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Molecular Genetics and Metabolism|October 22, 2003
Canavan disease: a monogenic trait with complex genomic interactionSankar Surendran, Kimberlee Michals-Matalon, Michael J Quast, et al.
Biochemical and Biophysical Research Communications|October 10, 2006
Hyaluronidase increases the biodistribution of acid alpha-1,4 glucosidase in the muscle of Pompe disease mice: an approach to enhance the efficacy of enzyme replacement therapyReuben Matalon, Sankar Surendran, Gerald A Campbell, et al.
American Journal of Medical Genetics|November 29, 2002
DOOR syndrome: deficiency of E1 component of the 2-oxoglutarate dehydrogenase complexSankar Surendran, Kimberlee Michals-Matalon, Stephan Krywawych, et al.
Genetic Testing|December 20, 2002
Founder mutation R245H of Sanfilippo syndrome type A in the Cayman IslandsPeter L Rady, Sankar Surendran, Ahn T Vu, et al.
Genetic Testing|July 14, 2007
Mutations in the regulatory domain of phenylalanine hydroxylase and response to tetrahydrobiopterinLin Wang, Sankar Surendran, Kimberlee Michals-Matalon, et al.
Brain Research. Developmental Brain Research|October 7, 2004
Mouse neural progenitor cells differentiate into oligodendrocytes in the brain of a knockout mouse model of Canavan diseaseSankar Surendran, Lamya S Shihabuddin, Jennifer Clarke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2004
Biopterin responsive phenylalanine hydroxylase deficiencyReuben Matalon, Richard Koch, Kimberlee Michals-Matalon, et al.
Brain Research Bulletin|August 12, 2003
Expression of glutamate transporter, GABRA6, serine proteinase inhibitor 2 and low levels of glutamate and GABA in the brain of knock-out mouse for Canavan diseaseSankar Surendran, Peter L Rady, Kimberlee Michals-Matalon, et al.
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