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 *

193 related articles for article (PubMed ID: 13909460)

  • 1. [A metabolic disease of muscles: the absence of phosphorylase (McArdle-Schmid-Pearson disease)].
    SCHULLER E
    Presse Med (1893); 1962 Mar; 70():715-7. PubMed ID: 13909460
    [No Abstract]   [Full Text] [Related]  

  • 2. A metabolic myopathy due to absence of muscle phosphorylase.
    PEARSON CM; RIMER DG; MOMMAERTS WF
    Am J Med; 1961 Apr; 30():502-17. PubMed ID: 13733779
    [No Abstract]   [Full Text] [Related]  

  • 3. McArdle's syndrome: phosphorylase-deficient myopathy.
    MELLICK RS; MAHLER RF; HUGHES BP
    Lancet; 1962 May; 1(7238):1045-8. PubMed ID: 14472393
    [No Abstract]   [Full Text] [Related]  

  • 4. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
    Willner JH; Cerri CG; Wood DS; Ponzetto-Zimmerman C; Reydel PM
    Trans Am Neurol Assoc; 1981; 106():208-9. PubMed ID: 6294950
    [No Abstract]   [Full Text] [Related]  

  • 5. [Hepatic glycogenoses. Correlations between the clinical and biochemical characteristics and the type of enzymatic deficiency: glucose-6-phosphatase, amylo-1-6-glucosidase, phosphorylase].
    GABILAN JC
    Rev Int Hepatol; 1960; 10():699-818. PubMed ID: 13702771
    [No Abstract]   [Full Text] [Related]  

  • 6. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
    Coll Cantí J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ
    Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989
    [No Abstract]   [Full Text] [Related]  

  • 7. Muscle glycogen phosphorylase deficiency.
    Moses SW
    Isr J Med Sci; 1989 Feb; 25(2):61-3. PubMed ID: 2703327
    [No Abstract]   [Full Text] [Related]  

  • 8. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.
    Gautron S; Daegelen D; Mennecier F; Dubocq D; Kahn A; Dreyfus JC
    J Clin Invest; 1987 Jan; 79(1):275-81. PubMed ID: 3466902
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phosphorylase and glycogen levels in skeletal muscle of mice with hereditary myopathy.
    LEONARD SL
    Proc Soc Exp Biol Med; 1957 Dec; 96(3):720-2. PubMed ID: 13505838
    [No Abstract]   [Full Text] [Related]  

  • 10. McArdle disease: phosphorylase activity in regenerating muscle fibers.
    Mitsumoto H
    Neurology; 1979 Feb; 29(2):258-62. PubMed ID: 285339
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
    Daegelen D; Munnich A; Levin MJ; Girault A; Goasguen J; Kahn A; Dreyfus JC
    Ann Hum Genet; 1983 May; 47(2):107-15. PubMed ID: 6576726
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.
    Howell JM; Walker KR; Creed KE; Dunton E; Davies L; Quinlivan R; Karpati G
    Neuromuscul Disord; 2014 Feb; 24(2):167-77. PubMed ID: 24309536
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
    Baqué S; Newgard CB; Gerard RD; Guinovart JJ; Gómez-Foix AM
    Biochem J; 1994 Dec; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Metabolic basis of improved exercise tolerance: muscle phosphorylase deficiency after glucagon administration.
    Kono N; Mineo I; Sumi S; Shimizu T; Kang J; Nonaka K; Tarui S
    Neurology; 1984 Nov; 34(11):1471-6. PubMed ID: 6593602
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypoxanthine and Mcardle disease: a clue to metabolic stress in the working forearm.
    Brooke MH; Patterson VH; Kaiser KK
    Muscle Nerve; 1983; 6(3):204-6. PubMed ID: 6574314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiency.
    Schroers A; Kley RA; Stachon A; Horvath R; Lochmüller H; Zange J; Vorgerd M
    Neurology; 2006 Jan; 66(2):285-6. PubMed ID: 16434679
    [No Abstract]   [Full Text] [Related]  

  • 17. [McArdle disease: report of four brothers with myophosphorylase deficiency].
    López Martín A; Baños Madrid RI; García-Estañ Candela J; García Pérez B; Pérez Bautista FJ; Salmerón P
    An Med Interna; 2001 Mar; 18(3):136-8. PubMed ID: 11594178
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse model.
    Brull A; de Luna N; Blanco-Grau A; Lucia A; Martin MA; Arenas J; Martí R; Andreu AL; Pinós T
    J Physiol; 2015 Jun; 593(12):2693-706. PubMed ID: 25873271
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
    FAHN S; SCHOTLAND DL; ROWLAND LP
    Trans Am Neurol Assoc; 1963; 88():145-7. PubMed ID: 14272202
    [No Abstract]   [Full Text] [Related]  

  • 20. 31-P NMR characterization of the metabolic anomalies associated with the lack of glycogen phosphorylase activity in human forearm muscle.
    Bendahan D; Confort-Gouny S; Kozak-Ribbens G; Cozzone PJ
    Biochem Biophys Res Commun; 1992 May; 185(1):16-21. PubMed ID: 1599452
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.