1. The mucopolysaccharide storage diseases;McKusick, V.A.; Neufeld, E.F.,1983
2. Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5'-diphosphate-N-acetylglucosamine. Glycoprotein N-acetylglycosaminylphosphotransferase activity;Reitman, M.L.; Varki, A.; Kornfeld, S.;J Clin Invest,1981
3. Mucolipidosis III (pseudo-Hurler polydystrophy): clinical and laboratory studies in a series of 12 patients;Kelly, T.E.; Thomas, G.H.; Taylor, H.A.;The3ohns Hopkins Medical Journal,1975
4. Carpal tunnel syndrome and trigger finger in childhood;McArthur, R.G.; Hayles, A.B.; Gomez, M.R.; Bianco, A.J.;AmJ Dis Child
5. The hand in mucopolysaccharide disorders;Fisher, R.C.; Horner, R.L.; Wood, V.E.;Clin Orthop,1974