| Year |
Citation |
Score |
| 2023 |
Takahashi M, Shimokawa T, Koh J, Takeshima T, Yamashita H, Kajimoto Y, Ito H. Effect of istradefylline on postural abnormalities in patients with Parkinson's disease: An association study of baseline postural angle measurements with changes in Unified Dystonia Rating Scale total score. Eneurologicalsci. 34: 100493. PMID 38274039 DOI: 10.1016/j.ensci.2023.100493 |
0.644 |
|
| 2022 |
Takahashi M, Shimokawa T, Koh J, Takeshima T, Yamashita H, Kajimoto Y, Mori A, Ito H. Efficacy and safety of istradefylline in patients with Parkinson's disease presenting with postural abnormalities: Results from a multicenter, prospective, and open-label exploratory study in Japan. Journal of the Neurological Sciences. 432: 120078. PMID 34923334 DOI: 10.1016/j.jns.2021.120078 |
0.652 |
|
| 2020 |
Hayashida A, Li Y, Yoshino H, Daida K, Ikeda A, Ogaki K, Fuse A, Mori A, Takanashi M, Nakahara T, Yoritaka A, Tomizawa Y, Furukawa Y, Kanai K, Nakayama Y, ... Ito H, et al. The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1. Neurobiology of Aging. PMID 32713623 DOI: 10.1016/J.Neurobiolaging.2020.06.017 |
0.527 |
|
| 2020 |
Kawamoto Y, Ayaki T, Urushitani M, Ito H, Takahashi R. Accumulation of HAX-1 and PARL in brainstem- and cortical-type Lewy bodies in Parkinson's disease and dementia with Lewy bodies. Journal of the Neurological Sciences. 415: 116928. PMID 32470650 DOI: 10.1016/J.Jns.2020.116928 |
0.343 |
|
| 2019 |
Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata KY, Mori M, Inamori Y, Matsui N, Kimura E, Kusaka H, Kondo T, Ito H, Higuchi I, Hashiguchi A, Nodera H, et al. The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan. Orphanet Journal of Rare Diseases. 14: 155. PMID 31242950 DOI: 10.1186/S13023-019-1122-5 |
0.534 |
|
| 2019 |
Yamaguchi Y, Ayaki T, Li F, Tsujimura A, Kamada M, Ito H, Maki T, Sawamoto N, Urushitani M, Takahashi R. Phosphorylated NF-κB subunit p65 aggregates in granulovacuolar degeneration and neurites in neurodegenerative diseases with tauopathy. Neuroscience Letters. PMID 30946927 DOI: 10.1016/J.Neulet.2019.03.036 |
0.346 |
|
| 2018 |
Oki R, Izumi Y, Nodera H, Sato Y, Nokihara H, Kanai K, Sonoo M, Urushitani M, Nishinaka K, Atsuta N, Kohara N, Shimizu T, Kikuchi H, Oda M, Ikeda K, ... ... Ito H, et al. The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled Trial. Jmir Research Protocols. 7: e12046. PMID 30578206 DOI: 10.2196/12046 |
0.359 |
|
| 2017 |
Ayaki T, Ito H, Komure O, Kamada M, Nakamura M, Wate R, Kusaka H, Yamaguchi Y, Li F, Kawakami H, Urushitani M, Takahashi R. Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations. Journal of Neuropathology and Experimental Neurology. PMID 29272468 DOI: 10.1093/Jnen/Nlx109 |
0.598 |
|
| 2017 |
Honjo Y, Ayaki T, Tomiyama T, Horibe T, Ito H, Mori H, Takahashi R, Kawakami K. Decreased levels of PDI and P5 in oligodendrocytes in Alzheimer's disease. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 28731225 DOI: 10.1111/Neup.12395 |
0.311 |
|
| 2017 |
Imamura K, Izumi Y, Watanabe A, Tsukita K, Woltjen K, Yamamoto T, Hotta A, Kondo T, Kitaoka S, Ohta A, Tanaka A, Watanabe D, Morita M, Takuma H, Tamaoka A, ... ... Ito H, et al. The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis. Science Translational Medicine. 9. PMID 28539470 DOI: 10.1126/Scitranslmed.Aaf3962 |
0.528 |
|
| 2017 |
Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige SI, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y, Tsuji S. Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations. Cerebellum (London, England). PMID 28150130 DOI: 10.1007/S12311-017-0846-9 |
