| 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 |
0.676 |
|
| 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, ... ... Kusaka 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 |
0.537 |
|
| 2019 |
Nakamura M, Kaneko S, Dickson DW, Kusaka H. Aberrant Accumulation of BRCA1 in Alzheimer Disease and Other Tauopathies. Journal of Neuropathology and Experimental Neurology. PMID 31750914 DOI: 10.1093/Jnen/Nlz107 |
0.354 |
|
| 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 |
0.551 |
|
| 2018 |
Nakamura M, Ueki S, Kubo M, Yagi H, Sasaki R, Okada Y, Akiguchi I, Kusaka H, Kondo T. Two cases of sporadic adult-onset neuronal intranuclear inclusion disease preceded by urinary disturbance for many years. Journal of the Neurological Sciences. 392: 89-93. PMID 30031993 DOI: 10.1016/J.Jns.2018.07.012 |
0.343 |
|
| 2018 |
Ueki S, Nakamura M, Sasaki R, Okada Y, Yoshikawa K, Kusunoki S, Ishii K, Kusaka H, Kondo T. Beneficial Effect of Bendamustine in a Patient with Anti-MAG/SGPG Neuropathy and Bing-Neel Syndrome Associated with Waldenström Macroglobulinemia: A Case Report. Case Reports in Neurology. 10: 88-94. PMID 29983700 DOI: 10.1159/000487850 |
0.308 |
|
| 2018 |
Murakami A, Nakamura M, Kaneko S, Lin WL, Dickson DW, Kusaka H. Aberrant accumulation of ErbB4 in progressive supranuclear palsy. Neuropathology and Applied Neurobiology. PMID 29319907 DOI: 10.1111/Nan.12460 |
0.391 |
|
| 2018 |
Kusaka H. 16. Pathomechanisms and Treatments of Motor Neuron Diseases Nihon Naika Gakkai Zasshi. 107: 133a-133a. DOI: 10.2169/Naika.107.133A |
0.318 |
|
| 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 |
0.8 |
|
| 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 |
0.683 |
|
| 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 |
0.699 |
|
| 2017 |
Hayashida A, Li Y, Yoshino H, Nakahara T, Yoritaka A, Nagara Y, Sakiyama Y, Kusaka H, Takiyama Y, Morimoto N, Uchino A, Fujimoto T, Sekijima Y, Tomimoto H, Tsuruta K, et al. Pink1 heterozygous mutations in familial Parkinson's disease Journal of the Neurological Sciences. 381: 161-162. DOI: 10.1016/J.Jns.2017.08.473 |
0.306 |
|
| 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 |
0.664 |
|
| 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 |
0.708 |
|
| 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 |
0.687 |
|
| 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 |
0.779 |
|
| 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 |
0.806 |
|
| 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, ... Kusaka 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 |
0.745 |
|
| 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 |
0.771 |
|
| 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 |
0.787 |
|
| 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 |
0.721 |
|
| 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 |
0.699 |
|
| 2012 |
Neumann M, Valori CF, Ansorge O, Kretzschmar HA, Munoz DG, Kusaka H, Yokota O, Ishihara K, Ang LC, Bilbao JM, Mackenzie IR. Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations. Acta Neuropathologica. 124: 705-16. PMID 22842875 DOI: 10.1007/S00401-012-1020-6 |
0.422 |
|
| 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 |
0.554 |
|
| 2011 |
Neumann M, Bentmann E, Dormann D, Jawaid A, DeJesus-Hernandez M, Ansorge O, Roeber S, Kretzschmar HA, Munoz DG, Kusaka H, Yokota O, Ang LC, Bilbao J, Rademakers R, Haass C, et al. FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations. Brain : a Journal of Neurology. 134: 2595-609. PMID 21856723 DOI: 10.1093/Brain/Awr201 |
0.391 |
|
| 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 |
0.635 |
|
| 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 |
0.815 |
|
| 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 |
0.695 |
|
| 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, ... ... Kusaka 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 |
0.779 |
|
| 2011 |
