| Year |
Citation |
Score |
| 2023 |
Ohira M, Yoshii K, Aso Y, Nakajima H, Yamashita T, Takahashi-Iwata I, Maeda N, Shindo K, Suenaga T, Matsuura T, Sugie K, Hamano T, Arai A, Furutani R, Suzuki Y, ... ... Mizusawa H, et al. First evidence of tick-borne encephalitis (TBE) outside of Hokkaido Island in Japan. Emerging Microbes & Infections. 12: 2278898. PMID 37906509 DOI: 10.1080/22221751.2023.2278898 |
0.424 |
|
| 2023 |
Nakahara Y, Mitsui J, Date H, Porto KJ, Hayashi Y, Yamashita A, Kusakabe Y, Matsukawa T, Ishiura H, Yasuda T, Iwata A, Goto J, Ichikawa Y, Momose Y, Takahashi Y, ... ... Mizusawa H, et al. Genome-wide association study identifies a new susceptibility locus in for Multiple System Atrophy. Medrxiv : the Preprint Server For Health Sciences. PMID 37425910 DOI: 10.1101/2023.05.02.23289328 |
0.385 |
|
| 2019 |
Takeuchi A, Mohri S, Kai H, Tamaoka A, Kobayashi A, Mizusawa H, Iwasaki Y, Yoshida M, Shimizu H, Murayama S, Kuroda S, Morita M, Parchi P, Kitamoto T. Two distinct prions in fatal familial insomnia and its sporadic form. Brain Communications. 1: fcz045. PMID 32954274 DOI: 10.1093/braincomms/fcz045 |
0.49 |
|
| 2015 |
Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, ... ... Mizusawa H, et al. Variants associated with Gaucher disease in multiple system atrophy. Annals of Clinical and Translational Neurology. 2: 417-26. PMID 25909086 DOI: 10.1002/Acn3.185 |
0.437 |
|
| 2013 |
Kobayashi Z, Kawakami I, Arai T, Yokota O, Tsuchiya K, Kondo H, Shimomura Y, Haga C, Aoki N, Hasegawa M, Hosokawa M, Oshima K, Niizato K, Ishizu H, Terada S, ... ... Mizusawa H, et al. Pathological features of FTLD-FUS in a Japanese population: analyses of nine cases. Journal of the Neurological Sciences. 335: 89-95. PMID 24050818 DOI: 10.1016/J.Jns.2013.08.035 |
0.463 |
|
| 2013 |
Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Iwata A, Goto J, Yamamoto Y, Komata M, Shirahige K, ... ... Mizusawa H, et al. Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration New England Journal of Medicine. 369: 233-244. PMID 23758206 DOI: 10.1056/Nejmoa1212115 |
0.454 |
|
| 2013 |
Takahashi M, Obayashi M, Ishiguro T, Sato N, Niimi Y, Ozaki K, Mogushi K, Mahmut Y, Tanaka H, Tsuruta F, Dolmetsch R, Yamada M, Takahashi H, Kato T, Mori O, ... ... Mizusawa H, et al. Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death. Plos One. 8: e50121. PMID 23505410 DOI: 10.1371/Journal.Pone.0050121 |
0.434 |
|
| 2012 |
Suzuki F, Kubota T, Miyazaki Y, Ishikawa K, Ebisawa M, Hirohata S, Ogura T, Mizusawa H, Imai T, Miyasaka N, Nanki T. Serum level of soluble CX3CL1/fractalkine is elevated in patients with polymyositis and dermatomyositis, which is correlated with disease activity. Arthritis Research & Therapy. 14: R48. PMID 22394569 DOI: 10.1186/ar3761 |
0.38 |
|
| 2012 |
Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama S, Mori O, Eishi Y, Mizusawa H. Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 32: 595-603. PMID 22393909 DOI: 10.1111/J.1440-1789.2012.01302.X |
0.434 |
|
| 2012 |
Uchida A, Sasaguri H, Kimura N, Tajiri M, Ohkubo T, Ono F, Sakaue F, Kanai K, Hirai T, Sano T, Shibuya K, Kobayashi M, Yamamoto M, Yokota S, Kubodera T, ... ... Mizusawa H, et al. Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43. Brain : a Journal of Neurology. 135: 833-46. PMID 22252998 DOI: 10.1093/brain/awr348 |
