| Clinicopathological features of adult-onset neuronal intranuclear inclusion disease J Sone, K Mori, T Inagaki, R Katsumata, S Takagi, S Yokoi, K Araki, T Kato, ... Brain 139 (12), 3170-3186, 2016 | 320 | 2016 |
| Autosomal dominant Parkinson's disease caused by SNCA duplications T Konno, OA Ross, A Puschmann, DW Dickson, ZK Wszolek Parkinsonism & related disorders 22, S1-S6, 2016 | 185 | 2016 |
| CSF1R-related leukoencephalopathy: A major player in primary microgliopathies T Konno, K Kasanuki, T Ikeuchi, DW Dickson, ZK Wszolek Neurology 91 (24), 1092-1104, 2018 | 152 | 2018 |
| A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ... Journal of medical genetics 51 (6), 419-424, 2014 | 146 | 2014 |
| Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation T Konno, K Yoshida, T Mizuno, T Kawarai, M Tada, H Nozaki, SI Ikeda, ... European Journal of Neurology 24 (1), 37-45, 2017 | 140 | 2017 |
| Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS T Konno, M Tada, M Tada, A Koyama, H Nozaki, Y Harigaya, J Nishimiya, ... Neurology 82 (2), 139-148, 2014 | 125 | 2014 |
| Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43 A Koyama, A Sugai, T Kato, T Ishihara, A Shiga, Y Toyoshima, M Koyama, ... Nucleic acids research 44 (12), 5820-5836, 2016 | 102 | 2016 |
| Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72 T Konno, A Shiga, A Tsujino, A Sugai, T Kato, K Kanai, A Yokoseki, ... Journal of Neurology, Neurosurgery & Psychiatry 84 (4), 398-401, 2013 | 92 | 2013 |
| DCTN1-related neurodegeneration: Perry syndrome and beyond T Konno, OA Ross, HAG Teive, J Sławek, DW Dickson, ZK Wszolek Parkinsonism & related disorders 41, 14-24, 2017 | 81 | 2017 |
| Diagnostic Criteria for Adult‐onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia Due to CSF1R mutation T Konno, K Yoshida, I Mizuta, T Mizuno, T Kawarai, M Tada, H Nozaki, ... European Journal of Neurology, 2017 | 75 | 2017 |
| Diagnostic value of brain calcifications in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia T Konno, DF Broderick, N Mezaki, A Isami, D Kaneda, Y Tashiro, ... American Journal of Neuroradiology 38 (1), 77-83, 2017 | 59 | 2017 |
| Hypertrophic olivary degeneration: a clinico-radiologic study T Konno, DF Broderick, P Tacik, JN Caviness, ZK Wszolek Parkinsonism & related disorders 28, 36-40, 2016 | 58 | 2016 |
| Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: evidence for clinico-pathologic subtypes R Takeuchi, M Tada, A Shiga, Y Toyoshima, T Konno, T Sato, H Nozaki, ... Acta neuropathologica communications 4, 1-13, 2016 | 53 | 2016 |
| Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids M Tada, T Konno, M Tada, T Tezuka, T Miura, N Mezaki, K Okazaki, ... Annals of Neurology 80 (4), 554-565, 2016 | 53 | 2016 |
| Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with an SLC20A2 mutation T Kimura, T Miura, K Aoki, S Saito, H Hondo, T Konno, A Uchiyama, ... Neuropathology 36 (4), 365-371, 2016 | 47 | 2016 |
| Comparison of clinical features among Parkinson's disease subtypes: a large retrospective study in a single center T Konno, A Deutschländer, MG Heckman, M Ossi, ER Vargas, ... Journal of the neurological sciences 386, 39-45, 2018 | 45 | 2018 |
| Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia: review of clinical manifestations as foundations for therapeutic development S Papapetropoulos, A Pontius, E Finger, V Karrenbauer, DS Lynch, ... Frontiers in neurology 12, 788168, 2022 | 40 | 2022 |
| Diffuse Lewy body disease manifesting as corticobasal syndrome: a rare form of Lewy body disease K Kasanuki, KA Josephs, TJ Ferman, ME Murray, S Koga, T Konno, ... Neurology 91 (3), e268-e279, 2018 | 40 | 2018 |
| Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3 M Prudencio, H Garcia-Moreno, KR Jansen-West, RH Al-Shaikh, ... Science translational medicine 12 (566), eabb7086, 2020 | 37 | 2020 |
| Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease A Sasaki, A Kakita, K Yoshida, T Konno, T Ikeuchi, S Hayashi, H Matsuo, ... Neurogenetics 16, 265-276, 2015 | 37 | 2015 |
Osamu OnoderaDept. of Neurology, Brain Research Institute, Niigata University在 bri.niigata-u.ac.jp 的电子邮件经过验证
