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Muscle & Nerve|October 29, 2002
Physiological characterization of neuropathy in Fabry's diseaseCarlos A Luciano, James W Russell, Tapas K Banerjee, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 2000
Long-term enzyme correction and lipid reduction in multiple organs of primary and secondary transplanted Fabry mice receiving transduced bone marrow cellsT Takenaka, G J Murray, G Qin, et al.
Biochimica Et Biophysica Acta|September 8, 1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidaseP G Pentchev, A E Gal, A D Booth, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Niemann-pick variant disorders: comparison of errors of cellular cholesterol homeostasis in group D and group C fibroblastsJ D Butler, M E Comly, H S Kruth, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1987
Group C Niemann-Pick disease: faulty regulation of low-density lipoprotein uptake and cholesterol storage in cultured fibroblastsP G Pentchev, M E Comly, H S Kruth, et al.
The Journal of Endocrinology|March 10, 2016
Increased plasma leptin attenuates adaptive metabolism in early lactating dairy cowsRichard A Ehrhardt, Andreas Foskolos, Sarah L Giesy, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
alpha-Galactosidase A deficient mice: a model of Fabry diseaseT Ohshima, G J Murray, W D Swaim, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 1999
Aging accentuates and bone marrow transplantation ameliorates metabolic defects in Fabry disease miceT Ohshima, R Schiffmann, G J Murray, et al.
Pediatrics|February 17, 2005
Pediatric Fabry diseaseMarkus Ries, Surya Gupta, David F Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry diseaseR Schiffmann, G J Murray, D Treco, et al.
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