(Q32078766)

6 July 2017

title

Electrophysiologic endpoint measures in a multicenter ALS drug trial (English)

1 reference

multicenter clinical trial

6 July 2017

main subject

0 references

amyotrophic lateral sclerosis

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Bromberg MB

1

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6 July 2017

Fries TJ

series ordinal

2

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6 July 2017

Forshew DA

series ordinal

3

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6 July 2017

Tandan R

series ordinal

4

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6 July 2017

publication date

1 February 2001

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Journal of the Neurological Sciences

6 July 2017

published in

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6 July 2017

volume

184

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6 July 2017

issue

1

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6 July 2017

page(s)

51-55

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Electrodiagnostic studies in clinical trials for motor neuron disease

6 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group

7 January 2021

1 reference

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Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

A controlled trial of amino acid therapy in amyotrophic lateral sclerosis: I. Clinical, functional, and maximum isometric torque data

7 January 2021

1 reference

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El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

Methods for estimating numbers of motor units in biceps-brachialis muscles and losses of motor units with aging.

7 January 2021

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Macro EMG, a new recording technique

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

Motor unit fibre density in the extensor digitorum communis muscle. Single fibre electromyographic study in normal subjects at different ages

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

Motor unit number estimation, isometric strength, and electromyographic measures in amyotrophic lateral sclerosis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2800%2900489-5

Motor unit estimation: reproducibility of the spike-triggered averaging technique in normal and ALS subjects

7 January 2021

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The natural history of amyotrophic lateral sclerosis and the use of natural history controls in therapeutic trials.

7 January 2021

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Functional compensation in partially denervated muscles

7 January 2021

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Use of composite scores (megascores) to measure deficit in amyotrophic lateral sclerosis

7 January 2021

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The administration of guanidine in amyotrophic lateral sclerosis

7 January 2021

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A rating scale for amyotrophic lateral sclerosis: description and preliminary experience

7 January 2021

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A review of techniques employed to estimate the number of motor units in a muscle

7 January 2021

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Invited review: motor unit estimation: methods, results, and present status

7 January 2021

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Quantitative motor assessment in amyotrophic lateral sclerosis

7 January 2021

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Sources of error in the spike-triggered averaging method of motor unit number estimation (MUNE)

7 January 2021

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The influence of active electrode placement on CMAP amplitude

7 January 2021

1 reference

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Influence of recording site on CMAP amplitude on its variation over a length of nerve

7 January 2021

1 reference

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CMAP amplitude cartography of muscles innervated by the median, ulnar, peroneal, and tibial nerves

7 January 2021

1 reference

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A longitudinal study comparing thenar motor unit number estimates to other quantitative tests in patients with amyotrophic lateral sclerosis

7 January 2021

1 reference

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Longitudinal study of fiber density and motor unit number estimate in patients with amyotrophic lateral sclerosis

7 January 2021

1 reference

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10.1016/S0022-510X(00)00489-5

7 January 2021

Identifiers

DOI

1 reference

6 July 2017

1 reference