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Journal Abstract Search

220 related items for PubMed ID: 23941848

  • 1. [Recommendation for the diagnosis of inherited metabolic etiologies in pediatric cardiomyopathy].
    Subspecialty Group of Cardiology, The Society of Pediatrics, Chinese Medical Association, Editorial Board, Chinese Journal of Pediatrics.
    Zhonghua Er Ke Za Zhi; 2013 May; 51(5):385-8. PubMed ID: 23941848
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary metabolic cardiomyopathies.
    Servidei S, Bertini E, DiMauro S.
    Adv Pediatr; 1994 May; 41():1-32. PubMed ID: 7992680
    [No Abstract] [Full Text] [Related]

  • 3. Cardiac involvement in inherited disorders of metabolism.
    Blieden LC, Moller JH.
    Prog Cardiovasc Dis; 1974 May; 16(6):615-31. PubMed ID: 4207425
    [No Abstract] [Full Text] [Related]

  • 4. Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism.
    Towbin JA, Jefferies JL.
    Circ Res; 2017 Sep 15; 121(7):838-854. PubMed ID: 28912186
    [Abstract] [Full Text] [Related]

  • 5. [Importance of the culture of cells in vitro for the diagnosis and study of metabolic diseases].
    Esposito G.
    Pediatria (Napoli); 1971 Sep 15; 79(2):270-83. PubMed ID: 4255382
    [No Abstract] [Full Text] [Related]

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  • 8. ["Metabolic" myocardiopathies in childhood (author's transl)].
    Kachaner J, Batisse A, Fermont L, Piechaud JF, Ribierre M.
    Ann Pediatr (Paris); 1981 Mar 15; 28(5):345-50. PubMed ID: 6787971
    [No Abstract] [Full Text] [Related]

  • 9. Metabolic myopathies: a guide and update for clinicians.
    Burr ML, Roos JC, Ostör AJ.
    Curr Opin Rheumatol; 2008 Nov 15; 20(6):639-47. PubMed ID: 18946322
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  • 11. A new look at the inborn errors of metabolism.
    Sinclair L.
    Ann Clin Biochem; 1982 Jul 15; 19 (Pt 4)():314-21. PubMed ID: 6812485
    [No Abstract] [Full Text] [Related]

  • 12. Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.
    Voermans NC, van Engelen BG, Kluijtmans LA, Stikkelbroeck NM, Hermus AR.
    Am J Med; 2006 Feb 15; 119(2):176-9. PubMed ID: 16443431
    [No Abstract] [Full Text] [Related]

  • 13. Metabolic myopathies: a clinical approach; part II.
    Darras BT, Friedman NR.
    Pediatr Neurol; 2000 Mar 15; 22(3):171-81. PubMed ID: 10734246
    [Abstract] [Full Text] [Related]

  • 14. Clinical and biochemical footprints of inherited metabolic diseases. IV. Metabolic cardiovascular disease.
    Ferreira CR, Blau N.
    Mol Genet Metab; 2021 Feb 15; 132(2):112-118. PubMed ID: 33388235
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  • 18. Clinical practice and the development of evidence.
    Wilcken B.
    J Inherit Metab Dis; 2012 Jan 15; 35(1):3-4. PubMed ID: 21863278
    [No Abstract] [Full Text] [Related]

  • 19. Enzymatic and biochemical diagnosis of inborn lysosomal diseases with neurological symptoms.
    Hultberg B, Ockerman PA, Sjöblad S.
    Eur Neurol; 1972 Jan 15; 7(1):101-18. PubMed ID: 4259742
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