Clinical neurophysiology of ALS

被引:67
作者
Eisen, A
Swash, M
机构
[1] Vancouver Gen Hosp, Neuromuscular Dis Unit, Vancouver, BC V5Z 1M9, Canada
[2] Queen Mary Univ London, Barts & London Sch Med & Dent, London E1 4NS, England
关键词
amyotrophic lateral sclerosis; neurophysiology; motor unit number estimation; transcranial magnetic stimulation; reviews;
D O I
10.1016/S1388-2457(01)00692-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The neurophysiology of amyotrophic lateral sclerosis is important not only in relation to diagnosis, but also in the development of methods to follow progress, and the effects of Putative therapies. in the disease. Quantitative techniques can he applied to the measurement of reinnervation using needle electromyogram. The methodology of motor unit number estimation may be useful in measuring loss of functioning motor units in groups, of patients but variability in the measurement using current methods limits its sensitivity in the evaluation of individual patients. Conventional neurophysiological measurements. expressed as a multimetric index. may be useful in assessing progress. The cortical and upper motor neuron system can be assessed using transcortical magnetic stimulation protocols, and cortical excitability may be measured by the peristimulus histogram method. In this review the advantages. limitations and promise of these various methods is discussed. in order to indicate the direction for further neurophysiological studies in this disorder. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:2190 / 2201
页数:12
相关论文
共 162 条
[1]   Effect of noninvasive positive-pressure ventilation on survival in amyotrophic lateral sclerosis [J].
Aboussouan, LS ;
Khan, SU ;
Meeker, DP ;
Stelmach, K ;
Mitsumoto, H .
ANNALS OF INTERNAL MEDICINE, 1997, 127 (06) :450-453
[2]   Evolution of motor and sensory deficits in amyotrophic lateral sclerosis estimated by neurophysiological techniques [J].
Al Theys, P ;
Peeters, E ;
Robberecht, W .
JOURNAL OF NEUROLOGY, 1999, 246 (06) :438-442
[3]  
Al-Chalabi Ammar, 2000, Current Opinion in Neurology, V13, P397, DOI 10.1097/00019052-200008000-00006
[4]  
Andersen Kjeld V., 1999, Tidsskrift for den Norske Laegeforening, V119, P1591
[5]   Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation - A clinical and genealogical study of 36 patients [J].
Andersen, PM ;
Forsgren, L ;
Binzer, M ;
Nilsson, P ;
AlaHurula, V ;
Keranen, ML ;
Bergmark, L ;
Saarinen, A ;
Haltia, T ;
Tarvainen, I ;
Kinnunen, E ;
Udd, B ;
Marklund, SL .
BRAIN, 1996, 119 :1153-1172
[6]  
Andersen PM, 2001, AMYOTROPH LATERAL SC, V2, pS37
[7]  
ANDERSEN PM, 1997, AMYOTROPHIC LATERAL
[8]   USE OF COMPOSITE SCORES (MEGASCORES) TO MEASURE DEFICIT IN AMYOTROPHIC LATERAL SCLEROSIS [J].
ANDRES, PL ;
FINISON, LJ ;
CONLON, T ;
THIBODEAU, LM ;
MUNSAT, TL .
NEUROLOGY, 1988, 38 (03) :405-408
[9]  
[Anonymous], 1998, AMYOTROPHIC LATERAL
[10]   INTRAFAMILIAL HETEROGENEITY IN HEREDITARY MOTOR-NEURON DISEASE [J].
APPELBAUM, JS ;
ROOS, RP ;
SALAZARGRUESO, EF ;
BUCHMAN, A ;
IANNACCONE, S ;
GLANTZ, R ;
SIDDIQUE, T ;
MASELLI, R .
NEUROLOGY, 1992, 42 (08) :1488-1492