Hidefumi Ito, MD, PhD - Publications

Affiliations: 
Neurology Kansai Medical University, Hirakata-shi, Ōsaka-fu, Japan 
Website:
http://www.med.kyoto-u.ac.jp/E/grad_school/introduction/1605/

87 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  1
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  0.52
2019 Nakayama Y, Sakamoto S, Tsuji K, Ayaki T, Tokunaga F, Ito H. Identification of linear polyubiquitin chain immunoreactivity in tau pathology of Alzheimer's disease. Neuroscience Letters. 703: 53-57. PMID 30885635 DOI: 10.1016/j.neulet.2019.03.017  0.44
2019 Kinboshi M, Shimizu S, Mashimo T, Serikawa T, Ito H, Ikeda A, Takahashi R, Ohno Y. Down-Regulation of Astrocytic Kir4.1 Channels during the Audiogenic Epileptogenesis in () Mutant Rats. International Journal of Molecular Sciences. 20. PMID 30813600 DOI: 10.3390/ijms20051013  0.44
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  0.44
2018 Hosokawa M, Murata KY, Hironishi M, Koh J, Nishioka K, Nakao N, Ito H. Superficial siderosis associated with duplicated dura mater detected by CISS reverse MRI. Journal of the Neurological Sciences. 392: 38-43. PMID 30097152 DOI: 10.1016/j.jns.2018.07.001  0.84
2018 Shima T, Yamamoto Y, Kanazawa N, Murata KY, Ito H, Kondo T, Yuan J, Hashiguchi A, Takashima H, Furukawa F. Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II. The Journal of Dermatology. PMID 29701257 DOI: 10.1111/1346-8138.14336  0.84
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  1
2017 Honjo Y, Ayaki T, Horibe T, Ito H, Takahashi R, Kawakami K. FKBP12-immunopositive inclusions in patients with α-synucleinopathies. Brain Research. PMID 29246765 DOI: 10.1016/j.brainres.2017.12.012  0.44
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  0.44
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  0.52
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  0.32
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  0.84
2016 Kawamoto Y, Ayaki T, Urushitani M, Ito H, Takahashi R. Activated caspase-9 immunoreactivity in glial and neuronal cytoplasmic inclusions in multiple system atrophy. Neuroscience Letters. PMID 27345387 DOI: 10.1016/j.neulet.2016.06.036  0.48
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  0.48
2016 Nagashima Y, Kondo T, Sakata M, Koh J, Ito H. Effects of soybean ingestion on pharmacokinetics of levodopa and motor symptoms of Parkinson's disease - In relation to the effects of Mucuna pruriens. Journal of the Neurological Sciences. 361: 229-34. PMID 26810548 DOI: 10.1016/j.jns.2016.01.005  0.48
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  0.52
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  0.44
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  0.84
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  1
2014 Murata KY, Ito H. [The etiology and pathogenesis of sporadic inclusion body myositis]. Brain and Nerve = Shinkei KenkyÅ« No Shinpo. 66: 1385-94. PMID 25407074 DOI: 10.11477/mf.1416200044  0.84
2014 Kitajima Y, Tashiro Y, Suzuki N, Warita H, Kato M, Tateyama M, Ando R, Izumi R, Yamazaki M, Abe M, Sakimura K, Ito H, Urushitani M, Nagatomi R, Takahashi R, et al. Proteasome dysfunction induces muscle growth defects and protein aggregation. Journal of Cell Science. 127: 5204-17. PMID 25380823 DOI: 10.1242/jcs.150961  0.48
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  0.44
2014 Teraguchi M, Yamada H, Yoshida M, Nakayama Y, Kondo T, Ito H, Terada M, Kaneoke Y. Contrast enrichment of spinal cord MR imaging using a ratio of T1-weighted and T2-weighted signals. Journal of Magnetic Resonance Imaging : Jmri. 40: 1199-207. PMID 24395471 DOI: 10.1002/jmri.24456  0.44
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  0.44
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  0.44
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  0.52
2014 Murata KY, Sugie H, Nishino I, Kondo T, Ito H. A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency. Muscle & Nerve. 49: 295-6. PMID 23966064 DOI: 10.1002/mus.24055  0.84
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  0.52
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  1
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  0.84
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  0.44
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  0.84
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  0.44
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  0.52
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  1
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  0.84
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  0.84
2012 Okada Y, Ayaki T, Matsumoto R, Ito H, Takahashi R, Nakano S. [Patient of myofibrillar myopathy associated with muscle cramp and distal muscle involvement]. Rinshō Shinkeigaku = Clinical Neurology. 52: 774-7. PMID 23064629 DOI: DN/JST.JSTAGE/clinicalneurol/52.774  0.52
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  0.84
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  0.84
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  0.84
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  0.44
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  0.52
2012 Kasahara S, Miki Y, Kanagaki M, Kondo T, Yamamoto A, Morimoto E, Okada T, Ito H, Takahashi R, Togashi K. "Hot cross bun" sign in multiple system atrophy with predominant cerebellar ataxia: a comparison between proton density-weighted imaging and T2-weighted imaging. European Journal of Radiology. 81: 2848-52. PMID 22209432 DOI: 10.1016/j.ejrad.2011.12.012  0.44