0.302 |
|
| 2017 |
Tsuji K, Nakayama Y, Ayaki T, Hironishi M, Ito H. Comparative immunohistochemical study on the past and the recent kii amyotrophic lateral sclerosis patients Journal of the Neurological Sciences. 381: 717. DOI: 10.1016/J.Jns.2017.08.2019 |
0.333 |
|
| 2017 |
Nakanishi I, Yamamoto Y, Ito H. Subjective evaluation of the coaching in patients with Parkinson's disease Journal of the Neurological Sciences. 381: 589. DOI: 10.1016/J.Jns.2017.08.1660 |
0.483 |
|
| 2016 |
Nakazawa S, Oikawa D, Ishii R, Ayaki T, Takahashi H, Takeda H, Ishitani R, Kamei K, Takeyoshi I, Kawakami H, Iwai K, Hatada I, Sawasaki T, Ito H, Nureki O, et al. Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis. Nature Communications. 7: 12547. PMID 27552911 DOI: 10.1038/Ncomms12547 |
0.339 |
|
| 2016 |
Murata KY, Nakatani K, Yananeki M, Nakanishi I, Ito H. Anti-U3 ribonucleoprotein antibody-positive inflammatory myopathy: a case report. Journal of Medical Case Reports. 10: 169. PMID 27283724 DOI: 10.1186/S13256-016-0941-4 |
0.467 |
|
| 2016 |
Uchida T, Tamaki Y, Ayaki T, Shodai A, Kaji S, Morimura T, Banno Y, Nishitsuji K, Sakashita N, Maki T, Yamashita H, Ito H, Takahashi R, Urushitani M. CUL2-mediated clearance of misfolded TDP-43 is paradoxically affected by VHL in oligodendrocytes in ALS. Scientific Reports. 6: 19118. PMID 26751167 DOI: 10.1038/Srep19118 |
0.59 |
|
| 2015 |
Honjo Y, Ayaki T, Tomiyama T, Horibe T, Ito H, Mori H, Takahashi R, Kawakami K. Increased GADD34 in oligodendrocytes in Alzheimer's disease. Neuroscience Letters. 602: 50-5. PMID 26142647 DOI: 10.1016/J.Neulet.2015.06.052 |
0.326 |
|
| 2015 |
Murata KY, Maeba A, Yamanegi M, Nakanishi I, Ito H. Methotrexate myelopathy after intrathecal chemotherapy: a case report. Journal of Medical Case Reports. 9: 135. PMID 26055509 DOI: 10.1186/S13256-015-0597-5 |
0.506 |
|
| 2014 |
Ayaki T, Ito H, Fukushima H, Inoue T, Kondo T, Ikemoto A, Asano T, Shodai A, Fujita T, Fukui S, Morino H, Nakano S, Kusaka H, Yamashita H, Ihara M, et al. Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant. Acta Neuropathologica Communications. 2: 172. PMID 25492614 DOI: 10.1186/S40478-014-0172-0 |
0.757 |
|
| 2014 |
Kawamoto Y, Ito H, Ayaki T, Takahashi R. Immunohistochemical localization of apoptosome-related proteins in Lewy bodies in Parkinson's disease and dementia with Lewy bodies. Brain Research. 1571: 39-48. PMID 24835407 DOI: 10.1016/J.Brainres.2014.05.007 |
0.311 |
|
| 2014 |
Ito H. Basophilic inclusions and neuronal intermediate filament inclusions in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 589-95. PMID 24673472 DOI: 10.1111/Neup.12119 |
0.341 |
|
| 2014 |
Honjo Y, Horibe T, Torisawa A, Ito H, Nakanishi A, Mori H, Komiya T, Takahashi R, Kawakami K. Protein disulfide isomerase P5-immunopositive inclusions in patients with Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 38: 601-9. PMID 24037032 DOI: 10.3233/Jad-130632 |
0.303 |
|
| 2014 |
Oono M, Okado-Matsumoto A, Shodai A, Ido A, Ohta Y, Abe K, Ayaki T, Ito H, Takahashi R, Taniguchi N, Urushitani M. Transglutaminase 2 accelerates neuroinflammation in amyotrophic lateral sclerosis through interaction with misfolded superoxide dismutase 1. Journal of Neurochemistry. 128: 403-18. PMID 24032595 DOI: 10.1111/Jnc.12441 |
0.376 |
|
| 2014 |
Kawamoto Y, Ito H, Ihara M, Takahashi R. XIAP immunoreactivity in glial and neuronal cytoplasmic inclusions in multiple system atrophy. Clinical Neuropathology. 33: 76-83. PMID 23993308 DOI: 10.5414/Np300610 |
0.333 |
|
| 2014 |
