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Journal Abstract Search

278 related items for PubMed ID: 6791275

  • 1. [Glycogenosis caused by amylo-1,6-glucosidase deficiency. Myopathy as a lead finding in adults].
    Bröker HJ, Kuhn E, Fiehn W, Assmus H, Schröder JM.
    Schweiz Med Wochenschr; 1981 Jun 06; 111(23):854-8. PubMed ID: 6791275
    [Abstract] [Full Text] [Related]

  • 2. 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 06; 13(4):173-6. PubMed ID: 6818487
    [Abstract] [Full Text] [Related]

  • 3.
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    [No Abstract] [Full Text] [Related]

  • 4. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
    Didt L, Winkler M, Bührdel P, Bormann M, Böhme HJ, Hofmann E.
    Z Med Lab Diagn; 1988 Nov 06; 29(1):7-11. PubMed ID: 3129881
    [No Abstract] [Full Text] [Related]

  • 5. [Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].
    Nakagawa M, Nakazato O, Osame M, Nakashima H, Igata A.
    Rinsho Shinkeigaku; 1982 Jan 06; 22(1):57-65. PubMed ID: 6807597
    [No Abstract] [Full Text] [Related]

  • 6. [Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)].
    Lück R, Platt D, Lange RH, Kunze K.
    Z Kinderheilkd; 1975 Jul 01; 120(1):19-28. PubMed ID: 125955
    [Abstract] [Full Text] [Related]

  • 7. Genetic aspects of muscle glycogenosis.
    Moses SW, Bashan N.
    Prog Clin Biol Res; 1989 Jul 01; 306():149-61. PubMed ID: 2500668
    [No Abstract] [Full Text] [Related]

  • 8. 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 Jul 01; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 9. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A, Massin M, Lombet J, Grattagliano B, Soyeur D, Rigo J, Koulischer L, Van Hoof F.
    Am J Med Genet; 1997 Oct 17; 72(2):135-42. PubMed ID: 9382133
    [Abstract] [Full Text] [Related]

  • 10. A new variant form of hepatic glycogenosis with acid maltase deficiency.
    Ninomiya N, Terashima T, Iwamasa T, Matsuda I.
    Jinrui Idengaku Zasshi; 1984 Jun 17; 29(2):113-9. PubMed ID: 6439921
    [No Abstract] [Full Text] [Related]

  • 11. Metabolic myopathies.
    DiMauro S, Miranda AF, Sakoda S, Schon EA, Servidei S, Shanske S, Zeviani M.
    Am J Med Genet; 1986 Dec 17; 25(4):635-51. PubMed ID: 2878616
    [Abstract] [Full Text] [Related]

  • 12. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls].
    Matsuoka Y, Hirayama M, Senda Y, Matsui T.
    Rinsho Shinkeigaku; 1985 Jan 17; 25(1):39-45. PubMed ID: 3922655
    [No Abstract] [Full Text] [Related]

  • 13. [A case of glycogen storage disease with normal acid maltase accompanied with the abnormal platelet function].
    Katsumi Y, Tokonami F, Matsui M, Aii H, Nonaka I.
    Rinsho Shinkeigaku; 1994 Aug 17; 34(8):827-31. PubMed ID: 7994992
    [Abstract] [Full Text] [Related]

  • 14. [A case of glycogen storage myopathy with acute heart failure].
    Nakamura Y, Takahashi M, Maeda M, Yamada Y, Kono N.
    Rinsho Shinkeigaku; 1990 May 17; 30(5):524-8. PubMed ID: 2205434
    [Abstract] [Full Text] [Related]

  • 15. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan 17; 28(1):83-91. PubMed ID: 3133150
    [No Abstract] [Full Text] [Related]

  • 16. 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 17; 11(1):48-56. PubMed ID: 15585405
    [Abstract] [Full Text] [Related]

  • 17. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-1986. A 29-year-old woman with slowly progressive proximal-muscle weakness.
    N Engl J Med; 1986 Sep 11; 315(11):694-701. PubMed ID: 3092049
    [No Abstract] [Full Text] [Related]

  • 18. Developmental study of alpha-glucosidases in Japanese quails with acid maltase deficiency.
    Usuki F, Ishiura S, Sugita H.
    Muscle Nerve; 1986 Sep 11; 9(6):537-43. PubMed ID: 3090432
    [Abstract] [Full Text] [Related]

  • 19. Late familial pseudo-myopathic muscular glycogenosis with alpha 1,4 glucosidase deficiency. Morphological, histoenzymological and biochemical approach.
    Carrier H, Lebel M, Mathieu M, Pialat J, Devic M.
    Pathol Eur; 1975 Sep 11; 10(1):51-9. PubMed ID: 1058451
    [No Abstract] [Full Text] [Related]

  • 20. [26-year-old female patient with elevated liver enzymes].
    Martin K, Schlotter B, Müller-Höcker J, Loeschke K, Pongratz D, Folwaczny C.
    Z Gastroenterol; 2002 Oct 11; 40(10):885-90. PubMed ID: 12436356
    [Abstract] [Full Text] [Related]

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