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249 related items for PubMed ID: 16892429

  • 21. 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. PubMed ID: 23867065
    [Abstract] [Full Text] [Related]

  • 22. Development and use of the incremental twitch subtraction MUNE method in mice.
    Hegedus J, Jones KE, Gordon T.
    Suppl Clin Neurophysiol; 2009 Jan; 60():209-17. PubMed ID: 20715384
    [Abstract] [Full Text] [Related]

  • 23. Statistical MUNE: a comparison of two methods of setting recording windows in healthy subjects and ALS patients.
    Hong YH, Sung JJ, Park KS, Kwon O, Min JH, Lee KW.
    Clin Neurophysiol; 2007 Dec; 118(12):2605-11. PubMed ID: 17911043
    [Abstract] [Full Text] [Related]

  • 24. Sources of error in the spike-triggered averaging method of motor unit number estimation (MUNE).
    Bromberg MB, Abrams JL.
    Muscle Nerve; 1995 Oct; 18(10):1139-46. PubMed ID: 7659108
    [Abstract] [Full Text] [Related]

  • 25. MUNIX and incremental stimulation MUNE in ALS patients and control subjects.
    Furtula J, Johnsen B, Christensen PB, Pugdahl K, Bisgaard C, Christensen MK, Arentsen J, Frydenberg M, Fuglsang-Frederiksen A.
    Clin Neurophysiol; 2013 Mar; 124(3):610-8. PubMed ID: 23040293
    [Abstract] [Full Text] [Related]

  • 26. Motor unit number estimation as a complementary test to routine electromyography in the diagnosis of amyotrophic lateral sclerosis.
    Gawel M, Zalewska E, Lipowska M, Kostera-Pruszczyk A, Szmidt-Salkowska E, Kaminska A.
    J Electromyogr Kinesiol; 2016 Feb; 26():60-5. PubMed ID: 26614440
    [Abstract] [Full Text] [Related]

  • 27. Effect of neurophilin ligands on motor units in mice with SOD1 ALS mutations.
    Shefner JM, Brown RH, Cole D, Chaturvedi P, Schoenfeld D, Pastuszak K, Matthews R, Upton-Rice M, Cudkowicz ME.
    Neurology; 2001 Nov 27; 57(10):1857-61. PubMed ID: 11723276
    [Abstract] [Full Text] [Related]

  • 28. Asymmetry of motor unit number estimate and its rate of decline in patients with amyotrophic lateral sclerosis.
    Ahn SW, Kim JE, Sung JJ, Lee KW, Hong YH.
    J Clin Neurophysiol; 2011 Oct 27; 28(5):528-32. PubMed ID: 21946374
    [Abstract] [Full Text] [Related]

  • 29. [Comparison of multiple point stimulation and incremental stimulation in patients with amyotrophic lateral sclerosis].
    Xu YS, Zheng JY, Zhang S, Song HS, Zhang J, Fan DS.
    Zhonghua Yi Xue Za Zhi; 2009 Nov 24; 89(43):3051-4. PubMed ID: 20137632
    [Abstract] [Full Text] [Related]

  • 30. 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. PubMed ID: 19699279
    [Abstract] [Full Text] [Related]

  • 31. ALS surrogate markers. MUNE.
    Gooch CL, Shefner JM.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2004 Sep 15; 5 Suppl 1():104-7. PubMed ID: 15512887
    [Abstract] [Full Text] [Related]

  • 32. Longitudinal study of fiber density and motor unit number estimate in patients with amyotrophic lateral sclerosis.
    Yuen EC, Olney RK.
    Neurology; 1997 Aug 15; 49(2):573-8. PubMed ID: 9270599
    [Abstract] [Full Text] [Related]

  • 33. Cholinergic modulation of motor neurons through the C-boutons are necessary for the locomotor compensation for severe motor neuron loss during amyotrophic lateral sclerosis disease progression.
    Landoni LM, Myles JR, Wells TL, Mayer WP, Akay T.
    Behav Brain Res; 2019 Sep 02; 369():111914. PubMed ID: 31022419
    [Abstract] [Full Text] [Related]

  • 34. Presymptomatic electrophysiological tests predict clinical onset and survival in SOD1(G93A) ALS mice.
    Mancuso R, Osta R, Navarro X.
    Muscle Nerve; 2014 Dec 02; 50(6):943-9. PubMed ID: 24619579
    [Abstract] [Full Text] [Related]

  • 35. Statistical motor unit number estimation and ALS trials: the effect of motor unit instability.
    Shefner JM.
    Suppl Clin Neurophysiol; 2009 Dec 02; 60():135-41. PubMed ID: 20715375
    [Abstract] [Full Text] [Related]

  • 36. Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression.
    Bruneteau G, Simonet T, Bauché S, Mandjee N, Malfatti E, Girard E, Tanguy ML, Behin A, Khiami F, Sariali E, Hell-Remy C, Salachas F, Pradat PF, Fournier E, Lacomblez L, Koenig J, Romero NB, Fontaine B, Meininger V, Schaeffer L, Hantaï D.
    Brain; 2013 Aug 02; 136(Pt 8):2359-68. PubMed ID: 23824486
    [Abstract] [Full Text] [Related]

  • 37. Quantitating progression in ALS.
    de Carvalho M, Scotto M, Lopes A, Swash M.
    Neurology; 2005 May 24; 64(10):1783-5. PubMed ID: 15911812
    [Abstract] [Full Text] [Related]

  • 38. Motor neuron dysfunction in a mouse model of ALS: gender-dependent effect of P2X7 antagonism.
    Cervetto C, Frattaroli D, Maura G, Marcoli M.
    Toxicology; 2013 Sep 06; 311(1-2):69-77. PubMed ID: 23583883
    [Abstract] [Full Text] [Related]

  • 39. Motor unit number estimate-based rates of progression of ALS predict patient survival.
    Armon C, Brandstater ME.
    Muscle Nerve; 1999 Nov 06; 22(11):1571-5. PubMed ID: 10514236
    [Abstract] [Full Text] [Related]

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