Kamada M, Izumi Y, Ayaki T, Nakamura M, Kagawa S, Kudo E, Sako W, Maruyama H, Nishida Y, Kawakami H, Ito H, Kaji R. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 64-70. PMID 23889540 DOI: 10.1111/Neup.12051 |
0.393 |
|
| 2014 |
Nakamura S, Wate R, Kaneko S, Ito H, Oki M, Tsuge A, Nagashima M, Asayama S, Fujita K, Nakamura M, Maruyama H, Kawakami H, Kusaka H. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 58-63. PMID 23773010 DOI: 10.1111/Neup.12049 |
0.611 |
|
| 2013 |
Egawa N, Kitaoka S, Tsukita K, Naitoh M, Takahashi K, Yamamoto T, Adachi F, Kondo T, Okita K, Asaka I, Aoi T, Watanabe A, Yamada Y, Morizane A, Takahashi J, ... ... Ito H, et al. Response to comment on "Drug screening for ALS using patient-specific induced pluripotent stem cells". Science Translational Medicine. 5: 188lr2. PMID 23740898 DOI: 10.1126/Scitranslmed.3005697 |
0.546 |
|
| 2013 |
Akizuki M, Yamashita H, Uemura K, Maruyama H, Kawakami H, Ito H, Takahashi R. Optineurin suppression causes neuronal cell death via NF-κB pathway. Journal of Neurochemistry. 126: 699-704. PMID 23721573 DOI: 10.1111/Jnc.12326 |
0.331 |
|
| 2013 |
Shodai A, Morimura T, Ido A, Uchida T, Ayaki T, Takahashi R, Kitazawa S, Suzuki S, Shirouzu M, Kigawa T, Muto Y, Yokoyama S, Takahashi R, Kitahara R, Ito H, et al. Aberrant assembly of RNA recognition motif 1 links to pathogenic conversion of TAR DNA-binding protein of 43 kDa (TDP-43). The Journal of Biological Chemistry. 288: 14886-905. PMID 23558684 DOI: 10.1074/Jbc.M113.451849 |
0.563 |
|
| 2013 |
Matsui H, Sato F, Sato S, Koike M, Taruno Y, Saiki S, Funayama M, Ito H, Taniguchi Y, Uemura N, Toyoda A, Sakaki Y, Takeda S, Uchiyama Y, Hattori N, et al. ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons. Febs Letters. 587: 1316-25. PMID 23499937 DOI: 10.1016/J.Febslet.2013.02.046 |
0.359 |
|
| 2013 |
Matsui H, Gavinio R, Asano T, Uemura N, Ito H, Taniguchi Y, Kobayashi Y, Maki T, Shen J, Takeda S, Uemura K, Yamakado H, Takahashi R. PINK1 and Parkin complementarily protect dopaminergic neurons in vertebrates. Human Molecular Genetics. 22: 2423-34. PMID 23449626 DOI: 10.1093/Hmg/Ddt095 |
0.305 |
|
| 2013 |
Asayama S, Wate R, Kaneko S, Asayama T, Oki M, Tsuge A, Nagashima M, Morita J, Nakamura S, Nakamura M, Nishii M, Fujita K, Saito A, Nakano S, Ito H, et al. Levodopa challenge test and (123) I-metaiodobenzylguanidine scintigraphy for diagnosing Parkinson's disease. Acta Neurologica Scandinavica. 128: 160-5. PMID 23410225 DOI: 10.1111/Ane.12104 |
0.512 |
|
| 2013 |
Nakamura M, Kaneko S, Ito H, Jiang S, Fujita K, Wate R, Nakano S, Fujisawa J, Kusaka H. Activation of transforming growth factor-β/Smad signaling reduces aggregate formation of mislocalized TAR DNA-binding protein-43. Neuro-Degenerative Diseases. 11: 182-93. PMID 22797246 DOI: 10.1159/000338151 |
0.548 |
|
| 2013 |
Nakamura M, Kaneko S, Wate R, Asayama S, Nakamura Y, Fujita K, Ito H, Kusaka H. Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP-43-positive inclusions of amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology. 39: 144-56. PMID 22435645 DOI: 10.1111/J.1365-2990.2012.01270.X |
0.581 |
|
| 2013 |
Nakamura M, Kaneko S, Ito H, Jiang S, Fujita K, Wate R, Nakano S, Fujisawa J, Kusaka H, Flunkert S, Hierzer M, Löffler T, Rabl R, Neddens J, Duller S, et al. Contents Vol. 11, 2013 Neurodegenerative Diseases. 11. DOI: 10.1159/000350668 |
0.455 |
|
| 2012 |
Shodai A, Ido A, Fujiwara N, Ayaki T, Morimura T, Oono M, Uchida T, Takahashi R, Ito H, Urushitani M. Conserved acidic amino acid residues in a second RNA recognition motif regulate assembly and function of TDP-43. Plos One. 7: e52776. PMID 23300771 DOI: 10.1371/Journal.Pone.0052776 |
