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Betty Korljan Jelaska, Sanja Baršić Ostojić, Nina Berović, and Višnja Kokić

Background Glycogen storage disease (GSD) type Ia (von Gierke's disease) is an inherited (autosomal recessive transmission) metabolic disorder of glycogen metabolism, caused by the deficiency of glucose-6-phosphatase (G6P) (1) . G6P is an

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Takashi Matsuo and Yoshihiko Ushiroda

Cornblath M Dwyer AJ Adams AJ Girton ME Sidbury J 1982 Computed tomography of the liver and kidneys in glycogen storage disease . Journal of Computer Assisted Tomography 6 67 – 71 . ( doi:10.1097/00004728-198202000-00009 ) 29

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Tohru Eguchi and Shozo Miyauchi

exercising muscle. Second, hypokalemia has been shown to suppress the synthesis and storage of glycogen, an intracellular store of energy substrate for the exercising muscle. Finally, deranged ion transport across the cell membrane has been demonstrated (10