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Journal Abstract Search

114 related items for PubMed ID: 3455896

  • 1. Urinary oligosaccharide screening detects type VI glycogen storage disease.
    Sewell AC.
    Clin Chem; 1986 Feb; 32(2):392. PubMed ID: 3455896
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  • 2. An improved thin-layer chromatographic method for urinary oligosaccharide screening.
    Sewell AC.
    Clin Chim Acta; 1979 Mar 15; 92(3):411-4. PubMed ID: 285767
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  • 8. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Mar 15; 42(12):61-71. PubMed ID: 7011274
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  • 10. [Determination of blood level of muscle enzymes in glycogenoses with liver involvement: a diagnostic criterion].
    Labrune P, Chalas J, Pignon JP, Hennion C, Odièvre M.
    Ann Pediatr (Paris); 1989 May 15; 36(5):299-301. PubMed ID: 2742313
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  • 12. Biochemical characteristics and increased tetraglucoside excretion in patients with phosphorylase kinase deficiency.
    Morava E, Wortmann SB, van Essen HZ, Liebrand van Sambeek R, Wevers R, van Diggelen OP.
    J Inherit Metab Dis; 2005 May 15; 28(5):703-6. PubMed ID: 16151901
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  • 13. [Hereditary storage diseases of the liver (author's transl)].
    Schaub J.
    Leber Magen Darm; 1979 Sep 15; 9(5):227-34. PubMed ID: 392211
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  • 16. Urinary oligosaccharides in lysosomal and other metabolic disorders.
    Federico A, Guazzi G.
    Ital J Neurol Sci; 1982 Mar 15; 3(1):7-13. PubMed ID: 7045032
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