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2. [A case of glycogen storage myopathy with acute heart failure]. Nakamura Y; Takahashi M; Maeda M; Yamada Y; Kono N Rinsho Shinkeigaku; 1990 May; 30(5):524-8. PubMed ID: 2205434 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. [Clinical and biochemical correlations in certain metabolic myopathies]. de Barsy T Bull Mem Acad R Med Belg; 1992; 147(10):385-92; discussion 392-3. PubMed ID: 1303789 [TBL] [Abstract][Full Text] [Related]
5. Characterization of the glycolysis in lactate dehydrogenase-A deficiency. Miyajima H; Takahashi Y; Kaneko E Muscle Nerve; 1995 Aug; 18(8):874-8. PubMed ID: 7630349 [TBL] [Abstract][Full Text] [Related]
6. [Determination of blood level of muscle enzymes in glycogenoses with liver involvement: a diagnostic criterion]. Labrune P; Chalas J; Pignon JP; Hennion C; Odièvre M Ann Pediatr (Paris); 1989 May; 36(5):299-301. PubMed ID: 2742313 [TBL] [Abstract][Full Text] [Related]
7. Creatine kinase and lactate dehydrogenase in type 2 glycogenosis (Pompe disease). Gerson B; Hemphill JM; Rock RC Arch Pathol Lab Med; 1977 Apr; 101(4):213-5. PubMed ID: 265697 [TBL] [Abstract][Full Text] [Related]
8. [Study of human muscle biopsies with muscle glycogen storage diseases using 1H nuclear magnetic resonance spectroscopy (NMRS)--analysis of perchloric acid extracts of muscles]. Sugie H; Sugie Y; Ito M; Tsurui S Rinsho Shinkeigaku; 1991 Jun; 31(6):616-8. PubMed ID: 1657479 [TBL] [Abstract][Full Text] [Related]
9. [A case of glycogen storage disease with normal acid maltase accompanied with the abnormal platelet function]. Katsumi Y; Tokonami F; Matsui M; Aii H; Nonaka I Rinsho Shinkeigaku; 1994 Aug; 34(8):827-31. PubMed ID: 7994992 [TBL] [Abstract][Full Text] [Related]
10. [Biochemistry of striated muscle in the course of human muscular diseases]. Schapira G; Schapira F; Dreyfus JC Z Klin Chem Klin Biochem; 1967 Sep; 5(5):241-4. PubMed ID: 5272293 [No Abstract] [Full Text] [Related]
11. Lactate and phosphagen concentrations in working muscle of man with special reference to oxygen deficit at the onset of work. Karlsson J Acta Physiol Scand Suppl; 1971; 358():1-72. PubMed ID: 5549478 [No Abstract] [Full Text] [Related]
12. [A 21-year-old man with distal dominant progressive muscle atrophy]. Hattori Y; Nohara C; Hirasawa E; Mori H; Imai H; Mizuno Y No To Shinkei; 1995 May; 47(5):509-18. PubMed ID: 7786629 [TBL] [Abstract][Full Text] [Related]
13. [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]
14. Proglycogen, macroglycogen, glucose, and glucose-6-phosphate concentrations in skeletal muscles of horses with polysaccharide storage myopathy performing light exercise. Bröjer JT; Essén-Gustavsson B; Annandale EJ; Valberg SJ Am J Vet Res; 2006 Sep; 67(9):1589-94. PubMed ID: 16948606 [TBL] [Abstract][Full Text] [Related]
15. Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease). Witzleben CL Lab Invest; 1969 May; 20(5):424-9. PubMed ID: 4305720 [No Abstract] [Full Text] [Related]
16. Study of skeletal muscle glycogenolysis and glycolysis in chronic steroid myopathy, non-steroid histochemical type-2 fiber atrophy, and denervation. Danon MJ; Schliselfeld LH Clin Biochem; 2007 Jan; 40(1-2):46-51. PubMed ID: 17054931 [TBL] [Abstract][Full Text] [Related]