N-acetyl-β-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses
- 1 May 1977
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 76 (3), 309-315
- https://doi.org/10.1016/0009-8981(77)90156-5
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Inutero diagnosis of Sandhoff's diseaseBiochemical and Biophysical Research Communications, 1973
- Separation and characterisation of N-acetyl-β-glucosaminidases A and P from maternal serumBiochimica et Biophysica Acta (BBA) - Protein Structure, 1972
- Tay-Sachs Disease: Prenatal DiagnosisScience, 1971
- Electrophoretic characterization of glucose dehydrogenase, β-glucuronidase, and N-acetyl-β-glucosaminidase from placenta and gestational serumAmerican Journal of Obstetrics and Gynecology, 1971
- PRENATAL DIAGNOSIS OF TAY-SACHS DISEASEThe Lancet, 1970
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969
- Comparative Study of the Rh-D Antibody Titres of Amniotic Fluids and Corresponding Maternal Sera in Rh-D Sensitized PregnanciesNature, 1969
- N-Acetyl-β-glucosaminidases in human spleenBiochemical Journal, 1968
- Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organsLife Sciences, 1968
- DISC ELECTROPHORESIS – II METHOD AND APPLICATION TO HUMAN SERUM PROTEINS*Annals of the New York Academy of Sciences, 1964