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Journal Abstract Search

126 related items for PubMed ID: 6406667

  • 1.
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  • 2. [Continuous nocturnal intragastric feeding in glycogenosis type I and III].
    de Parscau L, Guibaud P, Hermier M, François R.
    Pediatrie; 1986; 41(3):197-203. PubMed ID: 3095784
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. A new feeding device for treatment of glycogen storage disease.
    Ralstrom CS, O'Riordan M, Krieger I.
    ASDC J Dent Child; 1987 Aug; 54(3):176-8. PubMed ID: 3108340
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  • 5. [Nutritional therapy of glycogen storage disease types I and III].
    Moses SW, Phillip M, Bashan N.
    Harefuah; 1987 Sep; 113(5-6):135-7. PubMed ID: 3121476
    [No Abstract] [Full Text] [Related]

  • 6. Glycogen storage diseases.
    Wolfsdorf JI, Weinstein DA.
    Rev Endocr Metab Disord; 2003 Mar; 4(1):95-102. PubMed ID: 12618563
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  • 7. [Metabolic disorders of the liver.Part 2: glycogen storage diseases, hereditary fructose intolerance, galactosemia and hepatic porphyrias].
    Donner MG, Erhardt A, Häussinger D.
    Dtsch Med Wochenschr; 2010 Dec; 135(50):2540-7. PubMed ID: 21140331
    [No Abstract] [Full Text] [Related]

  • 8. [Treatment of glycogenosis type III with total parenteral nutrition, continuous intragastric infusion and D-thyroxine].
    Böhles H, Dick W, Scharf J.
    Infusionsther Klin Ernahr; 1982 Aug; 9(4):160-1. PubMed ID: 6813261
    [Abstract] [Full Text] [Related]

  • 9. Portacaval shunt for glycogen storage disease and hyperlipidaemia.
    Starzl TE, Putnam CW, Porter KA, Benichou J.
    Ciba Found Symp; 1977 Aug; (55):311-25. PubMed ID: 207496
    [Abstract] [Full Text] [Related]

  • 10. 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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  • 12. Pregnancy associated with amylo-1,6-glucosidase deficiency (Forbe's disease). Case report.
    Confino E, Pauzner D, Lidor A, Yedwab G, David M.
    Br J Obstet Gynaecol; 1984 May; 91(5):494-7. PubMed ID: 6372854
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  • 16. Response to medium chain triglycerides in von Gierke's disease.
    Cuttino JT, Summer GK, Hill HD, Mitchell BJ.
    Pediatrics; 1970 Dec; 46(6):925-9. PubMed ID: 5275632
    [No Abstract] [Full Text] [Related]

  • 17.
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  • 18. Glycogen storage disease type I: effect of continuous nocturnal nasogastric feeding.
    Davidson AG, Wong LT, Kirby L, Tze WJ, Rigg JM, Applegarth DA.
    Monogr Hum Genet; 1978 Dec; 9():29-36. PubMed ID: 104148
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  • 20. Diagnosing and managing type I and type III glycogen storage diseases.
    Mahoney KG.
    MCN Am J Matern Child Nurs; 1984 Dec; 9(5):338-42. PubMed ID: 6433137
    [No Abstract] [Full Text] [Related]

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