Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference55 articles.
1. Andreassen OA, Ferrante RJ, Klivenyi P, Klein AM, Shinobu LA, Epstein CJ, Beal MF (2000) Partial deficiency of manganese superoxide dismutase exacerbates a transgenic mouse model of amyotrophic lateral sclerosis. Ann Neurol 47: 447–455
2. Andrews TC, Weeks RA, Turjanski N, Brooks DJ (1998) Monitoring disease progression in presymptomatic and early Huntington’s disease: D1 and D2 ligand PET and the unified Huntington’s rating scale. Neurology (suppl. 1) A 348
3. Andrus PK, Fleck TJ, Gurney ME, Hall ED (1998) Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis. J Neurochem 71: 2041–2048
4. Antonini A, Leenders K, Eidelberg D (1998) (11C) Raclopride PET studies of the Huntington’s disease rate of progression: relevance of the trinucleotide repeat length. Ann Neurol 43: 253–255
5. Azzouz M, Leclerc N, Gurney M, Warter J-M, Poindron P, Borg J (1997) Progressive motor neuron impairment in an animal model of familial amy-atrophic lateral sclerosis. Muscle Nerve 20: 45–51
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