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Journal Abstract Search

250 related items for PubMed ID: 568729

  • 1. Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency.
    Di Donato S, Cornelio F, Balestrini MR, Bertagnolio B, Peluchetti D.
    Neurology; 1978 Nov; 28(11):1110-6. PubMed ID: 568729
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  • 2. Case for diagnosis: glycogen-lipid mitochondrial myopathy.
    Woods R.
    Mil Med; 1981 Dec; 146(12):885, 889. PubMed ID: 6799865
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  • 6. Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency.
    Turnbull DM, Bartlett K, Stevens DL, Alberti KG, Gibson GJ, Johnson MA, McCulloch AJ, Sherratt HS.
    N Engl J Med; 1984 Nov 08; 311(19):1232-6. PubMed ID: 6493275
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  • 7. Lipid storage myopathy with normal carnitine levels.
    Jerusalem F, Spiess H, Baumgartner G.
    J Neurol Sci; 1975 Mar 08; 24(3):273-82. PubMed ID: 235012
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  • 11. 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 Mar 08; 16(1-6):222-9. PubMed ID: 615713
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  • 12. Dominantly inherited megalencephaly, muscle weakness, and myoliposis: a carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome.
    Powell BR, Budden SS, Buist NR.
    J Pediatr; 1993 Jul 08; 123(1):70-5. PubMed ID: 8320628
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  • 13. [Carnitine deficiency myopathy].
    Ziegan J, Kühn HJ, Lössner J, Künnert B, Lehmann J.
    Acta Histochem Suppl; 1984 Jul 08; 30():251-5. PubMed ID: 6425943
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  • 16. [Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].
    Pongratz D, Hübner G, Deufel T, Wieland O, Pongratz E, Liphardt R.
    Klin Wochenschr; 1979 Sep 17; 57(18):927-36. PubMed ID: 502358
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  • 18. Infantile Pompe's disease, lipid storage, and partial carnitine deficiency.
    Verity MA.
    Muscle Nerve; 1991 May 17; 14(5):435-40. PubMed ID: 1870635
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