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Journal Abstract Search

214 related items for PubMed ID: 21140331

  • 1. [Metabolic disorders of the liver.Part 2: glycogen storage diseases, hereditary fructose intolerance, galactosemia and hepatic porphyrias].
    Donner MG, Erhardt A, Häussinger D.
    Dtsch Med Wochenschr; 2010 Dec; 135(50):2540-7. PubMed ID: 21140331
    [No Abstract] [Full Text] [Related]

  • 2. [Hereditary storage diseases of the liver (author's transl)].
    Schaub J.
    Leber Magen Darm; 1979 Sep; 9(5):227-34. PubMed ID: 392211
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  • 3. Inborn errors of carbohydrate metabolism.
    Mayatepek E, Hoffmann B, Meissner T.
    Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):607-18. PubMed ID: 20955963
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  • 9. [Nutritional therapy of glycogen storage disease types I and III].
    Moses SW, Phillip M, Bashan N.
    Harefuah; 1987 Sep; 113(5-6):135-7. PubMed ID: 3121476
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  • 10. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Sep; 42(12):61-71. PubMed ID: 7011274
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  • 11. [Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
    Schaub J, Osang M.
    MMW Munch Med Wochenschr; 1976 May 07; 118(19):609-14. PubMed ID: 180406
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  • 12. Hepatic Disorders.
    Mowat AP.
    Clin Gastroenterol; 1982 Jan 07; 11(1):171-205. PubMed ID: 6277534
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  • 14. Glycogen storage diseases in Thai patients: Phramongkutklao Hospital experience.
    Kamolsilp M.
    J Med Assoc Thai; 2005 Nov 07; 88 Suppl 3():S295-301. PubMed ID: 16858972
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  • 17. Patterns of growth in the hepatic glycogenoses.
    Dunger DB, Leonard JV, Preece MA.
    Arch Dis Child; 1984 Jul 07; 59(7):657-60. PubMed ID: 6589977
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  • 19. Impaired platelet function in glucose-6-phosphatase deficiency.
    Corby DG, Putnam CW, Greene HL.
    J Pediatr; 1974 Jul 07; 85(1):71-6. PubMed ID: 4212074
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