A LIPID METABOLIC DISEASE —“MEMBRANOUS LIPODYSTROPHY”— AN AUTOPSY CASE DEMONSTRATING NUMEROUS PECULIAR MEMBRANE‐STRUCTURES COMPOSED OF COMPOUND LIPID IN BONE AND BONE MARROW AND VARIOUS ADIPOSE TISSUES
- 1 August 1973
- journal article
- Published by Wiley in Acta Pathologica Japonica
- Vol. 23 (3) , 539-558
- https://doi.org/10.1111/j.1440-1827.1973.tb01223.x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.Proceedings of the National Academy of Sciences, 1968
- Ceramide and Ganglioside Accumulation in Farber's Lipogranulomatosis.Experimental Biology and Medicine, 1967
- Leukodystrophie mit orthochromatischen AbbaustoffenVirchows Archiv, 1965
- Farber's disease: Report of a case with observations on its histogenesis and notes on the nature of the stored materialThe Journal of Pediatrics, 1962
- Über die nichtmetachromatischen LeukodystrophienArchiv Fur Psychiatrie Und Nervenkrankheiten, 1959
- Über die metachromatischen Leukodystrophien (Typ Scholz)Archiv Fur Psychiatrie Und Nervenkrankheiten, 1959
- NATURAL HISTORY AND EVOLUTION OF THE CONCEPT OF SCHILDER'S DIFFUSE SCLEROSISActa Psychiatrica Scandinavica, 1956
- GARGOYLISM (LIPOCHONDRODYSTROPHY)American Journal of Diseases of Children, 1948
- Das apallische SyndromZeitschrift für die gesamte Neurologie und Psychiatrie, 1940
- Some Problems of Pathogenesis in Schilder's DiseaseJournal of Mental Science, 1936