Huntington's disease, energy, and excitotoxicity-Reference-Cited by-同舟云学术

Huntington's disease, energy, and excitotoxicity

Published:1994-03 Issue:2 Volume:15 Page:275-276
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Flint Beal M.

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference13 articles.

1. Alternative excitotoxic hypothesis;Albin;Neurology,1992

2. Beal, M. F.; Brouillet, E.; Jenkins, B.; Rosen, B.; Srivastava, R.; Hyman, B. T. Age-dependent neurotoxicity of the mitochondrial toxin 3-nitropropionic acid Ann. Neurol. (in press).

3. Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid;Beal;Nature,1986

4. Quinolinic acid striatal lesions in primates as a model of Huntington's disease;Beal;Ann. Neurol.,1989

5. Aminooxyacetic acid results in excitotoxin lesions by a novel indirect mechanism;Beal;J. Neurochem.,1991

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