1. Prenatal diagnosis of type II glycogenosis (Pompe's disease) using michrochemical analyses;Niermeijer, M.F.; Koster, J.F.; Jahodova, M.; Fernandes, J.; Heukels-Dully, M.J.; Galjaard, H.;Paediatric Research,1975
2. Pranatale diagnose einer Glykogenose Typ II (Pompe) mit nachfolgender Interruptio;Schaub, J.; Osang, M.; von Bassewitz, D.B.; Grote, W.; Terinde, R.; Lombeck, I.; Bremer, H.J.;Deutsche Medizinishe Wochenschrift,1974
3. Faed for allowing us to study and report Case 2; Mr;thank Dr M, We
4. Mucopolysaccharidosis I has been classified on clinical grounds into three subtypes: MPS-IH (Hurler syndrome), MPS-IS (Scheie syndrome), and MPS-IH/S (Hurler-Scheie compound) (McKusick et al;Matalon, Cifonelli; Dorfman,1972
5. Material and methods Leucocytes were separated from 10 ml heparinized whole blood using dextran (Skoog and Beck, 1956). Fibroblasts were harvested on the seventh day of subculture. Assay of a-L-iduronidase employed 0.01 M phenyl-iduronide,* as previously described;Hall, and Neufeld (1968a, b).,1973