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1
Enzyme loading of erythrocytes.
Proc Natl Acad Sci U S A. 1973 Sep;70(9):2663-6. doi: 10.1073/pnas.70.9.2663.
2
Effect of glutaraldehyde treatment on enzyme-loaded erythrocytes.
Biochim Biophys Acta. 1977 Feb 28;496(2):507-15. doi: 10.1016/0304-4165(77)90332-4.
4
A dialysis procedure for loading erythrocytes with enzymes and lipids.
Biochim Biophys Acta. 1977 Jan 24;496(1):136-45. doi: 10.1016/0304-4165(77)90121-0.
5
Editorial: Therapy in genetic disease.
N Engl J Med. 1974 Nov 7;291(19):1028-9. doi: 10.1056/NEJM197411072911910.
6
Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease.
N Engl J Med. 1974 Nov 7;291(19):989-93. doi: 10.1056/NEJM197411072911901.
7
A rapid micro assay method for amylo-1,6-glucosidase.
Anal Biochem. 1970 Jan;33(1):87-101. doi: 10.1016/0003-2697(70)90442-2.
8
Renal transplantation in Type II Gaucher disease.
Birth Defects Orig Artic Ser. 1973 Mar;9(2):109-19.
10
Neuropathic Gaucher's disease with normal 4-methylumbelliferyl-beta-glucosidase activity in the liver.
Pediatr Res. 1977 May;11(5):641-6. doi: 10.1203/00006450-197705000-00004.

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Protein measurement with the Folin phenol reagent.
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Accumulation of dextran in human red cells after haemolysis.
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Physiological characteristics of human red blood cell ghosts.
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Entry of ferritin into human red cells during hypotonic haemolysis.
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Destruction of injured red cells in vivo.
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L-asparaginase: therapeutic and toxic effects in patients with neoplastic disease.
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Composition of the membranous deposits occurring in Gaucher's disease.
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