1. Aspartylglucosaminuria—an inborn error of metabolism associated with mental defect;Pollitt;Lancet,1968
2. Eleven new cases of aspartylglucosaminuria;Palo;J Ment Defic Res,1970
3. Aspartylglucosaminuria—analysis of thirty-four patients;Autio;J Ment Defic Res. Monograph Series I,1972
4. Thin-layer chromatographic demonstration of aspartylglycosylamine and a novel acidic carbohydrate in human tissues;Palo;J Chromatogr,1972
5. Isenberg JN, and Sharp HL: Aspartylglucosaminuria:biochemical and ultrastructural characteristics unique to this visceral storage disease. Accepted for publication.