| Year |
Citation |
Score |
| 2024 |
Walton RL, Koga S, Beasley AI, White LJ, Griesacker T, Murray ME, Kasanuki K, Hou X, Fiesel FC, Springer W, Uitti RJ, Fields JA, Botha H, Ramanan VK, Kantarci K, et al. Role of GBA variants in Lewy body disease neuropathology. Acta Neuropathologica. 147: 54. PMID 38472443 DOI: 10.1007/s00401-024-02699-w |
0.34 |
|
| 2023 |
Carlos AF, Sekiya H, Koga S, Gatto RG, Casey MC, Pham NTT, Sintini I, Machulda MM, Jack CR, Lowe VJ, Whitwell JL, Petrucelli L, Reichard RR, Petersen RC, Dickson DW, et al. Clinicopathologic features of a novel star-shaped transactive response DNA-binding protein 43 (TDP-43) pathology in the oldest old. Journal of Neuropathology and Experimental Neurology. PMID 38086178 DOI: 10.1093/jnen/nlad105 |
0.302 |
|
| 2023 |
Hou X, Heckman MG, Fiesel FC, Koga S, Soto-Beasley AI, Watzlawik JO, Zhao J, Valentino RR, Johnson PW, White LJ, Quicksall ZS, Reddy JS, Bras J, Guerreiro R, Zhao N, et al. Genome-wide association study identifies and variants as mitophagy modifiers in Lewy body disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37905059 DOI: 10.1101/2023.10.16.23297100 |
0.303 |
|
| 2023 |
Carlos AF, Koga S, Graff-Radford NR, Baker MC, Rademakers R, Ross OA, Dickson DW, Josephs KA. Senile plaque-associated transactive response DNA-binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 37525358 DOI: 10.1111/neup.12938 |
0.355 |
|
| 2023 |
Koga S, Murakami A, Soto-Beasley AI, Walton RL, Baker MC, Castanedes-Casey M, Josephs KA, Ross OA, Dickson DW. Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies. Acta Neuropathologica Communications. 11: 109. PMID 37415197 DOI: 10.1186/s40478-023-01611-z |
0.305 |
|
| 2023 |
Shir D, Thu Pham NT, Botha H, Koga S, Kouri N, Ali F, Knopman DS, Petersen RC, Boeve BF, Kremers WK, Nguyen AT, Murray ME, Reichard RR, Dickson DW, Graff-Radford N, et al. Clinicoradiologic and Neuropathologic Evaluation of Corticobasal Syndrome. Neurology. PMID 37268436 DOI: 10.1212/WNL.0000000000207397 |
0.657 |
|
| 2023 |
Tunold JA, Tan MMX, Koga S, Geut H, Rozemuller AJM, Valentino R, Sekiya H, Martin NB, Heckman MG, Bras J, Guerreiro R, Dickson DW, Toft M, van de Berg W, Ross OA, et al. Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease. Brain : a Journal of Neurology. PMID 37247383 DOI: 10.1093/brain/awad183 |
0.368 |
|
| 2023 |
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, ... ... Koga S, et al. Creating the Pick's disease International Consortium: Association study of H2 haplotype with risk of Pick's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37163045 DOI: 10.1101/2023.04.17.23288471 |
0.357 |
|
| 2023 |
Martin NB, Koga S, Appleby BS, Sekiya H, Dickson D. Creutzfeldt-Jakob Disease Misdiagnosed as Multiple System Atrophy. Movement Disorders Clinical Practice. 10: 496-500. PMID 36949796 DOI: 10.1002/mdc3.13654 |
0.305 |
|
| 2022 |
Koga S, Ali S, Baker MC, Wierenga KJ, Dompenciel M, Dickson DW, Wszolek ZK. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia? Parkinsonism & Related Disorders. PMID 36396537 DOI: 10.1016/j.parkreldis.2022.11.008 |
0.319 |
|
| 2022 |
Hopfner F, Tietz AK, Ruf VC, Ross OA, Koga S, Dickson D, Aguzzi A, Attems J, Beach T, Beller A, Cheshire WP, van Deerlin V, Desplats P, Deuschl G, Duyckaerts C, et al. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 35997131 DOI: 10.1002/mds.29164 |
