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Gaucher's disease: Lack of antibody response to intravenous glucocerebrosidase

โœ Scribed by D.E. Britton; P.O. Leinikki; J.A. Barranger; R.O. Brady


Book ID
118938340
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
144 KB
Volume
23
Category
Article
ISSN
0024-3205

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We prospectively evaluated the clinical and biochemical responses to enzyme-replacement therapy (ERT) with macrophage-targeted glucocerebrosidase (Ceredase) infusions in 5 patients (age, 3.5-8.5 years) with type 3 Gaucher's disease. The patients were followed for up to 5 years. Enzyme dosage ranged