2012 Maesako M, Uemura K, Kubota M, Kuzuya A, Sasaki K, Asada M, Watanabe K, Hayashida N, Ihara M, Ito H, Shimohama S, Kihara T, Kinoshita A. Environmental enrichment ameliorated high-fat diet-induced Aβ deposition and memory deficit in APP transgenic mice. Neurobiology of Aging. 33: 1011.e11-23. PMID 22197104 DOI: 10.1016/j.neurobiolaging.2011.10.028  0.84
2012 Hase Y, Okamoto Y, Fujita Y, Kitamura A, Nakabayashi H, Ito H, Maki T, Washida K, Takahashi R, Ihara M. Cilostazol, a phosphodiesterase inhibitor, prevents no-reflow and hemorrhage in mice with focal cerebral ischemia. Experimental Neurology. 233: 523-33. PMID 22173318 DOI: 10.1016/j.expneurol.2011.11.038  0.52
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  0.84
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  0.84
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  1
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  0.44
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  0.84
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  1
2011 Maki T, Wakita H, Mase M, Itagaki I, Saito N, Ono F, Adachi K, Ito H, Takahashi R, Ihara M, Tomimoto H. Watershed infarcts in a multiple microembolic model of monkey. Neuroscience Letters. 499: 80-3. PMID 21640789 DOI: 10.1016/j.neulet.2011.05.036  0.84
2011 Maki T, Ihara M, Fujita Y, Nambu T, Harada H, Ito H, Nakao K, Tomimoto H, Takahashi R. Angiogenic roles of adrenomedullin through vascular endothelial growth factor induction. Neuroreport. 22: 442-7. PMID 21558971 DOI: 10.1097/WNR.0b013e32834757e4  0.52
2011 Maki T, Ihara M, Fujita Y, Nambu T, Miyashita K, Yamada M, Washida K, Nishio K, Ito H, Harada H, Yokoi H, Arai H, Itoh H, Nakao K, Takahashi R, et al. Angiogenic and vasoprotective effects of adrenomedullin on prevention of cognitive decline after chronic cerebral hypoperfusion in mice. Stroke; a Journal of Cerebral Circulation. 42: 1122-8. PMID 21393586 DOI: 10.1161/STROKEAHA.110.603399  0.52
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  0.84
2011 Yamada M, Ihara M, Okamoto Y, Maki T, Washida K, Kitamura A, Hase Y, Ito H, Takao K, Miyakawa T, Kalaria RN, Tomimoto H, Takahashi R. The influence of chronic cerebral hypoperfusion on cognitive function and amyloid β metabolism in APP overexpressing mice. Plos One. 6: e16567. PMID 21305033 DOI: 10.1371/journal.pone.0016567  0.84
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  0.32
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  0.44
2010 Fujita Y, Ihara M, Ushiki T, Hirai H, Kizaka-Kondoh S, Hiraoka M, Ito H, Takahashi R. Early protective effect of bone marrow mononuclear cells against ischemic white matter damage through augmentation of cerebral blood flow. Stroke; a Journal of Cerebral Circulation. 41: 2938-43. PMID 20947840 DOI: 10.1161/STROKEAHA.110.596379  0.52
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  0.44
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  0.44
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  0.84
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  0.44
2010 Nishio K, Ihara M, Yamasaki N, Kalaria RN, Maki T, Fujita Y, Ito H, Oishi N, Fukuyama H, Miyakawa T, Takahashi R, Tomimoto H. A mouse model characterizing features of vascular dementia with hippocampal atrophy. Stroke; a Journal of Cerebral Circulation. 41: 1278-84. PMID 20448204 DOI: 10.1161/STROKEAHA.110.581686  0.84
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  0.84
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  1
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  1
2009 Okamoto Y, Ihara M, Fujita Y, Ito H, Takahashi R, Tomimoto H. Cortical microinfarcts in Alzheimer's disease and subcortical vascular dementia. Neuroreport. 20: 990-6. PMID 19483658 DOI: 10.1097/WNR.0b013e32832d2e6a  0.52
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  1
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  0.84
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  1
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  1
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  1
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  1
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  1
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  1
2006 Ito H, Ito H, Tanaka N, Asayama S, Nakano S, Kusaka H. [Bilateral gustatory disturbance associated with left putaminal hemorrhage]. Rinshō Shinkeigaku = Clinical Neurology. 46: 288-90. PMID 16768099  1
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  1
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]. Rinshō Shinkeigaku = Clinical Neurology. 45: 380-2. PMID 15960177  1
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: JST.JSTAGE/jrr/46.67  1
2005 Minamino K, Adachi Y, Okigaki M, Ito H, Togawa Y, Fujita K, Tomita M, Suzuki Y, Zhang Y, Iwasaki M, Nakano K, Koike Y, Matsubara H, Iwasaka T, Matsumura M, et al. Macrophage colony-stimulating factor (M-CSF), as well as granulocyte colony-stimulating factor (G-CSF), accelerates neovascularization. Stem Cells (Dayton, Ohio). 23: 347-54. PMID 15749929 DOI: 10.1634/stemcells.2004-0190  0.44
2004 Ito H, Kusaka H. [Cognitive impairment induced by sedatives/hypnotics]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 62: 456-60. PMID 15011405  1
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  0.32
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  1
2003 Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6. American Journal of Human Genetics. 72: 704-9. PMID 12545428 DOI: 10.1086/367775  0.4
Show low-probability matches.