The absence of unique kainic acid-like molecules in urine, serum, and CSF from Huntington's disease patients
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference17 articles.
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3. Ontogenetic development of kainate neurotoxicity — Correlates with glutamatergic innervation;Campochiaro,1978
4. Lesion of striatal neurons with kainic acid provides a model for Huntington's chorea;Coyle;Nature (Lond.),1976
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1. Biofluid Biomarkers in Huntington’s Disease;Methods in Molecular Biology;2018
2. Chronic intrastriatal -pyroglutamate: Neuropathology and neuron sparing like Huntington's disease;Experimental Neurology;1989-05
3. Excitotoxins and Animal “Models” of Human Disease;Recent Advances in Nervous System Toxicology;1988
4. ASTROCYTES IN HUNTINGTON'S CHOREA;Astrocytes;1986
5. Quinolinic acid and other kynurenines in the central nervous system;Neuroscience;1985-07
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