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Journal Abstract Search

446 related items for PubMed ID: 18667910

  • 1.
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  • 3. [Treatment of glycogen storage diseases].
    Endres WT.
    Padiatr Padol; 1991; 26(1):19-24. PubMed ID: 1905390
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  • 4. Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.
    Wolfsdorf JI, Holm IA, Weinstein DA.
    Endocrinol Metab Clin North Am; 1999 Dec; 28(4):801-23. PubMed ID: 10609121
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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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  • 7. [Continuous nocturnal intragastric feeding in glycogenosis type I and III].
    de Parscau L, Guibaud P, Hermier M, François R.
    Pediatrie; 1986 Aug; 41(3):197-203. PubMed ID: 3095784
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  • 9. Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.
    Shin YS.
    Semin Pediatr Neurol; 2006 Jun; 13(2):115-20. PubMed ID: 17027861
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  • 12. 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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  • 13. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
    Kishnani PS, Goldstein J, Austin SL, Arn P, Bachrach B, Bali DS, Chung WK, El-Gharbawy A, Brown LM, Kahler S, Pendyal S, Ross KM, Tsilianidis L, Weinstein DA, Watson MS, ACMG Work Group on Diagnosis and Management of Glycogen Storage Diseases Type VI and IX.
    Genet Med; 2019 Apr; 21(4):772-789. PubMed ID: 30659246
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  • 14. Efficacy of cornstarch therapy in type III glycogen-storage disease.
    Gremse DA, Bucuvalas JC, Balistreri WF.
    Am J Clin Nutr; 1990 Oct; 52(4):671-4. PubMed ID: 2403059
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  • 16. Liver glycogenosis caused by a defective phosphorylase system: hemolysate analysis.
    Baussan C, Moatti N, Odievre M, Lemonnier A.
    Pediatrics; 1981 Jan; 67(1):107-12. PubMed ID: 6787554
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  • 17. [Glycogen synthase deficiency].
    Fukuda T, Sugie H.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan; (18 Pt 1):60-2. PubMed ID: 9589989
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  • 18. Cornstarch therapy in a patient with type III glycogen storage disease.
    Borowitz SM, Greene HL.
    J Pediatr Gastroenterol Nutr; 1987 Jan; 6(4):631-4. PubMed ID: 3480949
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  • 19. Dietary Management of the Glycogen Storage Diseases: Evolution of Treatment and Ongoing Controversies.
    Ross KM, Ferrecchia IA, Dahlberg KR, Dambska M, Ryan PT, Weinstein DA.
    Adv Nutr; 2020 Mar 01; 11(2):439-446. PubMed ID: 31665208
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  • 20. Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations.
    Bachrach BE, Weinstein DA, Orho-Melander M, Burgess A, Wolfsdorf JI.
    J Pediatr; 2002 Jun 01; 140(6):781-3. PubMed ID: 12072888
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