BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 14472393)

  • 1. 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]  

  • 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. 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]  

  • 4. MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
    ROWLAND LP; FAHN S; SCHOTLAND DL
    Arch Neurol; 1963 Oct; 9():325-42. PubMed ID: 14055781
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. McArdle's disease--what limit to the age of onset?
    Hewlett RH; Gardner-Thorpe C
    S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Peripheral nerve and vasculature involvement in myophosphorylase deficiency (McArdle's disease).
    Byard RW; Lach B; Preston DN
    Pathology; 1991 Jan; 23(1):62-5. PubMed ID: 2062570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. McArdle's disease: two clinical expressions in the same pedigree.
    Papadimitriou A; Manta P; Divari R; Karabetsos A; Papadimitriou E; Bresolin N
    J Neurol; 1990 Jul; 237(4):267-70. PubMed ID: 2391551
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [McArdle's disease without typical symptoms].
    Watanabe M; Matsubara E; Amari M; Okamoto K; Hirai S
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [McArdle's disease. Apropos of a case].
    Yuste JR; Beloqui O; De la Peña A; Rodríguez-Rosado R; Monreal JI; Prósper F; Prieto J
    Rev Med Univ Navarra; 1998; 42(1):29-33. PubMed ID: 10420954
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low muscle levels of pyridoxine in McArdle's syndrome.
    Haller RG; Dempsey WB; Feit H; Cook JD; Knochel JP
    Am J Med; 1983 Feb; 74(2):217-20. PubMed ID: 6572033
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro.
    Pari G; Crerar MM; Nalbantoglu J; Shoubridge E; Jani A; Tsujino S; Shanske S; DiMauro S; Howell JM; Karpati G
    Neurology; 1999 Oct; 53(6):1352-4. PubMed ID: 10522901
    [TBL] [Abstract][Full Text] [Related]  

  • 15. McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.
    Koster JF; Slee RG; Jennekens FG; Wintzen AR; van Berkel TJ
    Clin Chim Acta; 1979 Jun; 94(3):229-35. PubMed ID: 111879
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P; Nolte J; Meisel D; Dichgans J; Jerusalem F
    Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():1277-80. PubMed ID: 274025
    [No Abstract]   [Full Text] [Related]  

  • 17. Increased muscular beta-hydroxyacyl CoA dehydrogenase with McArdle's disease.
    Turk WR; Heller SL; Norris BJ; Nemeth PM
    Muscle Nerve; 1990 Jul; 13(7):607-12. PubMed ID: 2388659
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myophosphorylase B deficiency and malignant hyperthermia.
    Isaacs H; Badenhorst ME; Du Sautoy C
    Muscle Nerve; 1989 Mar; 12(3):203-5. PubMed ID: 2498654
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. McArdle's disease: biochemical and molecular genetic studies.
    Servidei S; Shanske S; Zeviani M; Lebo R; Fletterick R; DiMauro S
    Ann Neurol; 1988 Dec; 24(6):774-81. PubMed ID: 3207360
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.