Progressive Myoclonus Epilepsy as an Inborn Error of Metabolism Comparable to Storage Disease
- 1 December 1963
- Vol. 4 (1-4) , 120-137
- https://doi.org/10.1111/j.1528-1157.1963.tb05215.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Progressive Myoclonus Epilepsy with Lafora Bodies. Clinical‐Pathological FeaturesEpilepsia, 1963
- Amaurotic Idiocy and EpilepsyEpilepsia, 1963
- ON THE DIFFERING APPEARANCE OF INTRANUCLEAR AND CYTOPLASMIC GLYCOGEN IN LIVER CELLS IN GLYCOGEN STORAGE DISEASEThe Journal of cell biology, 1962
- ENZYME LOCALIZATION IN RABBIT CEREBELLUM AND EFFECT OF POST MORTEM AUTOLYSIS*Journal of Neurochemistry, 1962
- DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE*Journal of Clinical Investigation, 1961
- A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASEJournal of Neurology, Neurosurgery & Psychiatry, 1960
- Serum Mucoproteins in Progressive Familial Myoclonic Epilepsy (A Preliminary Note)Epilepsia, 1959
- THE VALIDATION OF THE QUANTITATIVE HISTOCHEMICAL METHOD FOR USE ON POST MORTEM MATERIAL—IIJournal of Neurochemistry, 1958
- Histochemische Untersuchungen über die „basophile Substanz“ der Skeletmuskulatur bei GlykogenoseVirchows Archiv, 1958
- PROGRESSIVE FAMILIAL MYOCLONIC EPILEPSY IN THREE FAMILIES: ITS CLINICAL FEATURES AND PATHOLOGICAL BASIS: AN APPENDIX ON THE GENETIC ASPECTSBrain, 1955