Claudia Zuppaldi

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BACKGROUND Glycogen storage disease type 1 (GSD1) is a rare and genetically heterogeneous metabolic defect of gluconeogenesis due to mutations of either the G6PC gene (GSD1a) or the SLC37A4 gene (GSD1b). Osteopenia is a known complication of GSD1. OBJECTIVES The aim of this study was to investigate the effects of poor metabolic control and/or use of(More)
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