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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. [Genetic heterogeneity and the diagnosis of hepatic glycogenoses]. Lemonnier A; Baussan C; Moatti N C R Seances Soc Biol Fil; 1984; 178(4):327-47. PubMed ID: 6241011 [TBL] [Abstract][Full Text] [Related]
7. [Hereditary defects of glycogenolysis and glycolysis enzymes in neuromuscular diseases (a review)]. Rozenfel'd EL; Popova IA Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):115-22. PubMed ID: 2851906 [No Abstract] [Full Text] [Related]
8. [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]
9. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation. Iwamasa T; Ninomiya N; Fukuda S; Hamada T; Hirashima M; Osame M Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. [The pre- and posttranslational regulation of the enzymes participating in glycogen phosphorolysis]. Parsadanian GK; Marchenko SN Tsitol Genet; 1993; 27(6):64-78. PubMed ID: 8066810 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Animal models of glycogen storage conditions. Their relation to human disease. Gross SR West J Med; 1975 Sep; 123(3):194-201. PubMed ID: 1099809 [No Abstract] [Full Text] [Related] [Next] [New Search]