Literature DB >> 9710047

A loss of functional spinal alpha motor neurons in amyotrophic lateral sclerosis.

K Arasaki1, M Tamaki.   

Abstract

We obtained motor unit number estimates (MUNEs) of the hypothenar and the extensor digitorum brevis muscles in ALS patients by our new technique. One year after symptom onset, the MUNEs had decreased to +/-30% of normal. Accordingly, we suggest that 70% of functional spinal alpha motor neurons are lost in the first post-onset year in ALS.

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Year:  1998        PMID: 9710047     DOI: 10.1212/wnl.51.2.603

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

Review 1.  Measures and markers in amyotrophic lateral sclerosis.

Authors:  Merit Cudkowicz; Muhammad Qureshi; Jeremy Shefner
Journal:  NeuroRx       Date:  2004-04

2.  Chronic exposure to dietary sterol glucosides is neurotoxic to motor neurons and induces an ALS-PDC phenotype.

Authors:  R C Tabata; J M B Wilson; P Ly; P Zwiegers; D Kwok; J M Van Kampen; N Cashman; C A Shaw
Journal:  Neuromolecular Med       Date:  2008-01-15       Impact factor: 3.843

3.  Treatment of progressive paralysis associated with cervical myelopathy and suspected amyotrophic lateral sclerosis: A case report.

Authors:  Yoshinori Ishikawa; Naohisa Miyakoshi; Takashi Kobayashi; Toshihiko Kikuchi
Journal:  Surg Neurol Int       Date:  2021-11-02
  3 in total

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