1. Infantile neuraminidase and l-galactosidase deficiencies (galactosialidosis) with mild clinical courses;Andria, G.; Strisciuglio, P.; Pontarelli, G.; Sly, W.S.; Dodson, W.E.,1981
2. Sialidosis: a review of human neuraminidase deficiency;Lowden, J.A.; O'Brien, J.S.;AmJHwn Genet,1979
3. Adult-type neuronal storage disease with neuraminidase deficiency;Miyatake, T.; Atsumi, T.; Obayashi, T.; Mizuno, Y.; Ando, S.; Ariga, T.;Ann Neurol,1979
4. Molecular defect in combined, B-galactosidase;d'Azzo A; A, Hoogeveen; AJJ, Reuser; D, Robinson; H, Galjaard,1982
5. Human placental neuraminidase: activation, stabilization and association with I-galactosidase and its 'protective' protein;Verheijen, F.W.; Palmeri, S.; Hoogeveen, A.T.; Galjaard, H.;EurJrBiochem,1985