scholarly journals Syntactic Comprehension in Patients with Amyotrophic Lateral Sclerosis

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Kentarou Yoshizawa ◽  
Nao Yasuda ◽  
Michinari Fukuda ◽  
Yumi Yukimoto ◽  
Mieko Ogino ◽  
...  

Recent neuropsychological studies of patients with amyotrophic lateral sclerosis (ALS) have demonstrated that some patients have aphasic symptoms, including impaired syntactic comprehension. However, it is not known if syntactic comprehension disorder is related to executive and visuospatial dysfunction. In this study, we evaluated syntactic comprehension using the Syntax Test for Aphasia (STA) auditory comprehension task, frontal executive function using the Frontal Assessment Battery (FAB), visuospatial function using Raven’s Coloured Progressive Matrices (RCPM), and dementia using the Hasegawa Dementia Scale-Revised (HDS-R) in 25 patients with ALS. Of the 25 patients, 18 (72%) had syntactic comprehension disorder (STA score < IV), nine (36%) had frontal executive dysfunction (FAB score < 14), six (24%) had visuospatial dysfunction (RCPM score < 24), and none had dementia (HDS-R score < 20). Nine of the 18 patients with syntactic comprehension disorder (50%) passed the FAB and RCPM. Although sample size was small, these patients had a low STA score but normal FAB and RCPM score. All patients with bulbar onset ALS had syntactic comprehension disorder. These results indicate that it might be necessary to assess syntactic comprehension in patients with bulbar onset ALS. The implications of these findings are discussed in relation to the pathological continuum of ALS.

2010 ◽  
Vol 11 (1-2) ◽  
pp. 244-247 ◽  
Author(s):  
Björn Oskarsson ◽  
Dianna Quan ◽  
Yvonne D. Rollins ◽  
Hans E. Neville ◽  
Steven P. Ringel ◽  
...  

2017 ◽  
Vol 7 (6) ◽  
pp. e00707 ◽  
Author(s):  
Tatsuhiro Terada ◽  
Jun Miyata ◽  
Tomokazu Obi ◽  
Manabu Kubota ◽  
Miho Yoshizumi ◽  
...  

2021 ◽  
Vol 11 (7) ◽  
pp. 906
Author(s):  
Nimeshan Geevasinga ◽  
Mehdi Van den Bos ◽  
Parvathi Menon ◽  
Steve Vucic

Amyotrophic lateral sclerosis (ALS) is characterised by progressive dysfunction of the upper and lower motor neurons. The disease can evolve over time from focal limb or bulbar onset to involvement of other regions. There is some clinical heterogeneity in ALS with various phenotypes of the disease described, from primary lateral sclerosis, progressive muscular atrophy and flail arm/leg phenotypes. Whilst the majority of ALS patients are sporadic in nature, recent advances have highlighted genetic forms of the disease. Given the close relationship between ALS and frontotemporal dementia, the importance of cortical dysfunction has gained prominence. Transcranial magnetic stimulation (TMS) is a noninvasive neurophysiological tool to explore the function of the motor cortex and thereby cortical excitability. In this review, we highlight the utility of TMS and explore cortical excitability in ALS diagnosis, pathogenesis and insights gained from genetic and variant forms of the disease.


2016 ◽  
Vol 38 (3) ◽  
pp. 1249-1268 ◽  
Author(s):  
Dennis Dimond ◽  
Abdullah Ishaque ◽  
Sneha Chenji ◽  
Dennell Mah ◽  
Zhang Chen ◽  
...  

2012 ◽  
Vol 27 (3) ◽  
pp. 348-354 ◽  
Author(s):  
I. Zalonis ◽  
F. Christidi ◽  
G. Paraskevas ◽  
T. Zabelis ◽  
I. Evdokimidis ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document