0.417 |
|
| 2011 |
Yamane J, Ishibashi S, Sakaguchi M, Kuroiwa T, Kanemura Y, Nakamura M, Miyoshi H, Sawamoto K, Toyama Y, Mizusawa H, Okano H. Transplantation of human neural stem/progenitor cells overexpressing galectin-1 improves functional recovery from focal brain ischemia in the Mongolian gerbil. Molecular Brain. 4: 35. PMID 21951913 DOI: 10.1186/1756-6606-4-35 |
0.4 |
|
| 2011 |
Kobayashi Z, Tsuchiya K, Kubodera T, Shibata N, Arai T, Miura H, Ishikawa C, Kondo H, Ishizu H, Akiyama H, Mizusawa H. FALS with Gly72Ser mutation in SOD1 gene: report of a family including the first autopsy case. Journal of the Neurological Sciences. 300: 9-13. PMID 21084099 DOI: 10.1016/J.Jns.2010.10.030 |
0.446 |
|
| 2010 |
Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, et al. Prospective 10-year surveillance of human prion diseases in Japan. Brain : a Journal of Neurology. 133: 3043-57. PMID 20855418 DOI: 10.1093/Brain/Awq216 |
0.508 |
|
| 2010 |
Katsuno M, Banno H, Suzuki K, Takeuchi Y, Kawashima M, Yabe I, Sasaki H, Aoki M, Morita M, Nakano I, Kanai K, Ito S, Ishikawa K, Mizusawa H, Yamamoto T, et al. Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial. The Lancet. Neurology. 9: 875-84. PMID 20691641 DOI: 10.1016/S1474-4422(10)70182-4 |
0.374 |
|
| 2010 |
Nanri K, Koizumi K, Mitoma H, Taguchi T, Takeguchi M, Ishiko T, Otsuka T, Nishioka H, Mizusawa H. Classification of cerebellar atrophy using voxel-based morphometry and SPECT with an easy Z-score imaging system. Internal Medicine (Tokyo, Japan). 49: 535-41. PMID 20228587 DOI: 10.2169/Internalmedicine.49.2785 |
0.437 |
|
| 2010 |
Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, ... ... Mizusawa H, et al. The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells. Acta Neuropathologica. 119: 447-64. PMID 20043227 DOI: 10.1007/S00401-009-0630-0 |
0.54 |
|
| 2009 |
Sato N, Amino T, Kobayashi K, Asakawa S, Ishiguro T, Tsunemi T, Takahashi M, Matsuura T, Flanigan KM, Iwasaki S, Ishino F, Saito Y, Murayama S, Yoshida M, Hashizume Y, ... ... Mizusawa H, et al. Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n. American Journal of Human Genetics. 85: 544-57. PMID 19878914 DOI: 10.1016/J.Ajhg.2009.09.019 |
0.462 |
|
| 2009 |
Miki K, Ishibashi S, Sun L, Xu H, Ohashi W, Kuroiwa T, Mizusawa H. Intensity of chronic cerebral hypoperfusion determines white/gray matter injury and cognitive/motor dysfunction in mice. Journal of Neuroscience Research. 87: 1270-81. PMID 18951530 DOI: 10.1002/jnr.21925 |
0.422 |
|
| 2009 |
Sun L, Kuroiwa T, Ishibashi S, Miki K, Li S, Xu H, Endo S, Mizusawa H. Two region-dependent pathways of eosinophilic neuronal death after transient cerebral ischemia. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 29: 45-54. PMID 18627483 DOI: 10.1111/j.1440-1789.2008.00939.x |
0.441 |
|
| 2007 |
Shiga Y, Satoh K, Kitamoto T, Kanno S, Nakashima I, Sato S, Fujihara K, Takata H, Nobukuni K, Kuroda S, Takano H, Umeda Y, Konno H, Nagasato K, Satoh A, ... ... Mizusawa H, et al. Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution. Journal of Neurology. 254: 1509-17. PMID 17965961 DOI: 10.1007/S00415-007-0540-9 |
0.502 |
