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Journal Abstract Search

401 related items for PubMed ID: 16036422

  • 1. Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials.
    de Carvalho M, Chio A, Dengler R, Hecht M, Weber M, Swash M.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Mar; 6(1):17-28. PubMed ID: 16036422
    [Abstract] [Full Text] [Related]

  • 2. The Neurophysiological Index in ALS.
    Swash M, de Carvalho M.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2004 Sep; 5 Suppl 1():108-10. PubMed ID: 15512888
    [Abstract] [Full Text] [Related]

  • 3. Clinical neurophysiology in ALS.
    Inghilleri M, Iacovelli E.
    Arch Ital Biol; 2011 Mar; 149(1):57-63. PubMed ID: 21412716
    [Abstract] [Full Text] [Related]

  • 4. [Objective markers for upper motor neuron involvement in amyotrophic lateral sclerosis].
    Iwata NK.
    Brain Nerve; 2007 Oct; 59(10):1053-64. PubMed ID: 17969345
    [Abstract] [Full Text] [Related]

  • 5. Sensitivity of electrophysiological tests for upper and lower motor neuron dysfunction in ALS: a six-month longitudinal study.
    de Carvalho M, Swash M.
    Muscle Nerve; 2010 Feb; 41(2):208-11. PubMed ID: 19697379
    [Abstract] [Full Text] [Related]

  • 6. The natural history of central motor abnormalities in amyotrophic lateral sclerosis.
    Mills KR.
    Brain; 2003 Nov; 126(Pt 11):2558-66. PubMed ID: 12937082
    [Abstract] [Full Text] [Related]

  • 7. Motor unit number estimation, isometric strength, and electromyographic measures in amyotrophic lateral sclerosis.
    Bromberg MB, Forshew DA, Nau KL, Bromberg J, Simmons Z, Fries TJ.
    Muscle Nerve; 1993 Nov; 16(11):1213-9. PubMed ID: 8413373
    [Abstract] [Full Text] [Related]

  • 8. Magnetic stimulation including the triple-stimulation technique in amyotrophic lateral sclerosis.
    Attarian S, Verschueren A, Pouget J.
    Muscle Nerve; 2007 Jul; 36(1):55-61. PubMed ID: 17443663
    [Abstract] [Full Text] [Related]

  • 9. 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. PubMed ID: 19208412
    [Abstract] [Full Text] [Related]

  • 10. Motor unit number estimates and quantitative motor unit analysis in healthy subjects and patients with amyotrophic lateral sclerosis.
    Boe SG, Stashuk DW, Doherty TJ.
    Muscle Nerve; 2007 Jul; 36(1):62-70. PubMed ID: 17455264
    [Abstract] [Full Text] [Related]

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  • 12. Progression of cortical and spinal dysfunctions over time in amyotrophic lateral sclerosis.
    Attarian S, Vedel JP, Pouget J, Schmied A.
    Muscle Nerve; 2008 Mar; 37(3):364-75. PubMed ID: 18080998
    [Abstract] [Full Text] [Related]

  • 13. Clinical trials in ALS: a review of the role of clinical and neurophysiological measurements.
    de Carvalho M, Costa J, Swash M.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec; 6(4):202-12. PubMed ID: 16319023
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  • 16. Clinical utility of trapezius muscle studies in the evaluation of amyotrophic lateral sclerosis.
    Cho JY, Sung JJ, Min JH, Lee KW.
    J Clin Neurosci; 2006 Nov; 13(9):908-12. PubMed ID: 17049243
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  • 18. Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.
    Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP.
    Neurology; 2009 Jun 02; 72(22):1948-52. PubMed ID: 19487653
    [Abstract] [Full Text] [Related]

  • 19. Sources of error in the spike-triggered averaging method of motor unit number estimation (MUNE).
    Bromberg MB, Abrams JL.
    Muscle Nerve; 1995 Oct 02; 18(10):1139-46. PubMed ID: 7659108
    [Abstract] [Full Text] [Related]

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