These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 2203889)

  • 1. Pathophysiology and dietary treatment of the glycogen storage diseases.
    Moses SW
    J Pediatr Gastroenterol Nutr; 1990 Aug; 11(2):155-74. PubMed ID: 2203889
    [No Abstract]   [Full Text] [Related]  

  • 2. Safety issues associated with dietary management in patients with hepatic glycogen storage disease.
    Steunenberg TAH; Peeks F; Hoogeveen IJ; Mitchell JJ; Mundy H; de Boer F; Lubout CMA; de Souza CF; Weinstein DA; Derks TGJ
    Mol Genet Metab; 2018 Sep; 125(1-2):79-85. PubMed ID: 30037503
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Management of hepatic glycogen storage disease with regular oral glucose drinks.
    Dunger DB; Leonard JV
    Proc Nutr Soc; 1979 Dec; 38(3):112A. PubMed ID: 294589
    [No Abstract]   [Full Text] [Related]  

  • 4. McArdle's disease in the 1980s.
    Layzer RB
    N Engl J Med; 1985 Feb; 312(6):370-1. PubMed ID: 3855500
    [No Abstract]   [Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Studies on glycogen and glycogenosis].
    Hers HG
    Verh K Vlaam Acad Geneeskd Belg; 1966; 28(3):369-79. PubMed ID: 5238557
    [No Abstract]   [Full Text] [Related]  

  • 7. The dietary treatment of hepatic glycogen synthetase deficiency.
    Aynsley-Green A; Williamson DH; Gitzelmann R
    Helv Paediatr Acta; 1977 Jun; 32(1):71-5. PubMed ID: 106027
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dietary treatment of liver glycogenosis.
    Andria G; Parenti G; Strisciuglio P; Tinello C
    Beitr Infusionsther; 1991; 27():161-9. PubMed ID: 1713097
    [No Abstract]   [Full Text] [Related]  

  • 9. Type I glycogen storage disease: a metabolic basis for advances in treatment.
    Greene HL; Slonim AE; Burr IM
    Adv Pediatr; 1979; 26():63-92. PubMed ID: 120680
    [No Abstract]   [Full Text] [Related]  

  • 10. Cornstarch therapy in a patient with type III glycogen storage disease.
    Borowitz SM; Greene HL
    J Pediatr Gastroenterol Nutr; 1987; 6(4):631-4. PubMed ID: 3480949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. High-protein feeding in an infant with Pompe's disease.
    Finegold DN; Bergman I
    Neurology; 1988 May; 38(5):824-5. PubMed ID: 3163106
    [No Abstract]   [Full Text] [Related]  

  • 12. Cardiac involvement in glycogen storage disease III: morphologic and biochemical characterization with endomyocardial biopsy.
    Olson LJ; Reeder GS; Noller KL; Edwards WD; Howell RR; Michels VV
    Am J Cardiol; 1984 Mar; 53(7):980-1. PubMed ID: 6584026
    [No Abstract]   [Full Text] [Related]  

  • 13. Intestinal absorption in type I glycogen storage disease.
    Fine RN; Kogut MD; Donnell GN
    J Pediatr; 1969 Oct; 75(4):632-5. PubMed ID: 5258084
    [No Abstract]   [Full Text] [Related]  

  • 14. Glycogen storage disease of the heart--hemodynamic and angiocardiographic features--report of a case.
    Thisyakorn C; Vatanatumrak B
    J Med Assoc Thai; 1978 Feb; 61(2):123-9. PubMed ID: 273061
    [No Abstract]   [Full Text] [Related]  

  • 15. [Therapeutic trials for the patients with muscle glycogen storage diseases].
    Sugie H
    No To Hattatsu; 2004 Mar; 36(2):136-40. PubMed ID: 15031988
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nutritional management of glycogen storage disease.
    Parker PH; Ballew M; Greene HL
    Annu Rev Nutr; 1993; 13():83-109. PubMed ID: 8369161
    [No Abstract]   [Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Pompe's disease in identical twins.
    Agarwala BN
    Hosp Pract (Off Ed); 1986 Mar; 21(3A):146-8, 153, 156-8. PubMed ID: 3081558
    [No Abstract]   [Full Text] [Related]  

  • 20. [Lysosomal glycogen storage disease without acid maltase deficiency(Danon disease)].
    Ohno K
    Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):491-2. PubMed ID: 11032005
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.