0.531 |
|
| 2012 |
Tashiro Y, Urushitani M, Inoue H, Koike M, Uchiyama Y, Komatsu M, Tanaka K, Yamazaki M, Abe M, Misawa H, Sakimura K, Ito H, Takahashi R. Motor neuron-specific disruption of proteasomes, but not autophagy, replicates amyotrophic lateral sclerosis. The Journal of Biological Chemistry. 287: 42984-94. PMID 23095749 DOI: 10.1074/Jbc.M112.417600 |
0.37 |
|
| 2012 |
Ishiura H, Sako W, Yoshida M, Kawarai T, Tanabe O, Goto J, Takahashi Y, Date H, Mitsui J, Ahsan B, Ichikawa Y, Iwata A, Yoshino H, Izumi Y, Fujita K, ... ... Ito H, et al. The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement. American Journal of Human Genetics. 91: 320-9. PMID 22883144 DOI: 10.1016/J.Ajhg.2012.07.014 |
0.588 |
|
| 2012 |
Egawa N, Kitaoka S, Tsukita K, Naitoh M, Takahashi K, Yamamoto T, Adachi F, Kondo T, Okita K, Asaka I, Aoi T, Watanabe A, Yamada Y, Morizane A, Takahashi J, ... ... Ito H, et al. Drug screening for ALS using patient-specific induced pluripotent stem cells. Science Translational Medicine. 4: 145ra104. PMID 22855461 DOI: 10.1126/Scitranslmed.3004052 |
0.604 |
|
| 2012 |
Sako W, Ito H, Yoshida M, Koizumi H, Kamada M, Fujita K, Hashizume Y, Izumi Y, Kaji R. Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations. Clinical Neuropathology. 31: 418-23. PMID 22762947 DOI: 10.5414/Np300493 |
0.503 |
|
| 2012 |
Honjo Y, Ito H, Horibe T, Shimada H, Nakanishi A, Mori H, Takahashi R, Kawakami K. Derlin-1-immunopositive inclusions in patients with Alzheimer's disease. Neuroreport. 23: 611-5. PMID 22627700 DOI: 10.1097/Wnr.0B013E3283552A75 |
0.324 |
|
| 2012 |
Kawamoto Y, Ito H, Ihara M, Takahashi R. Immunohistochemical localization of X-linked inhibitor of apoptosis protein in brainstem-type and cortical Lewy bodies. Neuroreport. 23: 162-7. PMID 22273571 DOI: 10.1097/Wnr.0B013E32834F4066 |
0.329 |
|
| 2012 |
Okamoto Y, Yamamoto T, Kalaria RN, Senzaki H, Maki T, Hase Y, Kitamura A, Washida K, Yamada M, Ito H, Tomimoto H, Takahashi R, Ihara M. Cerebral hypoperfusion accelerates cerebral amyloid angiopathy and promotes cortical microinfarcts. Acta Neuropathologica. 123: 381-94. PMID 22170742 DOI: 10.1007/S00401-011-0925-9 |
0.579 |
|
| 2012 |
Kitamura A, Fujita Y, Oishi N, Kalaria RN, Washida K, Maki T, Okamoto Y, Hase Y, Yamada M, Takahashi J, Ito H, Tomimoto H, Fukuyama H, Takahashi R, Ihara M. Selective white matter abnormalities in a novel rat model of vascular dementia. Neurobiology of Aging. 33: 1012.e25-35. PMID 22133276 DOI: 10.1016/J.Neurobiolaging.2011.10.033 |
0.383 |
|
| 2012 |
Yamashita H, Fujimori N, Ito H, Iguchi Y, Atsuta N, Tanaka F, Sobue G, Takahashi R, Yamanaka K. Microarray Analysis in Spinal Cords of Sporadic ALS Patients with Cell-Type Specific Transcriptome (P05.168) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.168 |
0.364 |
|
| 2012 |
Nakamura M, Kaneko S, Ito H, Fujisawa J, Kusaka H. Activation of Transforming Growth Factor-beta/Smad Signaling Reduces Aggregate Formation of Mislocalized TAR DNA Binding Protein-43 (P03.182) Neurology. 78: P03.182-P03.182. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P03.182 |
0.52 |
|
| 2011 |
Okamoto Y, Ihara M, Urushitani M, Yamashita H, Kondo T, Tanigaki A, Oono M, Kawamata J, Ikemoto A, Kawamoto Y, Takahashi R, Ito H. An autopsy case of SOD1-related ALS with TDP-43 positive inclusions. Neurology. 77: 1993-5. PMID 22094482 DOI: 10.1212/Wnl.0B013E31823A0Cfc |
0.68 |
|
| 2011 |
