Sporadic amyotrophic lateral sclerosis with multiple system degeneration: a report of an autopsy case without respirator administration

1999 ◽  
Vol 98 (5) ◽  
pp. 512-515 ◽  
Author(s):  
Y. Machida ◽  
K. Tsuchiya ◽  
M. Anno ◽  
C. Haga ◽  
T. Ito ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
System Degeneration ◽  
Multiple System Degeneration ◽  
Lateral Sclerosis

An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1mutation

2013 ◽  
Vol 34 (1) ◽  
pp. 58-63 ◽  
Author(s):  
Seika Nakamura ◽  
Reika Wate ◽  
Satoshi Kaneko ◽  
Hidefumi Ito ◽  
Mitsuaki Oki ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
Lateral Sclerosis

Widespread multiple system degeneration in a patient with familial amyotrophic lateral sclerosis

1993 ◽  
Vol 120 (1) ◽  
pp. 15-21 ◽  
Author(s):  
Hitoshi Takahashi ◽  
Kiyomitsu Oyanagi ◽  
Fusahiro Ikuta ◽  
Masami Tanaka ◽  
Tatsuhiko Yuasa ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Familial Amyotrophic Lateral Sclerosis ◽  
System Degeneration ◽  
Multiple System Degeneration ◽  
Lateral Sclerosis

Sporadic amyotrophic lateral sclerosis resembling primary lateral sclerosis: Report of an autopsy case and a review of the literature

1999 ◽  
Vol 19 (1) ◽  
pp. 71-76 ◽  
Author(s):  
Kuniaki Tsuchiya ◽  
Masanobu Arai ◽  
Shoji Matsuya ◽  
Hiroshi Nishimura ◽  
Toshitaka Ishiko ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Primary Lateral Sclerosis ◽  
Autopsy Case ◽  
Review Of The Literature ◽  
Primary Lateral ◽  
Lateral Sclerosis

Sporadic amyotrophic lateral sclerosis of long duration mimicking spinal progressive muscular atrophy exists: Additional autopsy case with a clinical course of 19 years

2004 ◽  
Vol 24 (3) ◽  
pp. 228-235 ◽  
Author(s):  
Kuniaki Tsuchiya ◽  
Michio Sano ◽  
Hidetoshi Shiotsu ◽  
Haruhiko Akiyama ◽  
Sadakiyo Watabiki ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Clinical Course ◽  
Muscular Atrophy ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
Long Duration ◽  
Lateral Sclerosis ◽  
Progressive Muscular Atrophy

Sporadic amyotrophic lateral sclerosis with circumscribed temporal atrophy: A report of an autopsy case without dementia and with ubiquitinated intraneuronal inclusions

2002 ◽  
Vol 22 (4) ◽  
pp. 308-316 ◽  
Author(s):  
Kuniaki Tsuchiya ◽  
Matuu Takahashi ◽  
Hidetoshi Shiotsu ◽  
Haruhiko Akiyama ◽  
Chie Haga ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
Lateral Sclerosis

An autopsy case of sporadic amyotrophic lateral sclerosis with 16-year survival without artificial ventilation

1999 ◽  
Vol 19 (1) ◽  
pp. 85-92 ◽  
Author(s):  
Yutaka Honma ◽  
Takashi Komori ◽  
Shuichi Kato ◽  
Nami Suda ◽  
Akira Kawata ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Artificial Ventilation ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Autopsy Case ◽  
Lateral Sclerosis

scholarly journals Glutathione S-transferase Omega 2 DD genotype is associated with an increased risk of sporadic amyotrophic lateral sclerosis in Chinese men

2021 ◽  
Vol 49 (7) ◽  
pp. 030006052110332
Author(s):  
Zhiliang Fan ◽  
Hong Jiang ◽  
Xueqin Song ◽  
Yansu Guo ◽  
Xinying Tian
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Healthy Subjects ◽  
Chinese Population ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Glutathione S Transferase ◽  
Genotype Frequencies ◽  
Sporadic Als ◽  
Increased Risk ◽  
Chi Squared ◽  
Lateral Sclerosis

Objective To investigate whether GSTA1, GSTO2, and GSTZ1 are relevant to an increased risk of amyotrophic lateral sclerosis (ALS) in a Chinese population. Methods In this study, 143 sporadic ALS (sALS) patients (83 men, 60 women) and 210 age- and sex-matched healthy subjects were enrolled. Blood samples were collected by venipuncture. Genomic DNA was isolated by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) according to the manufacturer’s instructions. The potential associations between ALS and GSTA1, GSTO2, and GSTZ1 polymorphisms were estimated using chi-squared analysis and unconditional logistic regression. Results The D allele and genotype frequencies of GSTO2 were increased in sALS patients compared with healthy subjects, indicating that the GSTO2 DD genotype was associated with an increased risk of sALS (odds ratio [OR] = 3.294, 95% confidence interval [CI] = 1.039–10.448). However, a significant association between the DD genotype and the risk of sALS was evident in men only (OR = 7.167, 95% CI = 1.381–37.202). Conclusion This study revealed that the D allele and genotype frequencies of GSTO2 were increased in sALS patients. The GSTO2 DD genotype was associated with an increased risk of sALS in men in a Chinese population.

scholarly journals Zinc transporters ZnT3 and ZnT6 are downregulated in the spinal cords of patients with sporadic amyotrophic lateral sclerosis

2014 ◽  
Vol 93 (2) ◽  
pp. 370-379 ◽  
Author(s):  
Masayuki Kaneko ◽  
Takao Noguchi ◽  
Saori Ikegami ◽  
Takeyuki Sakurai ◽  
Akiyoshi Kakita ◽  
...  
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Zinc Transporters ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Lateral Sclerosis

scholarly journals Patterns of Weakness, Classification of Motor Neuron Disease, and Clinical Diagnosis of Sporadic Amyotrophic Lateral Sclerosis

2015 ◽  
Vol 33 (4) ◽  
pp. 735-748 ◽  
Author(s):  
Jeffrey M. Statland ◽  
Richard J. Barohn ◽  
April L. McVey ◽  
Jonathan S. Katz ◽  
Mazen M. Dimachkie
Keyword(s):  
Amyotrophic Lateral Sclerosis ◽  
Motor Neuron ◽  
Motor Neuron Disease ◽  
Clinical Diagnosis ◽  
Sporadic Amyotrophic Lateral Sclerosis ◽  
Lateral Sclerosis
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