|
| 2007 |
Ishibashi S, Kuroiwa T, Sakaguchi M, Sun L, Kadoya T, Okano H, Mizusawa H. Galectin-1 regulates neurogenesis in the subventricular zone and promotes functional recovery after stroke. Experimental Neurology. 207: 302-13. PMID 17706645 DOI: 10.1016/J.Expneurol.2007.06.024 |
0.421 |
|
| 2006 |
Ishibashi S, Kuroiwa T, LiYuan S, Katsumata N, Li S, Endo S, Mizusawa H. Long-term cognitive and neuropsychological symptoms after global cerebral ischemia in Mongolian gerbils. Acta Neurochirurgica. Supplement. 96: 299-302. PMID 16671475 |
0.405 |
|
| 2006 |
Sun L, Kuroiwa T, Ishibashi S, Katsumata N, Endo S, Mizusawa H. Time profile of eosinophilic neurons in the cortical layers and cortical atrophy. Acta Neurochirurgica. Supplement. 96: 272-5. PMID 16671469 |
0.409 |
|
| 2006 |
Uchihara T, Takeda Y, Kobayashi T, Kasuga T, Ishikawa K, Kirei K, Mizusawa H, Endo T, Hirokawa K, Kuroiwa T. Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene. Journal of Neurology. 253: 396-8. PMID 16311891 DOI: 10.1007/s00415-005-0980-z |
0.383 |
|
| 2006 |
Sun L, Kuroiwa T, Ishibashi S, Katsumata N, Endo S, Mizusawa H. Transition of areas of eosinophilic neurons and reactive astrocytes to delayed cortical infarcts after transient unilateral forebrain ischemia in Mongolian gerbils. Acta Neuropathologica. 111: 21-8. PMID 16311772 DOI: 10.1007/s00401-005-1081-x |
0.403 |
|
| 2005 |
Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, ... ... Mizusawa H, et al. An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains. American Journal of Human Genetics. 77: 280-96. PMID 16001362 DOI: 10.1086/432518 |
0.437 |
|
| 2005 |
Hamaguchi T, Kitamoto T, Sato T, Mizusawa H, Nakamura Y, Noguchi M, Furukawa Y, Ishida C, Kuji I, Mitani K, Murayama S, Kohriyama T, Katayama S, Yamashita M, Yamamoto T, et al. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease. Neurology. 64: 643-8. PMID 15728285 DOI: 10.1212/01.Wnl.0000151847.57956.Fa |
0.505 |
|
| 2004 |
Ishibashi S, Sakaguchi M, Kuroiwa T, Yamasaki M, Kanemura Y, Shizuko I, Shimazaki T, Onodera M, Okano H, Mizusawa H. Human neural stem/progenitor cells, expanded in long-term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils. Journal of Neuroscience Research. 78: 215-23. PMID 15378509 DOI: 10.1002/Jnr.20246 |
0.421 |
|
| 2004 |
Takahashi H, Ishikawa K, Tsutsumi T, Fujigasaki H, Kawata A, Okiyama R, Fujita T, Yoshizawa K, Yamaguchi S, Tomiyasu H, Yoshii F, Mitani K, Shimizu N, Yamazaki M, Miyamoto T, ... ... Mizusawa H, et al. A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6. Journal of Human Genetics. 49: 256-64. PMID 15362569 DOI: 10.1007/S10038-004-0142-7 |
0.52 |
|
| 2004 |
Ishibashi S, Kuroiwa T, Katsumata N, Yuan SL, Endo S, Mizusawa H. Extrapyramidal motor symptoms versus striatal infarction volume after focal ischemia in mongolian gerbils. Neuroscience. 127: 269-75. PMID 15262318 DOI: 10.1016/j.neuroscience.2004.04.039 |
0.433 |
|
| 2003 |
Ishibashi S, Kuroiwa T, Endo S, Okeda R, Mizusawa H. Neurological dysfunctions versus regional infarction volume after focal ischemia in Mongolian gerbils. Stroke; a Journal of Cerebral Circulation. 34: 1501-6. PMID 12750539 DOI: 10.1161/01.STR.0000074034.32371.13 |
0.418 |
|
| 2002 |
