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Journal Abstract Search

139 related items for PubMed ID: 6433137

  • 1. Diagnosing and managing type I and type III glycogen storage diseases.
    Mahoney KG.
    MCN Am J Matern Child Nurs; 1984; 9(5):338-42. PubMed ID: 6433137
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  • 2. 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. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec; 93(12):1423-30. PubMed ID: 8245377
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  • 6. 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; 77(4):531-6. PubMed ID: 3134793
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  • 7. Glycogen storage disease in Israel. A clinical, biochemical and genetic study.
    Levin S, Moses SW, Chayoth R, Jagoda N, Steinitz K.
    Isr J Med Sci; 1967 Jul; 3(3):397-410. PubMed ID: 5317551
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  • 8. Radiography of glycogen storage diseases.
    Miller JH, Stanley P, Gates GF.
    AJR Am J Roentgenol; 1979 Mar; 132(3):379-87. PubMed ID: 106640
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  • 10. The dietary management of hepatic glycogen storage disease.
    Leonard JV, Francis DE, Dunger DB.
    Proc Nutr Soc; 1979 Dec; 38(3):321-4. PubMed ID: 294590
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  • 11. Reversal of debrancher deficiency myopathy by the use of high-protein nutrition.
    Slonim AE, Weisberg C, Benke P, Evans OB, Burr IM.
    Ann Neurol; 1982 Apr; 11(4):420-2. PubMed ID: 7049057
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  • 12. [Hyperlipoproteinemia in glycogenosis and its treatment].
    Chibisov IV, Karmanskiĭ IM.
    Pediatriia; 1982 Feb; (2):6-9. PubMed ID: 6951139
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  • 14. [Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
    Popovich IuG, Chibisov IV, Potapova-Vinogradova IN, Chistova LV.
    Pediatriia; 1988 Feb; (1):35-9. PubMed ID: 3163143
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  • 15. [Continuous nocturnal intragastric feeding in glycogenosis type I and III].
    de Parscau L, Guibaud P, Hermier M, François R.
    Pediatrie; 1986 Feb; 41(3):197-203. PubMed ID: 3095784
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  • 16. [Chinese experts consensus on diagnosis and treatment of glycogen storage disease type Ⅱ in children].
    Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, the Society of Pediatrics, Chinese Medical Association, Society of Medical Genetics, Chinese Medical Association, Subspecialty Group of Rare Diseases, the Society of Pediatrics, Chinese Medical Association, Medical Genetics Branch of Beijing Medical Association, Beijing Rare Disease Diagnosis and Protection Association, China Alliance of Rare Diseases.
    Zhonghua Er Ke Za Zhi; 2021 Jun 02; 59(6):439-445. PubMed ID: 34102815
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  • 19. Liver-spleen scintigraphy in glycogen storage disease (glycogenoses).
    Heyman S.
    Clin Nucl Med; 1985 Dec 02; 10(12):839-43. PubMed ID: 3865755
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