Fabry's disease (ceramide trihexosidase deficiency): Diagnostic confirmation by analysis of dental pulp
- 1 October 1972
- journal article
- Published by Elsevier in Archives of Oral Biology
- Vol. 17 (10) , 1473-IN13
- https://doi.org/10.1016/0003-9969(72)90107-0
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
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- Diagnosis of Glycosphingolipidoses by Urinary-Sediment AnalysisNew England Journal of Medicine, 1971
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- Fabry's Disease: Alpha-Galactosidase DeficiencyScience, 1970
- Tissue distribution of glycosphingolipids in a case of Fabry's diseaseJournal of Lipid Research, 1969
- Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosisJournal of Lipid Research, 1969
- The simultaneous estimation of 6-deoxy-l-galactose (l-fucose), d-mannose, d-galactose, 2-acetamido-2-deoxy-d-glucose (N-acetyl-d-glucosamine) and N-acetylneuraminic acid (sialic acid) in glycopeptides and glycoproteinsBiochimica et Biophysica Acta (BBA) - General Subjects, 1967
- Enzymatic Defect in Fabry's DiseaseNew England Journal of Medicine, 1967
- Pulpectomy as a diagnostic procedure in metachromatic leukodystrophyOral Surgery, Oral Medicine, Oral Pathology, 1967
- Biopsy of the Dental Pulp in the Diagnosis of Metachromatic LeucodystrophyDevelopmental Medicine and Child Neurology, 1965