Zhao F, Kuroiwa T, Miyasaka N, Nagaoka T, Nakane M, Tamura A, Mizusawa H. Ultrastructural and MRI study of the substantia nigra evolving exofocal post-ischemic neuronal death in the rat. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 22: 91-105. PMID 12416550 DOI: 10.1046/j.1440-1789.2002.00437.x |
0.422 |
|
| 2002 |
Arai A, Tanaka K, Ikeuchi T, Igarashi S, Kobayashi H, Asaka T, Date H, Saito M, Tanaka H, Kawasaki S, Uyama E, Mizusawa H, Fukuhara N, Tsuji S. A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees. Annals of Neurology. 52: 516-9. PMID 12325084 DOI: 10.1002/Ana.10341 |
0.53 |
|
| 2001 |
Takenoshita H, Shizuka-Ikeda M, Mitoma H, Song S, Harigaya Y, Igeta Y, Yaguchi M, Ishida K, Shoji M, Tanaka M, Mizusawa H, Okamoto K. Presynaptic inhibition of cerebellar GABAergic transmission by glutamate decarboxylase autoantibodies in progressive cerebellar ataxia. Journal of Neurology, Neurosurgery, and Psychiatry. 70: 386-9. PMID 11181864 DOI: 10.1136/Jnnp.70.3.386 |
0.395 |
|
| 1992 |
Mochizuki A, Mizusawa H, Ohkoshi N, Yoshizawa K, Komatsuzaki Y, Inoue K, Kanazawa I. Argentophilic intracytoplasmic inclusions in multiple system atrophy. Journal of Neurology. 239: 311-6. PMID 1380981 DOI: 10.1007/BF00867586 |
0.577 |
|
| 1991 |
Mizusawa H, Nakamura H, Wakayama I, Yen SH, Hirano A. Skein-like inclusions in the anterior horn cells in motor neuron disease. Journal of the Neurological Sciences. 105: 14-21. PMID 1665504 DOI: 10.1016/0022-510X(91)90112-K |
0.562 |
|
| 1989 |
Mizusawa H, Yen SH, Hirano A, Llena JF. Pathology of the dentate nucleus in progressive supranuclear palsy: a histological, immunohistochemical and ultrastructural study. Acta Neuropathologica. 78: 419-28. PMID 2782052 DOI: 10.1007/Bf00688179 |
0.475 |
|
| 1989 |
Mizusawa H, Matsumoto S, Yen SH, Hirano A, Rojas-Corona RR, Donnenfeld H. Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis. Acta Neuropathologica. 79: 37-43. PMID 2511732 DOI: 10.1007/Bf00308955 |
0.457 |
|
| 1988 |
Mizusawa H, Hirano A, Llena F. Nuclear bridges within multinucleated giant cells in subacute encephalitis of acquired immune deficiency syndrome (AIDS). Acta Neuropathologica. 76: 166-9. PMID 3407394 DOI: 10.1007/Bf00688100 |
0.442 |
|
| 1988 |
Mizusawa H, Hirano A, Llena JF, Shintaku M. Cerebrovascular lesions in acquired immune deficiency syndrome (AIDS). Acta Neuropathologica. 76: 451-7. PMID 3188838 DOI: 10.1007/Bf00686383 |
0.601 |
|
| 1987 |
Mizusawa H, Kurisaki H, Takatsu M, Inoue K, Mannen T, Toyokura Y, Nakanishi T. Rimmed vacuolar distal myopathy: a clinical, electrophysiological, histopathological and computed tomographic study of seven cases. Journal of Neurology. 234: 129-36. PMID 3585419 DOI: 10.1007/BF00314131 |
0.494 |
|
| 1987 |
Mizusawa H, Hirano A, Llena JF, Kato T. Nuclear bridges in multinucleated giant cells associated with primary lymphoma of the brain in acquired immune deficiency syndrome (AIDS). Acta Neuropathologica. 75: 23-6. PMID 3434211 DOI: 10.1007/Bf00686788 |
0.448 |
|
| 1987 |
Mizusawa H, Hirano A, Llena JF. Involvement of hippocampus in Creutzfeldt-Jakob disease. Journal of the Neurological Sciences. 82: 13-26. PMID 3326910 DOI: 10.1016/0022-510X(87)90003-7 |
0.479 |
|
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