An improved method for the identification of patients and carriers of krabbe's disease
- 1 October 1974
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 56 (2), 199-206
- https://doi.org/10.1016/0009-8981(74)90228-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Deficiency of monogalactosyl diglyceride β-galactosidase activity in Krabbe's diseaseBiochemical and Biophysical Research Communications, 1973
- Galactocerebrosidase Deficiency in Globoid Cell Leucodystrophy of Late OnsetArchives of Disease in Childhood, 1972
- In utero diagnosis of globoid cell leukodystrophy (Krabbe's disease)Biochemical and Biophysical Research Communications, 1971
- Krabbe's Globoid Cell Leukodystrophy: Deficiency of Galactocerebrosidase in Serum, Leukocytes, and FibroblastsScience, 1971
- Globoid cell leukodystrophy (Krabbe's disease): isolation of myelin with normal glycolipid compositionJournal of Lipid Research, 1970
- Krabbe's leucodystrophy: Some clinical, genetic and pathogenetic considerationsJournal of the Neurological Sciences, 1970
- Studies on the Fibrinogen, Dextran and Phytohemagglutinin Methods of Isolating LeukocytesBlood, 1956
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951