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Journal Abstract Search

224 related items for PubMed ID: 1905390

  • 1. [Treatment of glycogen storage diseases].
    Endres WT.
    Padiatr Padol; 1991; 26(1):19-24. PubMed ID: 1905390
    [Abstract] [Full Text] [Related]

  • 2. Nutritional therapy for glycogen storage diseases.
    Heller S, Worona L, Consuelo A.
    J Pediatr Gastroenterol Nutr; 2008 Aug; 47 Suppl 1():S15-21. PubMed ID: 18667910
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  • 4. 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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  • 5. 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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  • 6. Glycogen storage diseases.
    Hug G.
    Birth Defects Orig Artic Ser; 1976 Aug; 12(6):145-75. PubMed ID: 788807
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  • 8. [Carbohydrates in the treatment of glycogenoses].
    Hayde M, Widhalm K.
    Infusionstherapie; 1990 Apr; 17(2):69-72. PubMed ID: 2113038
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  • 9. Inborn errors of carbohydrate metabolism.
    Mayatepek E, Hoffmann B, Meissner T.
    Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):607-18. PubMed ID: 20955963
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  • 10. [Type I glycogenosis: extending therapy with uncooked cornstarch].
    Biggemann B, Hilgarth R, Wendel U.
    Monatsschr Kinderheilkd; 1986 Mar; 134(3):142-5. PubMed ID: 3084952
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  • 11. Glycogen storage diseases in Thai patients: Phramongkutklao Hospital experience.
    Kamolsilp M.
    J Med Assoc Thai; 2005 Nov; 88 Suppl 3():S295-301. PubMed ID: 16858972
    [Abstract] [Full Text] [Related]

  • 12. Molecular prenatal diagnosis of glycogen storage disease type Ia.
    Qu Y, Abdenur JE, Eng CM, Desnick RJ.
    Prenat Diagn; 1996 Apr; 16(4):333-6. PubMed ID: 8734807
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  • 13. Gastric drip feeding in patients with glycogen storage disease type I: its effects on growth and plasma lipids and apolipoproteins.
    Fernandes J, Alaupovic P, Wit JM.
    Pediatr Res; 1989 Apr; 25(4):327-31. PubMed ID: 2542871
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  • 14. Review of the glycogen storage diseases.
    Bitar J.
    J Med Liban; 1986 Apr; 36(2):72-5. PubMed ID: 3537297
    [No Abstract] [Full Text] [Related]

  • 15. 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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  • 18. Prenatal diagnosis of glycogen storage disease type 1a by direct mutation detection.
    Wong LJ.
    Prenat Diagn; 1996 Feb; 16(2):105-8. PubMed ID: 8650119
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  • 19. Glycogen storage diseases: a brief review and update on clinical features, genetic abnormalities, pathologic features, and treatment.
    Hicks J, Wartchow E, Mierau G.
    Ultrastruct Pathol; 2011 Oct; 35(5):183-96. PubMed ID: 21910565
    [Abstract] [Full Text] [Related]

  • 20. Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes.
    Kido J, Nakamura K, Matsumoto S, Mitsubuchi H, Ohura T, Shigematsu Y, Yorifuji T, Kasahara M, Horikawa R, Endo F.
    J Hum Genet; 2013 May; 58(5):285-92. PubMed ID: 23486339
    [Abstract] [Full Text] [Related]

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