The absence of unique kainic acid-like molecules in urine, serum, and CSF from Huntington's disease patients
- 30 September 1981
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 51 (3) , 355-360
- https://doi.org/10.1016/0022-510x(81)90113-1
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Glutaric acidemiaNeurology, 1980
- ACTION OF THE NEUROTOXIN KAINIC ACID ON HIGH AFFINITY UPTAKE OF l‐GLUTAMIC ACID IN RAT BRAIN SLICESJournal of Neurochemistry, 1979
- Structure-activity relations for the neurotoxicity of kainic acid derivatives and glutamate analoguesNeuropharmacology, 1978
- Sulfite Oxidase DeficiencyNew England Journal of Medicine, 1977
- Scanning electron microscopy studies of erythrocytes in Huntington's DiseaseBiochemical and Biophysical Research Communications, 1977
- Electron spin resonance study of membrane protein alterations in erythrocytes in Huntington's diseaseNature, 1977
- Clinical, neuropathologic and pharmacologic aspects of Huntington's disease: Correlates with a new animal modelProgress in Neuro-Psychopharmacology, 1977
- Lesion of striatal neurons with kainic acid provides a model for Huntington's choreaNature, 1976
- d‐GLYCERIC‐ACIDAEMIA AND NON‐KETOTIC HYPERGLYCINEMIAActa Paediatrica, 1976