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Journal of Neuropathology and Experimental Neurology|September 21, 2007
Developmental analysis of CNS pathology in the lysosomal storage disease alpha-mannosidosisAllison C Crawley, Steven U Walkley
Behavioural Brain Research|May 3, 2008
Open field locomotor activity and anxiety-related behaviors in mucopolysaccharidosis type IIIA miceAdeline A Lau, Allison C Crawley, John J Hopwood, et al.
Molecular Genetics and Metabolism|June 30, 2006
Enzyme replacement therapy in alpha-mannosidosis guinea-pigsAllison C Crawley, Barbara King, Thomas Berg, et al.
Molecular Genetics and Metabolism|March 22, 2003
Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapyDyane Auclair, John J Hopwood, Douglas A Brooks, et al.
Brain Research|July 11, 2006
Characterization of a C57BL/6 congenic mouse strain of mucopolysaccharidosis type IIIAAllison C Crawley, Briony L Gliddon, Dyane Auclair, et al.
The European Journal of Neuroscience|March 24, 2009
Examination of intravenous and intra-CSF protein delivery for treatment of neurological diseaseKim M Hemsley, Amanda J Luck, Allison C Crawley, et al.
Neurobiology of Disease|May 10, 2011
Enzyme replacement reduces neuropathology in MPS IIIA dogsAllison C Crawley, Neil Marshall, Helen Beard, et al.
Molecular Genetics and Metabolism|August 25, 2009
Effect of cisternal sulfamidase delivery in MPS IIIA Huntaway dogs--a proof of principle studyKim M Hemsley, Elizabeth J Norman, Allison C Crawley, et al.
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