The change in the ph 4 and ph 6 forms of α-glucosidase in cultured amniotic fluid cells and its implication in prenatal diagnosis of Pompe's disease
- 1 December 1978
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 90 (2) , 157-161
- https://doi.org/10.1016/0009-8981(78)90517-x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- A micro-radiochemical assay for α-1,4-glucosidase and its use in the assessment of type II glycogenosis (pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Two alpha-glucosidases in cultured amniotic fluid cells and their differentiation in the prenatal diagnosis of Pompe's diseaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Prenatal Diagnosis of Type II Glycogenosis (Pompe's Disease) Using Microchemical AnalysesPediatric Research, 1975
- A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Acid α-glucosidase in amniotic fluidBiochemical Medicine, 1973
- Alpha-1,4 glucosidase activity in Pompe's diseaseThe Journal of Pediatrics, 1971
- Intrauterine diagnosis and management of genetic defectsAmerican Journal of Obstetrics and Gynecology, 1967
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963