Honjo Y, Kaneko S, Ito H, Horibe T, Nagashima M, Nakamura M, Fujita K, Takahashi R, Kusaka H, Kawakami K. Protein disulfide isomerase-immunopositive inclusions in patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 12: 444-50. PMID 21745122 DOI: 10.3109/17482968.2011.594055 |
0.602 |
|
| 2011 |
Honjo Y, Ito H, Horibe T, Takahashi R, Kawakami K. Protein disulfide isomerase immunopositive glial cytoplasmic inclusions in patients with multiple system atrophy. The International Journal of Neuroscience. 121: 543-50. PMID 21689057 DOI: 10.3109/00207454.2011.585440 |
0.339 |
|
| 2011 |
Okamoto Y, Shirakashi Y, Ihara M, Urushitani M, Oono M, Kawamoto Y, Yamashita H, Shimohama S, Kato S, Hirano A, Tomimoto H, Ito H, Takahashi R. Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model. Plos One. 6: e20427. PMID 21655264 DOI: 10.1371/Journal.Pone.0020427 |
0.643 |
|
| 2011 |
Ito H, Nakamura M, Komure O, Ayaki T, Wate R, Maruyama H, Nakamura Y, Fujita K, Kaneko S, Okamoto Y, Ihara M, Konishi T, Ogasawara K, Hirano A, Kusaka H, et al. Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation. Acta Neuropathologica. 122: 223-9. PMID 21644038 DOI: 10.1007/S00401-011-0842-Y |
0.692 |
|
| 2011 |
Ito H, Fujita K, Nakamura M, Wate R, Kaneko S, Sasaki S, Yamane K, Suzuki N, Aoki M, Shibata N, Togashi S, Kawata A, Mochizuki Y, Mizutani T, Maruyama H, et al. Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease. Acta Neuropathologica. 121: 555-7. PMID 21327942 DOI: 10.1007/S00401-011-0809-Z |
0.746 |
|
| 2011 |
Nakamura M, Ito H, Nakamura Y, Wate R, Kaneko S, Nakano S, Matsumoto S, Kusaka H. Smad ubiquitination regulatory factor-2 in progressive supranuclear palsy. Neuropathology and Applied Neurobiology. 37: 307-14. PMID 20819168 DOI: 10.1111/J.1365-2990.2010.01120.X |
0.561 |
|
| 2011 |
Saito S, Ozaki A, Takahashi M, Ito H, Matsumoto S, Tomimoto H. Clustering of multifocal cerebral infarctions in CADASIL: a case report. Journal of Neurology. 258: 325-7. PMID 20803343 DOI: 10.1007/S00415-010-5727-9 |
0.638 |
|
| 2011 |
Yamashita H, Fujimori N, Kataoka A, Iguchi Y, Atsuta N, Tanaka F, Sobue G, Ito H, Takahashi R, Yamanaka K. Microarray analysis in spinal cords of sporadic ALS patients with cell-type specific transcriptome Neuroscience Research. 71. DOI: 10.1016/J.Neures.2011.07.1276 |
0.341 |
|
| 2010 |
Matsui H, Ito H, Taniguchi Y, Takeda S, Takahashi R. Ammonium chloride and tunicamycin are novel toxins for dopaminergic neurons and induce Parkinson's disease-like phenotypes in medaka fish. Journal of Neurochemistry. 115: 1150-60. PMID 21219329 DOI: 10.1111/J.1471-4159.2010.07012.X |
0.315 |
|
| 2010 |
Kawamoto Y, Ito H, Kobayashi Y, Suzuki Y, Takahashi R. Localization of HtrA2/Omi immunoreactivity in brains affected by Alzheimer's disease. Neuroreport. 21: 1121-5. PMID 20938363 DOI: 10.1097/Wnr.0B013E328340A731 |
0.327 |
|
| 2010 |
Matsui H, Ito H, Taniguchi Y, Inoue H, Takeda S, Takahashi R. Proteasome inhibition in medaka brain induces the features of Parkinson's disease. Journal of Neurochemistry. 115: 178-87. PMID 20649841 DOI: 10.1111/J.1471-4159.2010.06918.X |
0.309 |
|
| 2010 |
Washida K, Ihara M, Nishio K, Fujita Y, Maki T, Yamada M, Takahashi J, Wu X, Kihara T, Ito H, Tomimoto H, Takahashi R. Nonhypotensive dose of telmisartan attenuates cognitive impairment partially due to peroxisome proliferator-activated receptor-gamma activation in mice with chronic cerebral hypoperfusion. Stroke; a Journal of Cerebral Circulation. 41: 1798-806. PMID 20595663 DOI: 10.1161/Strokeaha.110.583948 |
0.403 |
|
| 2010 |
Honjo Y, Ito H, Horibe T, Takahashi R, Kawakami K. Protein disulfide isomerase-immunopositive inclusions in patients with Alzheimer disease. Brain Research. 1349: 90-6. PMID 20550946 DOI: 10.1016/J.Brainres.2010.06.016 |
