R.D. Jolly was project leader who conceived and managed the research and was principally responsible for writing. N.R. Marshall was responsible for management and clinical procedures involving the experimental dogs. A. Hartman was the radiologist who managed and interpreted the CT scans. K.M. Hemsley and L.K. Winner were responsible for the assays of SGSH enzyme. J. Marshall performed the statistical analyses.
Intracisternal enzyme replacement therapy in lysosomal storage diseases: dispersal pathways, regional enzyme concentrations and the effect of posttreatment posture
Article first published online: 9 SEP 2013
© 2012 Massey University. Neuropathology and Applied Neurobiology © 2012 British Neuropathological Society
Neuropathology and Applied Neurobiology
Volume 39, Issue 6, pages 681–692, October 2013
How to Cite
Jolly, R. D., Marshall, N. R., Marshall, J., Hartman, A., Hemsley, K. M. and Winner, L. K. (2013), Intracisternal enzyme replacement therapy in lysosomal storage diseases: dispersal pathways, regional enzyme concentrations and the effect of posttreatment posture. Neuropathology and Applied Neurobiology, 39: 681–692. doi: 10.1111/nan.12010
- Issue published online: 9 SEP 2013
- Article first published online: 9 SEP 2013
- Accepted manuscript online: 17 DEC 2012 08:54PM EST
- Manuscript Accepted: 10 DEC 2012
- Manuscript Received: 8 JUL 2012
- The Society for Mucopolysaccharide Diseases
- Lysosomal Storage Diseases New Zealand
- Palmerston North Medical Research Foundation
- Shire Human Genetic Therapies
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