0.332 |
|
| 2022 |
Valentino RR, Ramnarine C, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Kasanuki K, Murray ME, Uitti RJ, Fields JA, Botha H, Ramanan VK, Kantarci K, Lowe VJ, et al. Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures. Acta Neuropathologica Communications. 10: 103. PMID 35836284 DOI: 10.1186/s40478-022-01399-4 |
0.319 |
|
| 2022 |
Koga S, Josephs KA, Aiba I, Yoshida M, Dickson DW. Neuropathology and emerging biomarkers in corticobasal syndrome. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 35697501 DOI: 10.1136/jnnp-2021-328586 |
0.376 |
|
| 2022 |
Koga S, Aiba I. [Autonomic Dysfunction in Tauopathies]. Brain and Nerve = Shinkei Kenkyu No Shinpo. 74: 257-262. PMID 35260524 DOI: 10.11477/mf.1416202021 |
0.305 |
|
| 2022 |
Koga S, Murakami A, Josephs KA, Dickson DW. Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 35029300 DOI: 10.1111/neup.12780 |
0.349 |
|
| 2021 |
Meneses A, Koga S, O'Leary J, Dickson DW, Bu G, Zhao N. TDP-43 Pathology in Alzheimer's Disease. Molecular Neurodegeneration. 16: 84. PMID 34930382 DOI: 10.1186/s13024-021-00503-x |
0.323 |
|
| 2021 |
Koga S, Sekiya H, Kondru N, Ross OA, Dickson DW. Neuropathology and molecular diagnosis of Synucleinopathies. Molecular Neurodegeneration. 16: 83. PMID 34922583 DOI: 10.1186/s13024-021-00501-z |
0.315 |
|
| 2021 |
Koga S, Zhou X, Murakami A, Castro CF, Baker MC, Rademakers R, Dickson DW. Concurrent tau pathologies in frontotemporal lobar degeneration with TDP-43 pathology. Neuropathology and Applied Neurobiology. PMID 34823271 DOI: 10.1111/nan.12778 |
0.337 |
|
| 2020 |
Valentino RR, Koga S, Walton RL, Soto-Beasley AI, Kouri N, DeTure MA, Murray ME, Johnson PW, Petersen RC, Boeve BF, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA, Heckman MG. MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features. Acta Neuropathologica Communications. 8: 218. PMID 33287913 DOI: 10.1186/s40478-020-01097-z |
0.726 |
|
| 2020 |
Valentino RR, Tamvaka N, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA. Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures. Acta Neuropathologica Communications. 8: 162. PMID 32943110 DOI: 10.1186/S40478-020-01035-Z |
0.449 |
|
| 2020 |
Koga S, Dickson DW, Wszolek ZK. Letter to the editor, "Movement disorders rounds: A case of missing pathology in a patient with LRRK2 Parkinson's disease". Parkinsonism & Related Disorders. PMID 32921567 DOI: 10.1016/J.Parkreldis.2020.08.036 |
0.409 |
|
| 2020 |
Prudencio M, Humphrey J, Pickles S, Brown AL, Hill SE, Kachergus J, Shi J, Heckman M, Spiegel M, Cook C, Song Y, Yue M, Daughrity L, Carlomagno Y, Jansen-West K, ... ... Koga S, et al. Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. The Journal of Clinical Investigation. PMID 32790644 DOI: 10.1172/Jci139741 |
0.469 |
|
| 2020 |
Zhou X, Brooks M, Jiang P, Koga S, Zuberi AR, Baker MC, Parsons TM, Castanedes-Casey M, Phillips V, Librero AL, Kurti A, Fryer JD, Bu G, Lutz C, Dickson DW, et al. Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin-deficient mice. Embo Reports. e50197. PMID 32761777 DOI: 10.15252/Embr.202050197 |
0.363 |
|
| 2020 |