0.317 |
|
| 2010 |
Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, et al. Mutations of optineurin in amyotrophic lateral sclerosis. Nature. 465: 223-6. PMID 20428114 DOI: 10.1038/Nature08971 |
0.725 |
|
| 2010 |
Kawamoto Y, Ito H, Kobayashi Y, Suzuki Y, Akiguchi I, Fujimura H, Sakoda S, Kusaka H, Hirano A, Takahashi R. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology. 36: 331-44. PMID 20202124 DOI: 10.1111/J.1365-2990.2010.01075.X |
0.69 |
|
| 2010 |
Washida K, Ihara M, Nishio K, Fujita Y, Maki T, Yamada M, Takahashi J, Wu X, Kihara T, Ito H, Tomimoto H, Takahashi R. Nonhypotensive dose of telmisartan attenuates cognitive impairment partially due to PPAR-γ activation in mice with chronic cerebral hypoperfusion Neuroscience Research. 68. DOI: 10.1016/J.Neures.2010.07.1342 |
0.381 |
|
| 2009 |
Kinoshita Y, Ito H, Hirano A, Fujita K, Wate R, Nakamura M, Kaneko S, Nakano S, Kusaka H. Nuclear contour irregularity and abnormal transporter protein distribution in anterior horn cells in amyotrophic lateral sclerosis. Journal of Neuropathology and Experimental Neurology. 68: 1184-92. PMID 19816199 DOI: 10.1097/Nen.0B013E3181Bc3Bec |
0.66 |
|
| 2009 |
Ohnishi S, Ito H, Suzuki Y, Adachi Y, Wate R, Zhang J, Nakano S, Kusaka H, Ikehara S. Intra-bone marrow-bone marrow transplantation slows disease progression and prolongs survival in G93A mutant SOD1 transgenic mice, an animal model mouse for amyotrophic lateral sclerosis. Brain Research. 1296: 216-24. PMID 19686706 DOI: 10.1016/J.Brainres.2009.08.012 |
0.511 |
|
| 2009 |
Kamada M, Maruyama H, Tanaka E, Morino H, Wate R, Ito H, Kusaka H, Kawano Y, Miki T, Nodera H, Izumi Y, Kaji R, Kawakami H. Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 284: 69-71. PMID 19411082 DOI: 10.1016/J.Jns.2009.04.017 |
0.577 |
|
| 2009 |
Shinde A, Kunieda T, Kinoshita Y, Wate R, Nakano S, Ito H, Yamada M, Kitamoto T, Nakamura Y, Matsumoto S, Kusaka H. The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD). Neuropathology : Official Journal of the Japanese Society of Neuropathology. 29: 713-9. PMID 19389077 DOI: 10.1111/J.1440-1789.2009.01006.X |
0.554 |
|
| 2009 |
Washida K, Ihara M, Takahashi J, Ito H, Tomimoto H, Takahashi R. The effect of vascular progenitor cells on chronic cerebral hypoperfusion mouse model Neuroscience Research. 65. DOI: 10.1016/J.Neures.2009.09.585 |
0.38 |
|
| 2008 |
Ito H, Wate R, Zhang J, Ohnishi S, Kaneko S, Ito H, Nakano S, Kusaka H. Treatment with edaravone, initiated at symptom onset, slows motor decline and decreases SOD1 deposition in ALS mice. Experimental Neurology. 213: 448-55. PMID 18718468 DOI: 10.1016/J.Expneurol.2008.07.017 |
0.566 |
|
| 2008 |
Fujita K, Ito H, Nakano S, Kinoshita Y, Wate R, Kusaka H. Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease. Acta Neuropathologica. 116: 439-45. PMID 18642007 DOI: 10.1007/S00401-008-0415-X |
0.561 |
|
| 2008 |
Shinde A, Nakano S, Sugawara M, Toyoshima I, Ito H, Tanaka K, Kusaka H. Expression of caveolar components in primary desminopathy. Neuromuscular Disorders : Nmd. 18: 215-9. PMID 18343114 DOI: 10.1016/J.Nmd.2007.12.006 |
0.539 |
|
| 2008 |
Nakamura M, Ito H, Wate R, Nakano S, Hirano A, Kusaka H. Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model. Acta Neuropathologica. 115: 327-34. PMID 18210139 DOI: 10.1007/S00401-007-0337-Z |
0.684 |
|
| 2008 |
Nakano S, Shinde A, Fujita K, Ito H, Kusaka H. Histone H1 is released from myonuclei and present in rimmed vacuoles with DNA in inclusion body myositis. Neuromuscular Disorders : Nmd. 18: 27-33. PMID 17888663 DOI: 10.1016/J.Nmd.2007.08.005 |
