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Open AccessJournal ArticleDOI

New hope for patients with pure lower motor neuron syndromes.

J.H.J. Wokke, +1 more
- 01 Jul 1999 - 
- Vol. 67, Iss: 1, pp 6-6
TLDR
For patients with probable or definite motor neuron disease according to established criteria, the recent introduction of the antiglutamate drug riluzole gives a mean prolongation of life after diagnosis of some 3 months.
Abstract
Motor neuron disease is still one of the most dramatic neurological conditions; it reflects a range of which one end encompasses patients with the bulbar form of amyotrophic lateral sclerosis who have dysarthria and dysphagia and have a dramatically shortened life expectancy. For patients with probable or definite motor neuron disease according to established criteria, the recent introduction of the antiglutamate drug riluzole gives a mean prolongation of life after diagnosis of some 3 months.1 The other end of the range of motor neuron disease is formed by patients with so called multifocal motor neuropathy. This is characterised by lower motor neuron dysfunction in the areas of selected motor nerves. Neurophysiological demonstration of conduction block over these nerves is pivotal for the diagnosis.2 Before the discovery of multifocal motor neuropathy as a separate and treatable condition, patients with …

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Citations
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Journal ArticleDOI

New hope for patients with pure lower motor neurons syndromes.

TL;DR: It is recommended to recommend referral for all patients with motor neuron disease, especially in cases in the initial stages or in atypical forms, in which the diagnosis …
References
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Journal ArticleDOI

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis

TL;DR: The antiglutamate agent riluzole appears to slow the progression of amyotrophic lateral sclerosis, and it may improve survival in patients with disease of bulbar onset, according to a prospective, double-blind, placebo-controlled trial in 155 outpatients with Amyotrophicateral sclerosis.
Journal ArticleDOI

Multifocal acquired demyelinating neuropathy masqurading as motor neuron disease

TL;DR: Five patients with pure motor neuropathy characterized by multifocal weakness, muscle atrophy that was sometimes profound, cramps, and fasciculations with relatively preserved reflexes are reported, with distinction from motor neuron disease critical.
Journal ArticleDOI

Multifocal motor neuropathy with conduction block: Is it a distinct clinical entity?

TL;DR: The clinical syndrome associated with multifocal conduction block seemed uniform, however, and patients with conductionBlock had slower progression if there were no upper motor neuron signs.
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