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 *

255 related articles for article (PubMed ID: 6424667)

  • 1. A new type of glycogen storage disease caused by deficiency of cardiac phosphorylase kinase.
    Mizuta K; Hashimoto E; Tsutou A; Eishi Y; Takemura T; Narisawa K; Yamamura H
    Biochem Biophys Res Commun; 1984 Mar; 119(2):582-7. PubMed ID: 6424667
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Glycogen storage disease confined to the heart with deficient activity of cardiac phosphorylase kinase: a new type of glycogen storage disease.
    Eishi Y; Takemura T; Sone R; Yamamura H; Narisawa K; Ichinohasama R; Tanaka M; Hatakeyama S
    Hum Pathol; 1985 Feb; 16(2):193-7. PubMed ID: 3918928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.
    Lederer B; Van Hoof F; Van den Berghe G; Hers H
    Biochem J; 1975 Apr; 147(1):23-35. PubMed ID: 168880
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liver glycogenosis caused by a defective phosphorylase system: hemolysate analysis.
    Baussan C; Moatti N; Odievre M; Lemonnier A
    Pediatrics; 1981 Jan; 67(1):107-12. PubMed ID: 6787554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Glycogenosis due to liver and muscle phosphorylase kinase deficiency.
    Bashan N; Iancu TC; Lerner A; Fraser D; Potashnik R; Moses SW
    Pediatr Res; 1981 Apr; 15(4 Pt 1):299-303. PubMed ID: 6938920
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle.
    Hug G; Schubert WK; Chuck G
    Biochem Biophys Res Commun; 1970 Aug; 40(4):982-8. PubMed ID: 4322108
    [No Abstract]   [Full Text] [Related]  

  • 7. Infantile glycogen storage myopathy in a girl with phosphorylase kinase deficiency.
    Ohtani Y; Matsuda I; Iwamasa T; Tamari H; Origuchi Y; Miike T
    Neurology; 1982 Aug; 32(8):833-8. PubMed ID: 6285226
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phosphorylation of McArdle phosphorylase induces activity.
    Cerri CG; Willner JH
    Proc Natl Acad Sci U S A; 1981 May; 78(5):2688-92. PubMed ID: 6265901
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Glycogen-storage disease in rats, a genetically determined deficiency of liver phosphorylase kinase.
    Malthus R; Clark DG; Watts C; Sneyd JG
    Biochem J; 1980 Apr; 188(1):99-106. PubMed ID: 6931596
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency.
    Carrier H; Maire I; Vial C; Rambaud G; Flocard F; Flechaire A
    Acta Neuropathol; 1990; 81(1):84-8. PubMed ID: 2128163
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Muscle glycogenosis.
    Moses SW
    J Inherit Metab Dis; 1990; 13(4):452-65. PubMed ID: 2122112
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fatal infantile cardiac glycogenosis with phosphorylase kinase deficiency and a mutation in the gamma2-subunit of AMP-activated protein kinase.
    Akman HO; Sampayo JN; Ross FA; Scott JW; Wilson G; Benson L; Bruno C; Shanske S; Hardie DG; Dimauro S
    Pediatr Res; 2007 Oct; 62(4):499-504. PubMed ID: 17667862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The behavior of hepatic phosphorylase b kinase, phosphorylase a and b after administration of glucagon to patients with glycogen storage disease type VIa.
    Pieniazek D; Pronicka E; Pawłowska J
    Horm Metab Res; 1986 Aug; 18(8):546-50. PubMed ID: 3093350
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Fatal infantile glycogen storage disease: deficiency of phosphofructokinase and phosphorylase b kinase.
    Danon MJ; Carpenter S; Manaligod JR; Schliselfeld LH
    Neurology; 1981 Oct; 31(10):1303-7. PubMed ID: 6213881
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A tentative mechanism of the ternary complex formation between phosphorylase kinase, glycogen phosphorylase b and glycogen.
    Andreeva IE; Makeeva VF; Kurganov BI; Chebotareva NA; Livanova NB
    FEBS Lett; 1999 Feb; 445(1):173-6. PubMed ID: 10069395
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fatal congenital heart glycogenosis caused by a recurrent activating R531Q mutation in the gamma 2-subunit of AMP-activated protein kinase (PRKAG2), not by phosphorylase kinase deficiency.
    Burwinkel B; Scott JW; Bührer C; van Landeghem FK; Cox GF; Wilson CJ; Grahame Hardie D; Kilimann MW
    Am J Hum Genet; 2005 Jun; 76(6):1034-49. PubMed ID: 15877279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency.
    Schimke RN; Zakheim RM; Corder RC; Hug G
    J Pediatr; 1973 Dec; 83(6):1031-4. PubMed ID: 4518931
    [No Abstract]   [Full Text] [Related]  

  • 19. Muscle glycogenolysis. Regulation of the cyclic interconversion of phosphorylase a and phosphorylase b.
    Meinke MH; Edstrom RD
    J Biol Chem; 1991 Feb; 266(4):2259-66. PubMed ID: 1899238
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hepatic phosphorylase b kinase deficiency with normal enzyme activity in erythrocytes and muscle.
    Lozano MJ; Benlloch T; Garcia LV; Garcia Fuentes M
    J Inherit Metab Dis; 1994; 17(1):116-7. PubMed ID: 8051918
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 13.