0.501 |
|
| 2007 |
Ito H, Ito H, Fujita K, Kinoshita Y, Takanashi Y, Kusaka H. Phrenic nerve conduction in the early stage of Guillain-Barre syndrome might predict the respiratory failure. Acta Neurologica Scandinavica. 116: 255-8. PMID 17824905 DOI: 10.1111/J.1600-0404.2007.00874.X |
0.495 |
|
| 2007 |
Ito H, Ito H, Nakano S, Kusaka H. Low-dose subcutaneous injection of botulinum toxin type A for facial synkinesis and hyperlacrimation. Acta Neurologica Scandinavica. 115: 271-4. PMID 17376126 DOI: 10.1111/J.1600-0404.2006.00746.X |
0.502 |
|
| 2006 |
Zhang J, Ito H, Wate R, Ohnishi S, Nakano S, Kusaka H. Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis. Acta Neuropathologica. 112: 673-80. PMID 16957927 DOI: 10.1007/S00401-006-0130-4 |
0.586 |
|
| 2006 |
Ito H, Ito H, Tanaka N, Asayama S, Nakano S, Kusaka H. [Bilateral gustatory disturbance associated with left putaminal hemorrhage]. Rinshå Shinkeigaku = Clinical Neurology. 46: 288-90. PMID 16768099 |
0.445 |
|
| 2005 |
Wate R, Ito H, Zhang JH, Ohnishi S, Nakano S, Kusaka H. Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis. Acta Neuropathologica. 110: 557-62. PMID 16231159 DOI: 10.1007/S00401-005-1080-Y |
0.581 |
|
| 2005 |
Nakano S, Shinde A, Ito H, Ito H, Kusaka H. Messenger RNA degradation may be inhibited in sporadic inclusion body myositis. Neurology. 65: 420-5. PMID 16087907 DOI: 10.1212/01.Wnl.0000171341.76482.15 |
0.519 |
|
| 2005 |
Fujita K, Nakano S, Yamamoto H, Ito H, Ito H, Goto Y, Kusaka H. [An adult case of congenital fiber type disproportion (CFTD) with cardiomyopathy]. Rinshå Shinkeigaku = Clinical Neurology. 45: 380-2. PMID 15960177 |
0.453 |
|
| 2005 |
Wate R, Takahashi S, Ito H, Kusaka H, Kubota Y, Suetomi K, Sato H, Okayasu R. Radio-sensitivity of the cells from amyotrophic lateral sclerosis model mice transfected with human mutant SOD1. Journal of Radiation Research. 46: 67-73. PMID 15802861 DOI: 10.1269/Jrr.46.67 |
0.557 |
|
| 2005 |
Ito H, Ito H, Nagano M, Nakano S, Shigeyoshi Y, Kusaka H. In situ identification of hepatitis C virus RNA in muscle. Neurology. 64: 1073-5. PMID 15781833 DOI: 10.1212/01.Wnl.0000154605.02737.Fe |
0.48 |
|
| 2004 |
Ito H, Kusaka H. [Cognitive impairment induced by sedatives/hypnotics]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 62: 456-60. PMID 15011405 |
0.395 |
|
| 2003 |
Nakano S, Shinde A, Ito H, Ito H, Kusaka H. MAP kinase phosphatase-1 is induced in abnormal fibers in inclusion body myositis. Neurology. 61: 322-6. PMID 12913191 DOI: 10.1212/01.Wnl.0000076479.29079.10 |
0.5 |
|
| 2003 |
Tamaru Y, Nakashita M, Ito H, Okumura R, Matsumoto S, Imai T. Spontaneous remission of a massive CNS inflammation with eosinophilic infiltrate. Internal Medicine (Tokyo, Japan). 42: 424-7. PMID 12793714 DOI: 10.2169/Internalmedicine.42.424 |
0.461 |
|
| 2003 |
Ito H, Yoshika M, Ohnishi S, Iimuro R, Yagi A, Nakano S, Ito H, Kusaka H. [Intractable hiccups treated with mexiletine hydrochloride]. Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine. 92: 316-7. PMID 12652738 |
0.409 |
|
| 2002 |
Ito H, Nakano S, Ito H, Kusaka H. Our Experience of Muscle Afferent Block for dystonia and spasticity The Journal of Kansai Medical University. 54: 130-134. DOI: 10.5361/Jkmu1956.54.2-4_130 |
0.471 |
|
| 1998 |
Tamaru Y, Hirano M, Ito H, Kawamura J, Matsumoto S, Imai T, Ueno S. Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene. Journal of Neurology, Neurosurgery, and Psychiatry. 64: 469-73. PMID 9576537 DOI: 10.1136/Jnnp.64.4.469 |
0.456 |
|
| 1998 |
