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Journal Abstract Search

142 related items for PubMed ID: 14127092

  • 1. DIFFERENTIAL DIAGNOSIS OF THE TYPE OF GLYCOGEN DISEASE IN TWO ADULT PATIENTS WITH LONG HISTORY OF GLYCOGENOSIS.
    VAN CREVELD, HUIJING F.
    Metabolism; 1964 Feb; 13():191-4. PubMed ID: 14127092
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  • 3. Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
    Tuchman M, Brown BI, Burke BA, Ulstrom RA.
    Metabolism; 1986 Jul; 35(7):627-33. PubMed ID: 3459948
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  • 6. [Surgical treatment of glycogenosis].
    Kozaka S, Nishio I, Mizukami T.
    Bruns Beitr Klin Chir (1971); 1969 Jun; 217(4):337-42. PubMed ID: 5264200
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  • 7. Liver glycogenosis. A biochemical and ultrastructural study.
    De Bruijn WC, Fernandes J, Huber J, Koster JF.
    Pathol Eur; 1975 Jun; 10(1):3-15. PubMed ID: 170575
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  • 8. Some cases of Type III glycogen storage disease.
    Rosenfield EL, Popova IA, Chibisov IV.
    Clin Chim Acta; 1976 Mar 01; 67(2):123-30. PubMed ID: 1061645
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  • 14. NEUROPLEGICS IN THE TREATMENT OF BURNS: EXPERIMENTAL AND CLINICAL RESULTS.
    DOLECEK R, ENDRYAS L, KALINA J, KLABUSAY L, JEZEK M.
    J Trauma; 1965 Jan 01; 5():24-42. PubMed ID: 14255172
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  • 16. Hexose monophosphate, pyruvate and lactate in the peripheral blood in glycogen-storage disease type I.
    OEI TL.
    Clin Chim Acta; 1962 Mar 01; 7():193-8. PubMed ID: 14481161
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  • 18. [Glycogenosis type VI and VIa--biochemical and clinical documentation].
    Pieniazek D, Pronicka E, Cabalska B, Borowska B, Miłoszewska E, Maciejko D, Kulczycka H, Prokopowicz K.
    Pediatr Pol; 1985 Jul 01; 60(7):489-96. PubMed ID: 3938009
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  • 19. A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE.
    TOBIN RB, COLEMAN WA.
    Ann Intern Med; 1965 Feb 01; 62():313-27. PubMed ID: 14259214
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  • 20. Studies in type I glycogenosis of the liver. The genesis and disposition of lactate.
    Sadeghi-Nejad A, Presente E, Binkiewicz A, Senior B.
    J Pediatr; 1974 Jul 01; 85(1):49-54. PubMed ID: 4527989
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