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Journal Abstract Search

370 related items for PubMed ID: 166513

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  • 3. 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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  • 5. [Glycogen storage disease by amylo 1,6-glucosidase deficiency (author's transl)].
    Méndez Aparicio FM.
    An Esp Pediatr; 1980 Oct 01; 13(10):901-8. PubMed ID: 6937153
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  • 6. Studies of liver glycogenoses, with particular reference to the metabolism of intravenously administered glycerol.
    Senior B, Loridan L.
    N Engl J Med; 1968 Oct 31; 279(18):958-65. PubMed ID: 4300572
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  • 8. Hexose and protein tolerance tests in children with liver glycogenosis caused by a deficiency of the debranching enzyme system.
    Fernandes J, van de Kamer JH.
    Pediatrics; 1968 May 31; 41(5):935-44. PubMed ID: 5240685
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  • 10. Glucose and glycogen metabolism in erythrocytes from normal and glycogen storage disease type III subjects.
    Moses SW, Chayoth R, Levin S, Lazarovitz E, Rubinstein D.
    J Clin Invest; 1968 Jun 31; 47(6):1343-8. PubMed ID: 5240360
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  • 11. Glycogen storage disease type III. A case report.
    de Waal A, Röhm GF, Hoek BB, Potgieter GM, Oosthuysen WT.
    S Afr Med J; 1984 Jan 07; 65(1):23-5. PubMed ID: 6320474
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  • 15. Studies on a patient with in vivo evidence of type I glycogenosis and normal enzyme activities in vitro.
    Chalmers RA, Ryman BE, Watts RW.
    Acta Paediatr Scand; 1978 Mar 07; 67(2):201-7. PubMed ID: 204152
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  • 19. [Hepatic glycogenosis: the clinical, biochemical and enzymatic aspects in a group of pediatric patients].
    Castro de Kolster C, Rolo M, Arias S, Guerreiro N, Carvajal A, Castro J, Kolster J.
    G E N; 1992 Mar 07; 46(3):191-8. PubMed ID: 1340824
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