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 *

282 related articles for article (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; 111(23):854-8. PubMed ID: 6791275
    [TBL] [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; 13(4):173-6. PubMed ID: 6818487
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
    Meola G; Scarpini E; Manfredi L; Velicogna M; Pellegrini G; Redi CA; Scarlato G
    Basic Appl Histochem; 1984; 28(3):245-55. PubMed ID: 6440527
    [TBL] [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; 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; 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; 120(1):19-28. PubMed ID: 125955
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic aspects of muscle glycogenosis.
    Moses SW; Bashan N
    Prog Clin Biol Res; 1989; 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; 45(1):37-50. PubMed ID: 6199886
    [TBL] [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; 72(2):135-42. PubMed ID: 9382133
    [TBL] [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; 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; 25(4):635-51. PubMed ID: 2878616
    [TBL] [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; 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; 34(8):827-31. PubMed ID: 7994992
    [TBL] [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; 30(5):524-8. PubMed ID: 2205434
    [TBL] [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; 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; 11(1):48-56. PubMed ID: 15585405
    [TBL] [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; 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; 9(6):537-43. PubMed ID: 3090432
    [TBL] [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; 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; 40(10):885-90. PubMed ID: 12436356
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.