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Science (New York, N.Y.)|February 25, 1972
Isozymes of phenylalanine hydroxylaseJ A Barranger, P J Geiger, A Huzino, et al.
The Journal of Clinical Investigation|November 1, 1981
Selective effects of glucocerebroside (Gaucher's storage material) on macrophage culturesI Gery, J S Zigler, R O Brady, et al.
Ophthalmic Paediatrics and Genetics|April 1, 1984
The pathology of pingueculae in Gaucher's diseaseF C Chu, M M Rodrigues, D G Cogan, et al.
Gene Therapy|February 24, 1998
The effect of cationic liposome pretreatment and centrifugation on retrovirus-mediated gene transferW P Swaney, F L Sorgi, A B Bahnson, et al.
Biochimica Et Biophysica Acta|April 3, 1981
Uptake and distribution of placental glucocerebrosidase in rat hepatic cells and effects of sequential deglycosylationF S Furbish, C J Steer, N L Krett, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1983
Macula halo syndrome. Variant of Niemann-Pick diseaseD G Cogan, F C Chu, J A Barranger, et al.
Medicine|September 1, 1985
Skeletal complications of Gaucher diseaseD W Stowens, S L Teitelbaum, A J Kahn, et al.
Annals of Neurology|August 1, 1986
Type 2 and type 3 Gaucher disease: a morphological and biochemical studyE M Kaye, M D Ullman, E R Wilson, et al.
Gene Therapy|July 1, 1994
Expression of the human glucocerebrosidase and arylsulfatase A genes in murine and patient primary fibroblasts transduced by an adeno-associated virus vectorJ F Wei, F S Wei, R J Samulski, et al.
Progress in Clinical and Biological Research|January 1, 1982
Gaucher disease: hepatic abnormalities in 25 patientsS P James, F W Stromeyer, D W Stowens, et al.
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