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Journal Abstract Search

668 related items for PubMed ID: 17027861

  • 1. Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.
    Shin YS.
    Semin Pediatr Neurol; 2006 Jun; 13(2):115-20. PubMed ID: 17027861
    [Abstract] [Full Text] [Related]

  • 2. Glycogen storage diseases.
    Hug G.
    Birth Defects Orig Artic Ser; 1976 Jun; 12(6):145-75. PubMed ID: 788807
    [Abstract] [Full Text] [Related]

  • 3. 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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    Stone WL, Basit H, Adil A.
    ; 2024 01. PubMed ID: 29083788
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  • 6. [Genetic heterogeneity and the diagnosis of hepatic glycogenoses].
    Lemonnier A, Baussan C, Moatti N.
    C R Seances Soc Biol Fil; 1984 01; 178(4):327-47. PubMed ID: 6241011
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  • 8. Glycogen storage in multiple muscles of old GSD-II mice can be rapidly cleared after a single intravenous injection with a modified adenoviral vector expressing hGAA.
    Xu F, Ding E, Migone F, Serra D, Schneider A, Chen YT, Amalfitano A.
    J Gene Med; 2005 Feb; 7(2):171-8. PubMed ID: 15515143
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  • 10. Glycogen storage disease type IX: High variability in clinical phenotype.
    Beauchamp NJ, Dalton A, Ramaswami U, Niinikoski H, Mention K, Kenny P, Kolho KL, Raiman J, Walter J, Treacy E, Tanner S, Sharrard M.
    Mol Genet Metab; 2007 Feb; 92(1-2):88-99. PubMed ID: 17689125
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  • 12. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.
    Iwamasa T, Ninomiya N, Fukuda S, Hamada T, Hirashima M, Osame M.
    Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667
    [Abstract] [Full Text] [Related]

  • 13. [Molecular pathology of hepatic glycogen storage disease].
    Inui K.
    Nihon Rinsho; 1993 Feb; 51(2):514-9. PubMed ID: 8385243
    [Abstract] [Full Text] [Related]

  • 14. Molecular genetics of type 1 glycogen storage disease.
    Janecke AR, Mayatepek E, Utermann G.
    Mol Genet Metab; 2001 Jun; 73(2):117-25. PubMed ID: 11386847
    [Abstract] [Full Text] [Related]

  • 15. The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.
    Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S.
    Mol Genet Metab; 2014 Nov; 113(3):171-6. PubMed ID: 25266922
    [Abstract] [Full Text] [Related]

  • 16. An adult case of glycogen storage disease type IIIa.
    Kim KO, Lee HJ, Choi JW, Eun JR, Choi JH.
    Korean J Hepatol; 2008 Jun; 14(2):219-25. PubMed ID: 18617770
    [Abstract] [Full Text] [Related]

  • 17. Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans.
    Maichele AJ, Burwinkel B, Maire I, Søvik O, Kilimann MW.
    Nat Genet; 1996 Nov; 14(3):337-40. PubMed ID: 8896567
    [Abstract] [Full Text] [Related]

  • 18. Glycogen storage disease type IB.
    Buchino JJ, Brown BI, Volk DM.
    Arch Pathol Lab Med; 1983 Jun; 107(6):283-5. PubMed ID: 6303265
    [Abstract] [Full Text] [Related]

  • 19. Glycogen storage diseases in animals and their potential value as models of human disease.
    Walvoort HC.
    J Inherit Metab Dis; 1983 Jun; 6(1):3-16. PubMed ID: 6408305
    [Abstract] [Full Text] [Related]

  • 20. Gene therapy for glycogen storage diseases.
    Kishnani PS, Sun B, Koeberl DD.
    Hum Mol Genet; 2019 Oct 01; 28(R1):R31-R41. PubMed ID: 31227835
    [Abstract] [Full Text] [Related]

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