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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

123 related items for PubMed ID: 8870826

  • 1. Pathological study of Japanese quail embryo with acid alpha-glucosidase deficiency during early development.
    Miyagawa-Tomita S, Morishima M, Nakazawa M, Mizutani M, Kikuchi T.
    Acta Neuropathol; 1996 Sep; 92(3):249-54. PubMed ID: 8870826
    [Abstract] [Full Text] [Related]

  • 2. Adeno-associated virus-mediated transfer of human acid maltase gene results in a transient reduction of glycogen accumulation in muscle of Japanese quail with acid maltase deficiency.
    Lin CY, Ho CH, Hsieh YH, Kikuchi T.
    Gene Ther; 2002 May; 9(9):554-63. PubMed ID: 11973631
    [Abstract] [Full Text] [Related]

  • 3. Japanese quail and human acid maltase deficiency: a comparative study.
    Fujita T, Nonaka I, Sugita H.
    Brain Dev; 1991 Jul; 13(4):247-55. PubMed ID: 1957974
    [Abstract] [Full Text] [Related]

  • 4. Mature 98,000-dalton acid alpha-glucosidase is deficient in Japanese quails with acid maltase deficiency.
    Suhara Y, Ishiura S, Tsukahara T, Sugita H.
    Muscle Nerve; 1989 Aug; 12(8):670-8. PubMed ID: 2506448
    [Abstract] [Full Text] [Related]

  • 5. Acid maltase deficiency in the Japanese quail; early morphological event in skeletal muscle.
    Higuchi I, Nonaka I, Usuki F, Ishiura S, Sugita H.
    Acta Neuropathol; 1987 Aug; 73(1):32-7. PubMed ID: 3111161
    [Abstract] [Full Text] [Related]

  • 6. Reappearance of embryonic neutral alpha-glucosidase isoenzyme in acid maltase-deficient muscle of Japanese quail.
    Usuki F, Ishiura S, Higuchi I, Sugita H.
    Exp Neurol; 1988 May; 100(2):394-402. PubMed ID: 3129300
    [Abstract] [Full Text] [Related]

  • 7. Molecular cloning of acid alpha-glucosidase cDNA of Japanese quail (Coturnix coturnix japonica) and the lack of its mRNA in acid maltase deficient quails.
    Kunita R, Nakabayashi O, Wu JY, Hagiwara Y, Mizutani M, Pennybacker M, Chen YT, Kikuchi T.
    Biochim Biophys Acta; 1997 Dec 31; 1362(2-3):269-78. PubMed ID: 9540858
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Adult glycogenosis type II (Pompe's disease): morphological abnormalities in muscle and skin biopsies compared with acid alpha-glucosidase activity.
    Wierzba-Bobrowicz T, Lewandowska E, Lugowska A, Rola R, Stepień T, Ryglewicz D, Pasennik E.
    Folia Neuropathol; 2007 Dec 31; 45(4):179-86. PubMed ID: 18176891
    [Abstract] [Full Text] [Related]

  • 14. [Clinical and molecular genetic study on two patients of the juvenile form of Pompe disease in China].
    Qiu JJ, Wei M, Zhang WM, Shi HP.
    Zhonghua Er Ke Za Zhi; 2007 Oct 31; 45(10):760-4. PubMed ID: 18211760
    [Abstract] [Full Text] [Related]

  • 15. Infantile acid maltase deficiency. II. Muscle fiber hypertrophy and the ultrastructure of end-stage fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Oct 31; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 16. Biopsy-proven alpha-glucosidase deficiency with normal lymphocyte enzyme activity.
    Whitaker CH, Felice KJ, Natowicz M.
    Muscle Nerve; 2004 Mar 31; 29(3):440-2. PubMed ID: 14981745
    [Abstract] [Full Text] [Related]

  • 17. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
    Matsuishi T, Terasawa K, Yoshida I, Yano E, Yamashita F, Hidaka T, Ishihara O, Yoshino M, Nonaka I, Kurokawa T, Nakamura Y.
    Neuropediatrics; 1982 Nov 31; 13(4):173-6. PubMed ID: 6818487
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Replacing acid alpha-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers.
    Raben N, Fukuda T, Gilbert AL, de Jong D, Thurberg BL, Mattaliano RJ, Meikle P, Hopwood JJ, Nagashima K, Nagaraju K, Plotz PH.
    Mol Ther; 2005 Jan 31; 11(1):48-56. PubMed ID: 15585405
    [Abstract] [Full Text] [Related]

  • 20. Glycogenosis type II (acid maltase deficiency).
    Reuser AJ, Kroos MA, Hermans MM, Bijvoet AG, Verbeet MP, Van Diggelen OP, Kleijer WJ, Van der Ploeg AT.
    Muscle Nerve Suppl; 1995 Jan 31; 3():S61-9. PubMed ID: 7603530
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.