Mackenzie IR, Munoz DG, Kusaka H, Yokota O, Ishihara K, Roeber S, Kretzschmar HA, Cairns NJ, Neumann M. Distinct pathological subtypes of FTLD-FUS. Acta Neuropathologica. 121: 207-18. PMID 21052700 DOI: 10.1007/S00401-010-0764-0 |
0.352 |
|
| 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 |
0.781 |
|
| 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, ... ... Kusaka H, et al. Mutations of optineurin in amyotrophic lateral sclerosis. Nature. 465: 223-6. PMID 20428114 DOI: 10.1038/Nature08971 |
0.746 |
|
| 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 |
0.71 |
|
| 2010 |
Suzuki N, Aoki M, Tateyama M, Izumi R, Warita H, Itoyama Y, Mori M, Kusaka H, Higuchi I, Kondo T, Uchino M, Kaji R, Nishino I. P2.41 Prevalence of inclusion body myositis (IBM) in Japanese population Neuromuscular Disorders. 20: 631-631. DOI: 10.1016/J.Nmd.2010.07.113 |
0.307 |
|
| 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 |
0.701 |
|
| 2009 |
Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR. FUS pathology in basophilic inclusion body disease. Acta Neuropathologica. 118: 617-27. PMID 19830439 DOI: 10.1007/S00401-009-0598-9 |
0.644 |
|
| 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 |
0.796 |
|
| 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 |
0.751 |
|
| 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 |
0.785 |
|
| 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 |
0.769 |
|
| 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 |
0.775 |
|
| 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 |
0.78 |
|
| 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 |
0.563 |
|
| 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 |
0.814 |
|
| 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 |
0.526 |
|
| 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 |
0.516 |
|
| 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 |
0.527 |
|
| 2007 |
Yuri T, Miki K, Tsukamoto R, Shinde A, Kusaka H, Tsubura A. Autopsy case of desminopathy involving skeletal and cardiac muscle. Pathology International. 57: 32-6. PMID 17199740 DOI: 10.1111/J.1440-1827.2007.02053.X |
0.303 |
|
| 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 |
0.777 |
|
| 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 |
0.786 |
|
| 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 |
0.467 |
|
| 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 |
0.784 |
|
| 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 |
0.487 |
|
| 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 |
0.476 |
|
| 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 |
0.769 |
|
| 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 |
0.434 |
|
| 2004 |
Ito H, Kusaka H. [Cognitive impairment induced by sedatives/hypnotics]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 62: 456-60. PMID 15011405 |
0.414 |
|
| 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 |
0.469 |
|
| 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 |
0.74 |
|
| 2002 |
Fujita Y, Okamoto K, Sakurai A, Kusaka H, Aizawa H, Mihara B, Gonatas NK. The Golgi apparatus is fragmented in spinal cord motor neurons of amyotrophic lateral sclerosis with basophilic inclusions. Acta Neuropathologica. 103: 243-7. PMID 11907804 DOI: 10.1007/S004010100461 |
0.552 |
|
| 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 |
0.49 |
|
| 2000 |
Kato S, Takikawa M, Nakashima K, Hirano A, Cleveland DW, Kusaka H, Shibata N, Kato M, Nakano I, Ohama E. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 1: 163-84. PMID 11464950 DOI: 10.1080/14660820050515160 |
0.757 |
|
| 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 |
0.545 |
|
| 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 |
0.574 |
|
| 1996 |
Matsumoto S, Kusaka H, Ito H, Shibata N, Asayama T, Imai T. Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions. Clinical Neuropathology. 15: 41-6. PMID 8998856 |
0.32 |
|
| 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 |
0.573 |
|
| 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 |
