Literature DB >> 3714055

Quantitative motor assessment in amyotrophic lateral sclerosis.

P L Andres, W Hedlund, L Finison, T Conlon, M Felmus, T L Munsat.   

Abstract

Reliable measurements are needed to document the natural history of ALS and to determine therapeutic efficacy. We have devised a standardized protocol that generates interval data sensitive to change-the Tufts Quantitative Neuromuscular Exam (TQNE). The TQNE consists of the following four major categories: pulmonary function, oropharyngeal function, timed functional activities, and isometric strength using an electronic strain gauge. The 29-item exam takes about 1 hour to administer and has excellent test-retest reliability.

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Year:  1986        PMID: 3714055     DOI: 10.1212/wnl.36.7.937

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


  20 in total

1.  Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplex.

Authors:  Gregory Nemunaitis; Chris M Jay; Phillip B Maples; William A Gahl; Marjan Huizing; Tal Yardeni; Alex W Tong; Anagha P Phadke; Beena O Pappen; Cynthia Bedell; Henry Allen; Cathy Hernandez; Nancy S Templeton; Joseph Kuhn; Neil Senzer; John Nemunaitis
Journal:  Hum Gene Ther       Date:  2011-04-25       Impact factor: 5.695

2.  Hand-held myometry: reference values.

Authors:  R J van der Ploeg; V Fidler; H J Oosterhuis
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-03       Impact factor: 10.154

3.  Patient reported outcomes in GNE myopathy: incorporating a valid assessment of physical function in a rare disease.

Authors:  Christina Slota; Margaret Bevans; Li Yang; Joseph Shrader; Galen Joe; Nuria Carrillo
Journal:  Disabil Rehabil       Date:  2017-02-07       Impact factor: 3.033

Review 4.  Measures and markers in amyotrophic lateral sclerosis.

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

5.  Electrical impedance myography in the evaluation of the tongue musculature in amyotrophic lateral sclerosis.

Authors:  Sanjana Shellikeri; Yana Yunusova; Jordan R Green; Gary L Pattee; James D Berry; Seward B Rutkove; Lorne Zinman
Journal:  Muscle Nerve       Date:  2015-06-03       Impact factor: 3.217

Review 6.  Clinical Measures of Disease Progression in Amyotrophic Lateral Sclerosis.

Authors:  Seward B Rutkove
Journal:  Neurotherapeutics       Date:  2015-04       Impact factor: 7.620

Review 7.  Strength Testing in Motor Neuron Diseases.

Authors:  Jeremy M Shefner
Journal:  Neurotherapeutics       Date:  2017-01       Impact factor: 7.620

8.  Accuracy, reproducibility, and variability of hand-held dynamometry in motor neuron disease.

Authors:  A Goonetilleke; H Modarres-Sadeghi; R J Guiloff
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-03       Impact factor: 10.154

9.  Laboratory testing of muscle function in the management of neuromuscular disease.

Authors:  C M Wiles; Y Karni; J Nicklin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-05       Impact factor: 10.154

10.  Inclusion body myositis: clinical and histopathological features of 36 patients.

Authors:  S Beyenburg; S Zierz; F Jerusalem
Journal:  Clin Investig       Date:  1993-05
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