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 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
  5. 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
  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. doi request reprint A single blind randomized controlled clinical trial of mexiletine in amyotrophic lateral sclerosis: Efficacy and safety of sodium channel blocker phase II trial
    Kazumoto Shibuya
    a Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Amyotroph Lateral Scler Frontotemporal Degener 16:353-8. 2015

Collaborators

  • Sonoko Misawa
  • Satoshi Kuwabara
  • Toshiki Mizuno
  • Kensuke Shiga
  • Toshio Shimizu
  • Masahiro Mori
  • Yasumasa Yoshiyama
  • Nobuhiro Yuki
  • Chihiro Fujii
  • Setsu Sawai
  • Kazumoto Shibuya
  • Yumi Fujimaki
  • Yukari Sekiguchi
  • Masanori Nakagawa
  • Kazuaki Kanai
  • Saiko Nasu
  • Hisashi Takahashi
  • Yasunori Sato
  • Shigeki Ohmori
  • Sagiri Isose
  • Soichiro Numa
  • Akihiro Tanaka
  • Tomoyuki Ohara
  • Takashi Kasai
  • Naoki Tokuda
  • Ayaka Kimura
  • Yukie Kushimura
  • Ryotaro Ishii
  • Takayuki Kondo
  • Shunya Nakane
  • Kanako Morita
  • Naoki Makita
  • Yukie Kushimura-Okada
  • Osamu Higuchi
  • Hideki Kimura
  • Yukiko Tsuji
  • Satsuki Mitsuma
  • Keisuke Watanabe
  • Kyoko Sawaguchi
  • Yuta Iwai
  • Fumitoshi Niwa
  • Hideki Hanaoka
  • Fukiko Kitani-Morii
  • Ai Hamano
  • Minako Beppu
  • Ikuko Mizuta
  • Shiro Matsubara
  • Francesca Notturno
  • Antonino Uncini
  • Cindy S Y Lin
  • Yumiko Kugio
  • Takuro Horikoshi
  • Kimiko Ito
  • Chiaki Nakaseko
  • Hiroshi Kitamura
  • Miho Nakata
  • Kimihito Arai

Detail Information

Publications16

  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 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
    ....
  5. 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...
  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. doi request reprint A single blind randomized controlled clinical trial of mexiletine in amyotrophic lateral sclerosis: Efficacy and safety of sodium channel blocker phase II trial
    Kazumoto Shibuya
    a Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan
    Amyotroph Lateral Scler Frontotemporal Degener 16:353-8. 2015
    ..We have to attempt another trial using a higher dose of mexiletine or other agents to suppress sodium currents and ALS progression in the future. ..
  11. pmc Myasthenic symptoms in anti-low-density lipoprotein receptor-related protein 4 antibody-seropositive amyotrophic lateral sclerosis: two case reports
    Hisashi Takahashi
    Department of Neurology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, 465 Kajii cho, Kamigyo ku, Kyoto, 602 0841, Japan
    BMC Neurol 16:229. 2016
    ..Recent studies suggested that antibody to low-density lipoprotein receptor-related protein 4 (LRP4) was a pathogenic agent of myasthenia gravis (MG), and it was also detected in ALS patients...
  12. doi request reprint Parasympathetic Dominant Autonomic Dysfunction in Charcot-Marie-Tooth Disease Type 2J with the MPZ Thr124Met Mutation
    Naoki Tokuda
    Department of Neurology, Kyoto Prefectural University of Medicine, Graduate School of Medicine, Japan
    Intern Med 54:1919-22. 2015
    ..Our case suggests that mainly the parasympathetic autonomic function is disturbed in CMT2J. ..
  13. doi request reprint Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease
    Yu Ichi Noto
    Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan
    J Neurol Neurosurg Psychiatry 86:378-84. 2015
    ....
  14. doi 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...
  15. 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...
  16. doi request reprint An Adult Case of Anti-Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-associated Multiphasic Acute Disseminated Encephalomyelitis at 33-year Intervals
    Soichiro Numa
    Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Japan
    Intern Med 55:699-702. 2016
    ..This phenotype has only previously been reported in pediatric cases. Neurologists thus need to be aware that the phenotype may occur in adult patients, in whom it may be assumed to be atypical multiple sclerosis...