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Items: 1 to 20 of 120

1.
2.

Functional over-load saves motor units in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis.

Gordon T, Tyreman N, Li S, Putman CT, Hegedus J.

Neurobiol Dis. 2010 Feb;37(2):412-22. doi: 10.1016/j.nbd.2009.10.021. Epub 2009 Oct 29.

PMID:
19879358
3.

Motor unit number estimation in evaluating disease progression in patients with amyotrophic lateral sclerosis.

Ahn SW, Kim SH, Oh DH, Kim SM, Park KS, Hong YH, Kwon OS, Sung JJ, Lee KW.

J Korean Med Sci. 2010 Sep;25(9):1359-63. doi: 10.3346/jkms.2010.25.9.1359. Epub 2010 Aug 14.

4.

Motor unit number estimates correlate with strength in polio survivors.

Sorenson EJ, Daube JR, Windebank AJ.

Muscle Nerve. 2006 Nov;34(5):608-13.

PMID:
16929544
5.

Comparison of incremental with multipoint MUNE methods in transgenic ALS mice.

Shefner JM, Cudkowicz ME, Brown RH Jr.

Muscle Nerve. 2002 Jan;25(1):39-42.

PMID:
11754183
6.

Progressive motor unit loss in the G93A mouse model of amyotrophic lateral sclerosis is unaffected by gender.

Hegedus J, Putman CT, Gordon T.

Muscle Nerve. 2009 Mar;39(3):318-27. doi: 10.1002/mus.21160.

PMID:
19208415
7.
8.

Time course of preferential motor unit loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis.

Hegedus J, Putman CT, Gordon T.

Neurobiol Dis. 2007 Nov;28(2):154-64. Epub 2007 Jul 10.

PMID:
17766128
9.
11.

Pre-symptomatic detection of chronic motor deficits and genotype prediction in congenic B6.SOD1(G93A) ALS mouse model.

Hayworth CR, Gonzalez-Lima F.

Neuroscience. 2009 Dec 15;164(3):975-85. doi: 10.1016/j.neuroscience.2009.08.031. Epub 2009 Aug 20.

12.

The relationship between Bayesian motor unit number estimation and histological measurements of motor neurons in wild-type and SOD1(G93A) mice.

Ngo ST, Baumann F, Ridall PG, Pettitt AN, Henderson RD, Bellingham MC, McCombe PA.

Clin Neurophysiol. 2012 Oct;123(10):2080-91. doi: 10.1016/j.clinph.2012.01.028. Epub 2012 Apr 20.

PMID:
22521362
13.

Stratifying disease stages with different progression rates determined by electrophysiological tests in patients with amyotrophic lateral sclerosis.

Liu XX, Zhang J, Zheng JY, Zhang S, Xu YS, Kang DX, Fan DS.

Muscle Nerve. 2009 Mar;39(3):304-9. doi: 10.1002/mus.21144.

PMID:
19208412
14.

Development and use of the incremental twitch subtraction MUNE method in mice.

Hegedus J, Jones KE, Gordon T.

Suppl Clin Neurophysiol. 2009;60:209-17.

PMID:
20715384
15.

Motor unit number index (MUNIX) versus motor unit number estimation (MUNE): a direct comparison in a longitudinal study of ALS patients.

Boekestein WA, Schelhaas HJ, van Putten MJ, Stegeman DF, Zwarts MJ, van Dijk JP.

Clin Neurophysiol. 2012 Aug;123(8):1644-9. doi: 10.1016/j.clinph.2012.01.004. Epub 2012 Feb 8.

PMID:
22321299
16.

A method comparison in monitoring disease progression of G93A mouse model of ALS.

Zhou C, Zhao CP, Zhang C, Wu GY, Xiong F, Zhang C.

Amyotroph Lateral Scler. 2007 Dec;8(6):366-72. Epub 2007 Jul 31.

PMID:
17852023
17.

[Progression rate of MUNE at diagnosis: a prognostic factor of survival in patients with amyotrophic lateral sclerosis].

Liu XX, Fan DS, Zhang J, Zheng JY, Zhang S.

Beijing Da Xue Xue Bao Yi Xue Ban. 2008 Dec 18;40(6):629-32. Chinese.

18.

Intra-rater reliability of motor unit number estimation and quantitative motor unit analysis in subjects with amyotrophic lateral sclerosis.

Ives CT, Doherty TJ.

Clin Neurophysiol. 2014 Jan;125(1):170-8. doi: 10.1016/j.clinph.2013.04.345. Epub 2013 Jul 16.

PMID:
23867065
19.

Effect of neurophilin ligands on motor units in mice with SOD1 ALS mutations.

Shefner JM, Brown RH Jr, Cole D, Chaturvedi P, Schoenfeld D, Pastuszak K, Matthews R, Upton-Rice M, Cudkowicz ME.

Neurology. 2001 Nov 27;57(10):1857-61.

PMID:
11723276
20.

Method for counting motor units in mice and validation using a mathematical model.

Major LA, Hegedus J, Weber DJ, Gordon T, Jones KE.

J Neurophysiol. 2007 Feb;97(2):1846-56. Epub 2006 Dec 6.

PMID:
17151224

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