Kobata H, Kondo A, Iwasaki K, Kusaka H, Ito H, Sawada S. Chordoid meningioma in a child. Case report. Journal of Neurosurgery. 88: 319-23. PMID 9452243 DOI: 10.3171/Jns.1998.88.2.0319 |
0.52 |
|
| 1997 |
Tamaru Y, Hirano M, Kusaka H, Ito H, Imai T, Ueno S. alpha-Tocopherol transfer protein gene: exon skipping of all transcripts causes ataxia. Neurology. 49: 584-8. PMID 9270601 DOI: 10.1212/Wnl.49.2.584 |
0.596 |
|
| 1997 |
Ii K, Ito H, Tanaka K, Hirano A. Immunocytochemical co-localization of the proteasome in ubiquitinated structures in neurodegenerative diseases and the elderly. Journal of Neuropathology and Experimental Neurology. 56: 125-31. PMID 9034365 DOI: 10.1097/00005072-199702000-00002 |
0.536 |
|
| 1997 |
Hirano M, Tamaru Y, Ito H, Matsumoto S, Imai T, Ueno S. Mutant GTP cyclohydrolase I mRNA levels contribute to dopa-responsive dystonia onset. Annals of Neurology. 40: 796-8. PMID 8957022 DOI: 10.1002/Ana.410400517 |
0.479 |
|
| 1996 |
Ito H, Kusaka H, Matsumoto S, Imai T. Striatal efferent involvement and its correlation to levodopa efficacy in patients with multiple system atrophy. Neurology. 47: 1291-9. PMID 8909445 DOI: 10.1212/Wnl.47.5.1291 |
0.557 |
|
| 1996 |
Matsumoto S, Kusaka H, Ito H, Imai T. Golgi apparatus and intraneuronal inclusions of anterior horn cells in amyotrophic lateral sclerosis: an immunohistochemical study. Acta Neuropathologica. 91: 603-7. PMID 8781659 DOI: 10.1007/S004010050473 |
0.601 |
|
| 1996 |
Kaneko S, Ito H, Kusaka H, Imai T, Nishimura T, Yoshikawa H. Peripheral myelin protein-22 gene deletion in two unrelated Japanese pedigrees with hereditary neuropathy with liability to pressure palsies. Muscle & Nerve. 19: 675-6. PMID 8618572 DOI: 10.1002/mus.880190502 |
0.549 |
|
| 1995 |
Ito H, Kusaka H, Matsumoto S, Imai T. Topographic involvement of the striatal efferents in basal ganglia of patients with adult-onset motor neuron disease with basophilic inclusions. Acta Neuropathologica. 89: 513-8. PMID 7545858 DOI: 10.1007/Bf00571505 |
0.587 |
|
| 1994 |
Matsumoto S, Goto S, Kusaka H, Ito H, Imai T. Synaptic pathology of spinal anterior horn cells in amyotrophic lateral sclerosis: an immunohistochemical study. Journal of the Neurological Sciences. 125: 180-5. PMID 7807164 DOI: 10.1016/0022-510X(94)90032-9 |
0.686 |
|
| 1994 |
Ito H, Hirano A. Comparative study of spinal cord ubiquitin expression in post-poliomyelitis and sporadic amyotrophic lateral sclerosis. Acta Neuropathologica. 87: 425-9. PMID 7517092 DOI: 10.1007/Bf00313613 |
0.527 |
|
| 1993 |
Ito H, Goto S, Sakamoto S, Hirano A. Striosomal arrangement of met-enkephalin and substance P expression in parkinsonism-dementia complex on Guam. Acta Neuropathologica. 85: 390-3. PMID 7683167 DOI: 10.1007/Bf00334449 |
0.581 |
|
| 1992 |
Kato S, Hirano A, Llena JF, Ito H, Yen SH. Ultrastructural identification of neurofibrillary tangles in the spinal cords in Guamanian amyotrophic lateral sclerosis and parkinsonism-dementia complex on Guam. Acta Neuropathologica. 83: 277-82. PMID 1557958 DOI: 10.1007/Bf00296790 |
0.579 |
|
| 1992 |
Kusaka H, Imai T, Matsumoto S, Ito H, Yamasaki M. Myelination of two axons by a single Schwann cell. Acta Neuropathologica. 84: 574-6. PMID 1462770 DOI: 10.1007/BF00304478 |
0.417 |
|
| 1991 |
Kato S, Nakamura H, Hirano A, Ito H, Llena JF, Yen SH. Argyrophilic ubiquitinated cytoplasmic inclusions of Leu-7-positive glial cells in olivopontocerebellar atrophy (multiple system atrophy). Acta Neuropathologica. 82: 488-93. PMID 1723828 DOI: 10.1007/Bf00293383 |
0.63 |
|
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