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Journal Abstract Search

226 related items for PubMed ID: 3292244

  • 1. Glycogen storage disease: recommendations for treatment.
    Fernandes J, Leonard JV, Moses SW, Odièvre M, di Rocco M, Schaub J, Smit GP, Ullrich K, Durand P.
    Eur J Pediatr; 1988 Apr; 147(3):226-8. PubMed ID: 3292244
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  • 3. Diagnosing and managing type I and type III glycogen storage diseases.
    Mahoney KG.
    MCN Am J Matern Child Nurs; 1984 Apr; 9(5):338-42. PubMed ID: 6433137
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  • 4. Hepatic glycogen storage disorders: what have we learned in recent years?
    Burda P, Hochuli M.
    Curr Opin Clin Nutr Metab Care; 2015 Jul; 18(4):415-21. PubMed ID: 26001652
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  • 6. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Jul; 42(12):61-71. PubMed ID: 7011274
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  • 10. Diet and growth of children with glycogen storage disease Types I and III.
    Daeschel IE, Janick LS, Kramish MJ, Coleman RA.
    J Am Diet Assoc; 1983 Aug; 83(2):135-41. PubMed ID: 6409953
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  • 11. [Hyperlipoproteinemia in glycogenosis and its treatment].
    Chibisov IV, Karmanskiĭ IM.
    Pediatriia; 1982 Feb; (2):6-9. PubMed ID: 6951139
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  • 12. Liver-spleen scintigraphy in glycogen storage disease (glycogenoses).
    Heyman S.
    Clin Nucl Med; 1985 Dec; 10(12):839-43. PubMed ID: 3865755
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  • 13. [Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
    Popovich IuG, Chibisov IV, Potapova-Vinogradova IN, Chistova LV.
    Pediatriia; 1988 Dec; (1):35-9. PubMed ID: 3163143
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  • 14. 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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  • 17. Hepatic ultrasound findings in the glycogen storage diseases.
    Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C.
    Br J Radiol; 1994 Nov 01; 67(803):1062-6. PubMed ID: 7820397
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  • 18. Proceedings: Morphology of liver glycogenosis.
    de Bruijn WC, Fernandes J, Huber J, Koster JF.
    Arch Dis Child; 1975 Aug 01; 50(8):663-4. PubMed ID: 1060439
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  • 19. Glycogen metabolism and glycogen-storage diseases.
    Huijing F.
    Physiol Rev; 1975 Oct 01; 55(4):609-58. PubMed ID: 1103168
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  • 20. Glycogen storage disease type I and III and pyruvate carboxylase deficiency: results of long-term treatment with uncooked cornstarch.
    Ullrich K, Schmidt H, van Teeffelen-Heithoff A.
    Acta Paediatr Scand; 1988 Jul 01; 77(4):531-6. PubMed ID: 3134793
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