Wernick AI, Walton RL, Koga S, Soto-Beasley AI, Heckman MG, Gan-Or Z, Ren Y, Rademakers R, Uitti RJ, Wszolek ZK, Cheshire WP, Dickson DW, Ross OA. GBA variation and susceptibility to multiple system atrophy. Parkinsonism & Related Disorders. 77: 64-69. PMID 32623306 DOI: 10.1016/J.Parkreldis.2020.06.007 |
0.441 |
|
| 2020 |
Koga S, Roemer SF, Tipton PW, Low PA, Josephs KA, Dickson DW. Cerebrovascular pathology and misdiagnosis of multiple system atrophy: An autopsy study. Parkinsonism & Related Disorders. 75: 34-40. PMID 32450546 DOI: 10.1016/J.Parkreldis.2020.05.018 |
0.441 |
|
| 2020 |
Koga S, Li F, Zhao N, Roemer SF, Ferman TJ, Wernick AI, Walton RL, Faroqi AH, Graff-Radford NR, Cheshire WP, Ross OA, Dickson DW. Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease. Brain Pathology (Zurich, Switzerland). PMID 32232888 DOI: 10.1111/Bpa.12839 |
0.461 |
|
| 2020 |
Valentino RR, Koga S, Heckman MG, Brushaber DE, Diehl NN, Walton RL, Dickson DW, Ross OA. Association of Tripartite Motif Containing 11 rs564309 with Tau Pathology in Progressive Supranuclear Palsy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32142177 DOI: 10.1002/Mds.28010 |
0.41 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31748840 DOI: 10.1007/S00401-019-02092-Y |
0.359 |
|
| 2019 |
Koga S, Roemer SF, Kasanuki K, Dickson DW. Cerebrovascular pathology presenting as corticobasal syndrome: An autopsy case series of "vascular CBS". Parkinsonism & Related Disorders. 68: 79-84. PMID 31621626 DOI: 10.1016/J.Parkreldis.2019.09.001 |
0.4 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31616982 DOI: 10.1007/S00401-019-02080-2 |
0.417 |
|
| 2019 |
Takahata K, Kimura Y, Sahara N, Koga S, Shimada H, Ichise M, Saito F, Moriguchi S, Kitamura S, Kubota M, Umeda S, Niwa F, Mizushima J, Morimoto Y, Funayama M, et al. PET-detectable tau pathology correlates with long-term neuropsychiatric outcomes in patients with traumatic brain injury. Brain : a Journal of Neurology. PMID 31504227 DOI: 10.1093/Brain/Awz238 |
0.672 |
|
| 2019 |
Heckman MG, Kasanuki K, Brennan RR, Labbé C, Vargas ER, Soto AI, Murray ME, Koga S, Dickson DW, Ross OA. Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 31234228 DOI: 10.1002/Mds.27773 |
0.625 |
|
| 2019 |
Koga S, Eric Ahlskog J, DeTure MA, Baker M, Roemer SF, Konno T, Rademakers R, Ross OA, Dickson DW. Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1. Journal of Neuropathology and Experimental Neurology. PMID 31216016 DOI: 10.1093/Jnen/Nlz048 |
0.462 |
|
| 2019 |
Endo H, Shimada H, Sahara N, Ono M, Koga S, Kitamura S, Niwa F, Hirano S, Kimura Y, Ichise M, Shinotoh H, Zhang MR, Kuwabara S, Dickson DW, Toda T, et al. In vivo binding of a tau imaging probe, [ C]PBB3, in patients with progressive supranuclear palsy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 30892739 DOI: 10.1002/Mds.27643 |
0.532 |
|
| 2019 |
Heckman MG, Brennan RR, Labbé C, Soto AI, Koga S, DeTure MA, Murray ME, Petersen RC, Boeve BF, van Gerpen JA, Uitti RJ, Wszolek ZK, Rademakers R, Dickson DW, Ross OA. Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology. Jama Neurology. PMID 30882841 DOI: 10.1001/Jamaneurol.2019.0250 |
0.625 |
|
| 2019 |
Kasanuki K, Koga S, Dickson DW, Sato K, Iseki E, Ichimiya Y, Arai H. Mixed Alzheimer's and Lewy-related Pathology Can Cause Corticobasal Syndrome with Visual Hallucinations. Internal Medicine (Tokyo, Japan). PMID 30799336 DOI: 10.2169/Internalmedicine.1427-18 |
0.445 |
|
| 2018 |
