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4. [Glycogenosis due to a defect of liver phosphorylase-kinase (glycogenosis type IX). A clinical, biochemical, and electron-microscopy study]. Mardesić D; Jadro-Santel D; Crnojević-Ivanusić R; Lipovac K; Juretić D Acta Med Iugosl; 1978; 32(1):75-91. PubMed ID: 274067 [No Abstract] [Full Text] [Related]
5. 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]
6. [Treatment of glycogenosis type III with total parenteral nutrition, continuous intragastric infusion and D-thyroxine]. Böhles H; Dick W; Scharf J Infusionsther Klin Ernahr; 1982 Aug; 9(4):160-1. PubMed ID: 6813261 [TBL] [Abstract][Full Text] [Related]
7. [Different phenotypes of type IXb glycogenosis (phosphorylase-b-kinase deficiency) in adult- and early childhood]. Müller P; Bührdel P; Freidt B; Böhme HJ Med Klin (Munich); 1996 Oct; 91(10):667-9. PubMed ID: 9019646 [No Abstract] [Full Text] [Related]
9. 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]
10. Deficient activity of dephosphophosphorylase kinase and accumulation of glycogen in the liver. Hug G; Schubert WK; Chuck G J Clin Invest; 1969 Apr; 48(4):704-15. PubMed ID: 5774108 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases. Burwinkel B; Hu B; Schroers A; Clemens PR; Moses SW; Shin YS; Pongratz D; Vorgerd M; Kilimann MW Eur J Hum Genet; 2003 Jul; 11(7):516-26. PubMed ID: 12825073 [TBL] [Abstract][Full Text] [Related]
13. Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans. Maichele AJ; Burwinkel B; Maire I; Søvik O; Kilimann MW Nat Genet; 1996 Nov; 14(3):337-40. PubMed ID: 8896567 [TBL] [Abstract][Full Text] [Related]
15. [Glycogenosis type VI and VIa--biochemical and clinical documentation]. Pieniazek D; Pronicka E; Cabalska B; Borowska B; Miłoszewska E; Maciejko D; Kulczycka H; Prokopowicz K Pediatr Pol; 1985 Jul; 60(7):489-96. PubMed ID: 3938009 [No Abstract] [Full Text] [Related]
16. The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patients. Willems PJ; Gerver WJ; Berger R; Fernandes J Eur J Pediatr; 1990 Jan; 149(4):268-71. PubMed ID: 2303074 [TBL] [Abstract][Full Text] [Related]
17. Liver glycogenosis. A biochemical and ultrastructural study. De Bruijn WC; Fernandes J; Huber J; Koster JF Pathol Eur; 1975; 10(1):3-15. PubMed ID: 170575 [No Abstract] [Full Text] [Related]