0.642 |
|
| 1996 |
Oka N, Kusaka H, Kusunoki S, Tsuda H, Kaji R, Imai T, Akiguchi I, Kimura J. IgM M-protein with antibody activity against gangliosides with disialosyl residue in sensory neuropathy binds to sensory neurons. Muscle & Nerve. 19: 528-0. PMID 8622736 DOI: 10.1002/(Sici)1097-4598(199604)19:4<528::Aid-Mus15>3.0.Co;2-L |
0.468 |
|
| 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 |
0.567 |
|
| 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 |
0.607 |
|
| 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 |
0.716 |
|
| 1993 |
Matsumoto S, Goto S, Kusaka H, Imai T, Murakami N, Hashizume Y, Okazaki H, Hirano A. Ubiquitin-positive inclusion in anterior horn cells in subgroups of motor neuron diseases: a comparative study of adult-onset amyotrophic lateral sclerosis, juvenile amyotrophic lateral sclerosis and Werdnig-Hoffmann disease. Journal of the Neurological Sciences. 115: 208-13. PMID 8387100 DOI: 10.1016/0022-510X(93)90226-O |
0.811 |
|
| 1993 |
Matsumoto S, Kusaka H, Ito H, Yamasaki M, Imai T. [A comparative immunohistochemical study of ubiquitin-positive skein-like inclusions in anterior horn neurons in subgroups of adult-onset motor neuron diseases]. Rinshå Shinkeigaku = Clinical Neurology. 33: 1125-30. PMID 8124868 |
0.306 |
|
| 1992 |
Matsumoto S, Kusaka H, Murakami N, Hashizume Y, Okazaki H, Hirano A. Basophilic inclusions in sporadic juvenile amyotrophic lateral sclerosis: an immunocytochemical and ultrastructural study. Acta Neuropathologica. 83: 579-83. PMID 1636375 DOI: 10.1007/Bf00299405 |
0.744 |
|
| 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 |
0.447 |
|
| 1992 |
Okamoto K, Murakami N, Kusaka H, Yoshida M, Hashizume Y, Nakazato Y, Matsubara E, Hirai S. Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease. Journal of Neurology. 239: 426-30. PMID 1333007 DOI: 10.1007/Bf00856806 |
0.687 |
|
| 1990 |
Kusaka H, Matsumoto S, Imai T. An adult-onset case of sporadic motor neuron disease with basophilic inclusions. Acta Neuropathologica. 80: 660-5. PMID 1703386 DOI: 10.1007/Bf00307636 |
0.386 |
|
| 1988 |
Kusaka H, Imai T, Hashimoto S, Yamamoto T, Maya K, Yamasaki M. Ultrastructural study of chromatolytic neurons in an adult-onset sporadic case of amyotrophic lateral sclerosis. Acta Neuropathologica. 75: 523-8. PMID 3376756 DOI: 10.1007/BF00687142 |
0.719 |
|
| 1986 |
Kusaka H, Hirano A, Bornstein MB, Moore GR, Raine CS. Transformation of cells of astrocyte lineage into macrophage-like cells in organotypic cultures of mouse spinal cord tissue. Journal of the Neurological Sciences. 72: 77-89. PMID 2419515 DOI: 10.1016/0022-510X(86)90037-7 |
0.451 |
|
| 1985 |
Kubota T, Kusaka H, Hirano A, Llena J. Ultrastructural study of early stage of calcification in herpes simplex encephalitis. Acta Neuropathologica. 68: 77-9. PMID 4050355 DOI: 10.1007/Bf00688960 |
0.564 |
|
| 1985 |
Kusaka H, Hirano A. Fine structure of anterior horns in patients without amyotrophic lateral sclerosis. Journal of Neuropathology and Experimental Neurology. 44: 430-8. PMID 4040157 DOI: 10.1097/00005072-198507000-00006 |
0.52 |
|
| 1985 |
Kusaka H, Hirano A, Bornstein MB, Raine CS. Fine structure of astrocytic processes during serum-induced demyelination in vitro. Journal of the Neurological Sciences. 69: 255-67. PMID 4031946 DOI: 10.1016/0022-510X(85)90138-8 |
0.438 |
|
| 1985 |
Kusaka H, Hirano A, Bornstein MB, Raine CS. Basal lamina formation by astrocytes in organotypic cultures of mouse spinal cord tissue. Journal of Neuropathology and Experimental Neurology. 44: 295-303. PMID 3989584 DOI: 10.1097/00005072-198505000-00007 |
0.445 |
|
| 1984 |
Kusaka H, Hirano A, Bornstein MB, Raine CS. The organization of astrocytes in organotypic mouse spinal cord culture: an electron microscope study. Neuropathology and Applied Neurobiology. 10: 411-22. PMID 6527730 DOI: 10.1111/J.1365-2990.1984.Tb00390.X |
0.468 |
|
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