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 *

108 related articles for article (PubMed ID: 2824093)

  • 1. Glycogen storage disease type I: laboratory data and diagnosis.
    Wakid NW; Bitar JG; Allam CK
    Clin Chem; 1987 Nov; 33(11):2008-10. PubMed ID: 2824093
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An unusual case of glycogen storage disease.
    Moses SW
    Adv Exp Med Biol; 1973; 41():353-9. PubMed ID: 4364689
    [No Abstract]   [Full Text] [Related]  

  • 3. ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type I.
    Greene HL; Wilson FA; Hefferan P; Terry AB; Moran JR; Slonim AE; Claus TH; Burr IM
    J Clin Invest; 1978 Aug; 62(2):321-8. PubMed ID: 276529
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Continuous nocturnal intragastric feeding for management of type 1 glycogen-storage disease.
    Greene HL; Slonim AE; O'Neill JA; Burr IM
    N Engl J Med; 1976 Feb; 294(8):423-5. PubMed ID: 813144
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and biochemical findings before and after portacaval shunt in a girl with type Ib glycogen storage disease.
    Corbeel L; Hue L; Lederer B; De Barsy T; Van den Berghe G; Devlieger H; Jaeken J; Bracke P; Eeckels R
    Pediatr Res; 1981 Jan; 15(1):58-61. PubMed ID: 6259580
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Continuous glucose monitoring in children with glycogen storage disease type I.
    Kasapkara ÇS; Cinasal Demir G; Hasanoğlu A; Tümer L
    Eur J Clin Nutr; 2014 Jan; 68(1):101-5. PubMed ID: 24149443
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unreliability of platelet glucose-6-phosphatase for the diagnosis of glycogen storage disease type Ia.
    Goldberg JD; Treleaven SC; Koresawa M; Simpson T; Golbus MS
    J Inherit Metab Dis; 1993; 16(5):844-50. PubMed ID: 8295399
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The pathogenesis of hyperuricemia in glycogen storage disease, type I.
    Roe TF; Kogut MD
    Pediatr Res; 1977 May; 11(5):664-9. PubMed ID: 266162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Clinical and biochemical aspects of type I glycogenosis].
    Rossi A la R; Nacagami J; Strufaldi B; Nozaki MJ
    Rev Farm Bioquim Univ Sao Paulo; 1973; 11(2):196-208. PubMed ID: 4373797
    [No Abstract]   [Full Text] [Related]  

  • 10. Hyperuricemia in glycogen storage disease type I. Contributions by hypoglycemia and hyperglucagonemia to increased urate production.
    Cohen JL; Vinik A; Faller J; Fox IH
    J Clin Invest; 1985 Jan; 75(1):251-7. PubMed ID: 2856925
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variability of renal length in type I glycogen storage disease.
    Chen YT; Feinstein KA; Coleman RA; Effmann EL
    J Inherit Metab Dis; 1990; 13(3):259-62. PubMed ID: 2122080
    [No Abstract]   [Full Text] [Related]  

  • 12. Glycogen storage disease type I. Results of treatment with frequent daytime feeding, combined with nocturnal intragastric feeding and with administration of an alpha-glucosidase inhibitor.
    Gröbe H; Ullrich K
    Eur J Pediatr; 1983 Apr; 140(2):102-4. PubMed ID: 6411473
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Heterogeneous phenotypes in Chinese glycogen storage disease type Ia patients with homozygous G727T mutation].
    Qiu ZQ; Wei M; Liu G; Liu GY
    Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):252-5. PubMed ID: 14754525
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Glycogen storage disease type Ia: linkage of glucose, glycogen, lactic acid, triglyceride, and uric acid metabolism.
    Sever S; Weinstein DA; Wolfsdorf JI; Gedik R; Schaefer EJ
    J Clin Lipidol; 2012; 6(6):596-600. PubMed ID: 23312056
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Glucose-6-phosphatase activity in liver and blood platelets of two patients with glycogen storage disease type I.
    Oka Y; Mitsuyama T; Nagai B; Arashima S; Ohkubo I; Matsuda I
    Clin Chim Acta; 1978 Aug; 87(3):319-26. PubMed ID: 209906
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [No Abstract]   [Full Text] [Related]  

  • 17. An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type Ia.
    Fang LJ; Abuduxikuer K; Yan XM; Zhu H; Huang KY
    J Pediatr Endocrinol Metab; 2020 May; 33(6):803-808. PubMed ID: 32436859
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation in the glucose-6-phosphatase gene in Korean twins with glycogen storage disease type Ia.
    Goto M; Taki T; Sugie H; Miki Y; Kato H; Hayashi Y
    J Inherit Metab Dis; 2000 Dec; 23(8):851-2. PubMed ID: 11196115
    [No Abstract]   [Full Text] [Related]  

  • 19. Biochemical diagnosis of type 1b glycogen storage disease.
    Hawkins RA; Kamath KR; Dorney SF; Adams A
    Aust Paediatr J; 1984 Aug; 20(3):217-20. PubMed ID: 6095801
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of glycogen storage disease.
    Reyes LA; Wong PW; Grossman A
    J Pediatr; 1969 May; 74(5):825-6. PubMed ID: 4305187
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.