Studies on neurotransmitter markers and neuronal cell density in the cerebellar system in olivopontocerebellar atrophy and cortical cerebellar atrophy

1985 ◽  
Vol 71 (2-3) ◽  
pp. 193-208 ◽  
Author(s):  
Ichiro Kanazawa ◽  
Shin Kwak ◽  
Hidenao Sasaki ◽  
Hidehiro Mizusawa ◽  
Osamu Muramoto ◽  
...  
Author(s):  
Mario Mascalchi

MRI shows in-vivo the three archetypal patterns of CNS volume loss underlying progressive ataxias, namely spinal atrophy (SA), cortical cerebellar atrophy (CCA) and olivopontocerebellar atrophy (OPCA). The MRI-based CNS atrophy pattern was reviewed in 128 progressive ataxias. A CNS atrophy pattern was identified in 91 conditions: SA in Freidreich’s ataxia, CCA in 5 acquired and 72 (24 dominant, 47 recessive,1 X-linked) inherited ataxias, OPCA in Multi-System Atrophy and 12 (9 dominant, 2 recessive,1 X-linked) inherited ataxias. The MRI-based CNS atrophy pattern may be useful for genetic assessment, identification of shared cellular targets, and repurposing therapies or enlargement of drugs indications in progressive ataxias.


2003 ◽  
Vol 114 (4) ◽  
pp. 740-747 ◽  
Author(s):  
Mio Arai ◽  
Hideaki Tanaka ◽  
Roberto D Pascual-Marqui ◽  
Koichi Hirata

2015 ◽  
Vol 54 (14) ◽  
pp. 1717-1723 ◽  
Author(s):  
Yusuke Fukui ◽  
Nozomi Hishikawa ◽  
Kota Sato ◽  
Syoichiro Kono ◽  
Kosuke Matsuzono ◽  
...  

1946 ◽  
Vol 5 (1) ◽  
pp. 29-42 ◽  
Author(s):  
Ben W. Lichtenstein ◽  
Samuel A. Levinson

Brain ◽  
1933 ◽  
Vol 56 (2) ◽  
pp. 191-212 ◽  
Author(s):  
H. L. PARKER ◽  
J. W. KERNOHAN

1994 ◽  
Vol 103 (2) ◽  
pp. 98-104 ◽  
Author(s):  
Hermann Ackermann ◽  
Wolfram Ziegler

Acoustic analysis of vocal instability during the production of isolated vowels, including computation of mean fundamental frequency (F0), period-to-period variability (jitter), pitch fluctuations, and between-trial variation of F0, was performed in 20 patients with cerebellar cortical dysfunction. Eleven subjects suffered from purely cerebellar atrophy (CA). In the remaining 9 patients olivopontocerebellar atrophy (OPCA) had been diagnosed. A subgroup of both the CA and OPCA subjects presented with enlarged pitch fluctuations and/or increased jitter values. It is conceivable that asymmetrically distributed motor deficits at the laryngeal level and altered gain settings of laryngeal and/or respiratory reflexes account for the observed phonatory instability. Moreover, 5 of the 20 cerebellar patients had a pitch level exceeding the upper limit of the normal range. Presumably, this deviation reflects increased vocal effort.


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