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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

573 related items for PubMed ID: 12799789

  • 21. Therapeutic options in other metabolic myopathies.
    Vorgerd M.
    Neurotherapeutics; 2008 Oct; 5(4):579-82. PubMed ID: 19019309
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  • 22. [2 causes of muscle ache and reddish-brown urine following exertion].
    Jennekens FG, Scholte HR, Koster JF, Bouvy JJ.
    Ned Tijdschr Geneeskd; 1979 Sep 08; 123(36):1562-8. PubMed ID: 289908
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  • 24. Acute renal failure due to carnitine palmitoyltransferase deficiency.
    Berkman N, Meirow D, Katzir Z, Bar-On H.
    J Intern Med; 1993 Mar 08; 233(3):295-7. PubMed ID: 8450300
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  • 28. Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency.
    Patten BM, Wood JM, Harati Y, Hefferan P, Howell RR.
    Am J Med; 1979 Jul 08; 67(1):167-71. PubMed ID: 463910
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  • 35. Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports.
    Avila-Smirnow D, Boutron A, Beytía-Reyes MLÁ, Contreras-Olea O, Caicedo-Feijoo A, Gejman-Enríquez R, Escobar-Henríquez R, Förster-Mujica J.
    J Med Case Rep; 2018 Aug 28; 12(1):249. PubMed ID: 30149802
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  • 36. Complex phenotypes in metabolic muscle diseases.
    Vladutiu GD.
    Muscle Nerve; 2000 Aug 28; 23(8):1157-9. PubMed ID: 10918250
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  • 37. Myoglobinuria, malignant hyperthermia, neuroleptic malignant syndrome and serotonin syndrome.
    Bertorini TE.
    Neurol Clin; 1997 Aug 28; 15(3):649-71. PubMed ID: 9227957
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  • 40. [Acute rhabdomyolysis: a case report and literature review].
    Mrsić V, Nesek Adam V, Grizelj Stojcić E, Rasić Z, Smiljanić A, Turcić I.
    Acta Med Croatica; 2008 Jul 28; 62(3):317-22. PubMed ID: 18843854
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