase deficiency].
    Yorifuji S.
    Ryoikibetsu Shokogun Shirizu; 2001 Nov 30; (36):54-6. PubMed ID: 11596449
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  • 35. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency.
    Martín MA, Rubio JC, del Hoyo P, García A, Bustos F, Campos Y, Cabello A, Culebras JM, Arenas J.
    Hum Mutat; 2000 Jun 30; 15(6):579-80. PubMed ID: 10862092
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  • 36. A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene.
    Vladutiu GD, Bennett MJ, Smail D, Wong LJ, Taggart RT, Lindsley HB.
    Mol Genet Metab; 2000 Jun 30; 70(2):134-41. PubMed ID: 10873395
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  • 37. [Non-ketotic hypoglycemia caused by carnitine palmitoyl transferase 1 deficiency].
    Rufini S, Bragetti P, Brunelli B, Campolo G, Lato M.
    Pediatr Med Chir; 1993 Jun 30; 15(1):63-6. PubMed ID: 8488129
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  • 38. Adult-onset carnitine palmitoyl transferase II (CPT II) deficiency presenting with rhabdomyolysis and acute kidney injury.
    Akar HT, Yıldız Y, Mutluay R, Tekin E, Tokatlı A.
    CEN Case Rep; 2024 Apr 30; 13(2):81-85. PubMed ID: 37341884
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  • 39. First Japanese Case of Carnitine Palmitoyltransferase II Deficiency with the Homozygous Point Mutation S113L.
    Shima A, Yasuno T, Yamada K, Yamaguchi M, Kohno R, Yamaguchi S, Kido H, Fukuda H.
    Intern Med; 2016 Apr 30; 55(18):2659-61. PubMed ID: 27629963
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  • 40. [Acute renal insufficiency caused by rhabdomyolysis due to deficiency of carnitine palmitoyltransferase].
    Tafuri A, Della Volpe M, Iberti M, Veronesi GV.
    Minerva Nefrol; 1981 Apr 30; 28(4):497-502. PubMed ID: 7339519
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