| Year |
Citation |
Score |
| 2021 |
Itani K, Nakamura M, Wate R, Kaneko S, Fujita K, Iida S, Morise S, Murakami A, Kunieda T, Takenouchi N, Yakushiji Y, Kusaka H. Efficacy and safety of tacrolimus as long-term monotherapy for myasthenia gravis. Neuromuscular Disorders : Nmd. PMID 33903022 DOI: 10.1016/j.nmd.2021.02.010 |
0.43 |
|
| 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 |
0.608 |
|
| 2017 |
Oki M, Kaneko S, Morise S, Takenouchi N, Hashizume T, Tsuge A, Nakamura M, Wate R, Kusaka H. Zonisamide ameliorates levodopa-induced dyskinesia and reduces expression of striatal genes in Parkinson model rats. Neuroscience Research. PMID 28577977 DOI: 10.1016/J.Jns.2017.08.1675 |
0.481 |
|
| 2017 |
Tsuge A, Kaneko S, Wate R, Oki M, Nagashima M, Asayama S, Nakamura M, Fujita K, Saito A, Takenouchi N, Kusaka H. Weight loss in the early stage of progressive supranuclear palsy. Brain and Behavior. 7: e00616. PMID 28239526 DOI: 10.1002/Brb3.616 |
0.498 |
|
| 2017 |
Itani K, Wate R, Kaneko S, Fujita K, Iida S, Morise S, Murakami A, Oki M, Tsuge A, Miyake K, Nakamura M, Kunieda T, Kusaka H. Long-term efficacy and safety of tacrolimus monotherapy for myasthenia gravis Journal of the Neurological Sciences. 381: 467. DOI: 10.1016/J.Jns.2017.08.3525 |
0.443 |
|
| 2016 |
Oki M, Hori S, Asayama S, Wate R, Kaneko S, Kusaka H. Early-onset Parkinson's Disease Associated with Chromosome 22q11.2 Deletion Syndrome. Internal Medicine (Tokyo, Japan). 55: 303-5. PMID 26831029 DOI: 10.2169/Internalmedicine.55.5485 |
0.512 |
|
| 2015 |
Iida S, Nakamura M, Wate R, Kaneko S, Kusaka H. Successful treatment of paroxysmal tonic spasms with topiramate in a patient with neuromyelitis optica. Multiple Sclerosis and Related Disorders. 4: 457-9. PMID 26346795 DOI: 10.1016/J.Msard.2015.07.011 |
0.48 |
|
| 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 |
0.622 |
|
| 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 |
0.495 |
|
| 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 |
0.56 |
|
| 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 |
0.605 |
|
| 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 |
0.444 |
|
| 2013 |
Tsuge A, Kaneko S, Wate R, Yamazaki F, Kusaka H. Case of acquired idiopathic cold-induced hyperhidrosis Neurology and Clinical Neuroscience. 1: 114-115. DOI: 10.1111/J.2049-4173.2013.00026.X |
0.498 |
|
| 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 |
0.7 |
|
| 2011 |
Nishii M, Nakano S, Nakamura S, Wate R, Shinde A, Kaneko S, Kusaka H. Myonuclear breakdown in sporadic inclusion body myositis is accompanied by DNA double strand breaks. Neuromuscular Disorders : Nmd. 21: 345-52. PMID 21353553 DOI: 10.1016/J.Nmd.2011.02.004 |
0.494 |
|
| 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 |
0.648 |
|
| 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 |
0.566 |
|
| 2009 |
Nakamura S, Wate R, Shinde A, Asayama S, Nakano S, Kusaka H. [A case of cerebellar syndrome associated with HIV infection]. Rinshå Shinkeigaku = Clinical Neurology. 49: 651-5. PMID 19999147 DOI: 10.5692/Clinicalneurol.49.651 |
0.499 |
|
| 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 |
0.682 |
|
| 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 |
0.713 |
|
| 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 |
0.58 |
|
| 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 |
0.546 |
|
| 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 |
0.732 |
|
| 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 |
0.582 |
|
| 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 |
0.726 |
|
| 2007 |
Hirano A, Wate R. Diagnostic clues and more from photographs. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 27: 1-9. PMID 17319278 DOI: 10.1111/J.1440-1789.2006.00764.X |
0.486 |
|
| 2006 |
Ito H, Kawakami H, Wate R, Matsumoto S, Imai T, Hirano A, Kusaka H. Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats. Neurology. 67: 1479-81. PMID 17060579 DOI: 10.1212/01.Wnl.0000240256.13633.7B |
0.646 |
|
| 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 |
0.742 |
|
| 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 |
0.738 |
|
| 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 |
0.598 |
|
| Show low-probability matches. |