Archives of Neurology · 1980 · 19 citations · 14 references
MedicineNeurologyPathologyHepatologyMolecular PathologyNeuropathologyCarbohydrate Metabolism DisordersGenetic DisordersLysosomal Storage DisordersDisorders Of GlyconeogenesisGaucher DiseaseInherited Disorders Of Glycolipid MetabolismNeurologic Deficits
We discuss the clinical features of two patients with type 3 Gaucher's disease. Glucocerebroside levels in liver biopsy specimens were measured in both patients and the findings are discussed in regard to the pathogenesis of the disease.
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Replacement Therapy for Inherited Enzyme Deficiency
Roscoe O. Brady, John F. Tallman, William G. Johnson et al. · New England Journal of Medicine · 1973 · 309 citations
Replacement Therapy for Inherited Enzyme Deficiency
Roscoe O. Brady, Peter G. Pentchev, Andrew E. Gal et al. · New England Journal of Medicine · 1974 · 294 citations
Diagnosis of Gaucher's Disease and Niemann-Pick Disease with Small Samples of Venous Blood
John P. Kampine, Roscoe O. Bardy, Julian N. Kanfer et al. · Science · 1967 · 288 citations