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- W2014223119 abstract "BackgroundGaucher disease (GD) is a rare lysosomal storage disease caused by deficiency in the enzyme beta-glucocerebrosidase. Along with visceral, hematologic, and bone manifestations, patients may experience chronic fatigue resulting in functional disability and reduced quality of life. Management of the disease includes therapeutic intervention, supportive therapies, and regular monitoring of all clinically relevant disease signs and symptoms. However, current practice guidelines do not include measurement of fatigue or therapeutic goals for fatigue." @default.
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- W2014223119 date "2014-02-01" @default.
- W2014223119 modified "2023-09-23" @default.
- W2014223119 title "Rethinking fatigue in Gaucher disease" @default.
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