Yu Ichi Noto

Summary

Affiliation: Kyoto Prefectural University of Medicine
Country: Japan

Publications

  1. doi request reprint Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: evidence of activity-dependent conduction block
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 124:1893-8. 2013
  2. doi request reprint Awaji ALS criteria increase the diagnostic sensitivity in patients with bulbar onset
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 123:382-5. 2012
  3. doi request reprint Elevated CSF TDP-43 levels in amyotrophic lateral sclerosis: specificity, sensitivity, and a possible prognostic value
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Japan
    Amyotroph Lateral Scler 12:140-3. 2011
  4. doi request reprint Distal motor axonal dysfunction in amyotrophic lateral sclerosis
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    J Neurol Sci 302:58-62. 2011
  5. doi request reprint Activity-dependent changes in impulse conduction of single human motor axons: a stimulated single fiber electromyography study
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 122:2512-7. 2011
  6. doi request reprint Differences in excitability between median and superficial radial sensory axons
    Yumi Fujimaki
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 123:1440-5. 2012
  7. doi request reprint Antiganglioside antibodies are associated with axonal Guillain-Barré syndrome: a Japanese-Italian collaborative study
    Yukari Sekiguchi
    Department of Neurology, Graduate School of Medicine, Chiba University, 1 8 1 Inohana, Chuo Ku, Chiba 260 8670, Japan
    J Neurol Neurosurg Psychiatry 83:23-8. 2012
  8. doi request reprint Markedly reduced axonal potassium channel expression in human sporadic amyotrophic lateral sclerosis: an immunohistochemical study
    Kazumoto Shibuya
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Exp Neurol 232:149-53. 2011
  9. ncbi request reprint Detection of bone lesions by CT in POEMS syndrome
    Kazumoto Shibuya
    Department of Neurology, Graduate School of Medicine, Chiba University, Japan
    Intern Med 50:1393-6. 2011
  10. ncbi request reprint Contrasting echogenicity in flexor digitorum profundus-flexor carpi ulnaris: a diagnostic ultrasound pattern in sporadic inclusion body myositis
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465 Kajii cho, Kamigyo ku, Kyoto, 602 0841, Japan
    Muscle Nerve 49:745-8. 2014

Collaborators

Detail Information

Publications11

  1. doi request reprint Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: evidence of activity-dependent conduction block
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 124:1893-8. 2013
    ....
  2. doi request reprint Awaji ALS criteria increase the diagnostic sensitivity in patients with bulbar onset
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 123:382-5. 2012
    ..In Awaji ALS criteria, fasciculation potentials are regarded as evidence of acute denervation in the presence of chronic neurogenic changes on needle electromyography...
  3. doi request reprint Elevated CSF TDP-43 levels in amyotrophic lateral sclerosis: specificity, sensitivity, and a possible prognostic value
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Japan
    Amyotroph Lateral Scler 12:140-3. 2011
    ..Moreover, among ALS patients, lower levels of CSF TDP-43 may reflect the accumulation of TDP-43 in the cortical and spinal motor neurons and thereby shorter survival time, although this should be confirmed in larger prospective studies...
  4. doi request reprint Distal motor axonal dysfunction in amyotrophic lateral sclerosis
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    J Neurol Sci 302:58-62. 2011
    ..We suggest that recognition of the pattern of distal motor axonal dysfunction predominant in the median nerve is clinically important, and could provide additional insights into the pathophysiology of ALS...
  5. doi request reprint Activity-dependent changes in impulse conduction of single human motor axons: a stimulated single fiber electromyography study
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 122:2512-7. 2011
    ....
  6. doi request reprint Differences in excitability between median and superficial radial sensory axons
    Yumi Fujimaki
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Clin Neurophysiol 123:1440-5. 2012
    ..g., axons innervating the glabrous and hairy skin in the hand). Previous studies have shown that excitability properties differ between motor and sensory axons, and even among sensory axons between median and sural sensory axons...
  7. doi request reprint Antiganglioside antibodies are associated with axonal Guillain-Barré syndrome: a Japanese-Italian collaborative study
    Yukari Sekiguchi
    Department of Neurology, Graduate School of Medicine, Chiba University, 1 8 1 Inohana, Chuo Ku, Chiba 260 8670, Japan
    J Neurol Neurosurg Psychiatry 83:23-8. 2012
    ..Whether or not antiganglioside antibodies are related to axonal or demyelinating Guillain-Barré syndrome (GBS) is still a matter of controversy, as detailed in previous studies conducted in Western and Asian countries...
  8. doi request reprint Markedly reduced axonal potassium channel expression in human sporadic amyotrophic lateral sclerosis: an immunohistochemical study
    Kazumoto Shibuya
    Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Exp Neurol 232:149-53. 2011
    ..The axonal hyperexcitability would lead to generation of fasciculations, and possibly enhances motor neuron death in ALS...
  9. ncbi request reprint Detection of bone lesions by CT in POEMS syndrome
    Kazumoto Shibuya
    Department of Neurology, Graduate School of Medicine, Chiba University, Japan
    Intern Med 50:1393-6. 2011
    ..Therefore it is important to correctly identify the number of bone lesions...
  10. ncbi request reprint Contrasting echogenicity in flexor digitorum profundus-flexor carpi ulnaris: a diagnostic ultrasound pattern in sporadic inclusion body myositis
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465 Kajii cho, Kamigyo ku, Kyoto, 602 0841, Japan
    Muscle Nerve 49:745-8. 2014
    ..In this study we aimed to clarify whether muscle ultrasound (US) of the forearm can be used to differentiate between patients with sporadic inclusion body myositis (s-IBM) and those with s-IBM-mimicking diseases...
  11. ncbi request reprint Demyelinating features in sensory nerve conduction in Fisher syndrome
    Kensuke Shiga
    Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Japan
    Intern Med 51:2307-12. 2012
    ..Previous studies have shown the amplitudes of sensory nerve action potentials (SNAPs) to decrease in patients with FS, thus implying the presence of an axonal pathology in the sensory nerves...