Zhao N, Liu CC, Van Ingelgom AJ, Linares C, Kurti A, Knight JA, Heckman MG, Diehl NN, Shinohara M, Martens YA, Attrebi ON, Petrucelli L, Fryer JD, Wszolek ZK, Graff-Radford NR, ... ... Koga S, et al. APOE ε2 is associated with increased tau pathology in primary tauopathy. Nature Communications. 9: 4388. PMID 30348994 DOI: 10.1038/S41467-018-06783-0 |
0.628 |
|
| 2018 |
Liesinger AM, Graff-Radford NR, Duara R, Carter RE, Hanna Al-Shaikh FS, Koga S, Hinkle KM, DiLello SK, Johnson MF, Aziz A, Ertekin-Taner N, Ross OA, Dickson DW, Murray ME. Sex and age interact to determine clinicopathologic differences in Alzheimer's disease. Acta Neuropathologica. PMID 30219939 DOI: 10.1007/S00401-018-1908-X |
0.539 |
|
| 2018 |
Allen M, Wang X, Serie DJ, Strickland SL, Burgess JD, Koga S, Younkin CS, Nguyen TT, Malphrus KG, Lincoln SJ, Alamprese M, Zhu K, Chang R, Carrasquillo MM, Kouri N, et al. Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy. Acta Neuropathologica. PMID 30136084 DOI: 10.1007/S00401-018-1900-5 |
0.725 |
|
| 2018 |
Koga S, Dickson DW. "Minimal change" multiple system atrophy with limbic-predominant α-synuclein pathology. Acta Neuropathologica. PMID 30128820 DOI: 10.1007/S00401-018-1901-4 |
0.341 |
|
| 2018 |
Ogaki K, Heckman MG, Koga S, Martens YA, Labbé C, Lorenzo-Betancor O, Walton RL, Soto AI, Vargas ER, Fujioka S, Uitti RJ, van Gerpen JA, Cheshire WP, Younkin SG, Wszolek ZK, et al. Association study between multiple system atrophy and TREM2 p.R47H. Neurology. Genetics. 4: e257. PMID 30109269 DOI: 10.1212/Nxg.0000000000000257 |
0.404 |
|
| 2018 |
Koga S, Kouri N, Walton RL, Ebbert MTW, Josephs KA, Litvan I, Graff-Radford N, Ahlskog JE, Uitti RJ, van Gerpen JA, Boeve BF, Parks A, Ross OA, Dickson DW. Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype. Acta Neuropathologica. PMID 29926172 DOI: 10.1007/S00401-018-1878-Z |
0.702 |
|
| 2018 |
Kasanuki K, Josephs KA, Ferman TJ, Murray ME, Koga S, Konno T, Sakae N, Parks A, Uitti RJ, Van Gerpen JA, Graff-Radford NR, Wszolek ZK, Dickson DW. Diffuse Lewy body disease manifesting as corticobasal syndrome: A rare form of Lewy body disease. Neurology. PMID 29898972 DOI: 10.1212/Wnl.0000000000005828 |
0.576 |
|
| 2018 |
Ogaki K, Martens YA, Heckman MG, Koga S, Labbé C, Lorenzo-Betancor O, Wernick AI, Walton RL, Soto AI, Vargas ER, Nielsen HM, Fujioka S, Kanekiyo T, Uitti RJ, van Gerpen JA, et al. Multiple system atrophy and apolipoprotein E. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29442376 DOI: 10.1002/Mds.27297 |
0.347 |
|
| 2018 |
Kasanuki K, Ross OA, DeTure MA, Walton RL, Sanchez-Contreras M, Koga S, Murray ME, Rademakers R, Dickson DW. Relationships between lewy and tau pathologies in 375 consecutive non-Alzheimer's olfactory bulbs. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29322556 DOI: 10.1002/Mds.27250 |
0.559 |
|
| 2017 |
Shinohara M, Koga S, Konno T, Nix J, Shinohara M, Aoki N, Das P, Parisi JE, Petersen RC, Rosenberry TL, Dickson DW, Bu G. Distinct spatiotemporal accumulation of N-truncated and full-length amyloid-β42 in Alzheimer's disease. Brain : a Journal of Neurology. PMID 29161341 DOI: 10.1093/Brain/Awx284 |
0.373 |
|
| 2017 |
Koga S, Parks A, Kasanuki K, Sanchez-Contreras M, Baker MC, Josephs KA, Ahlskog JE, Uitti RJ, Graff-Radford N, van Gerpen JA, Wszolek ZK, Rademakers R, Dickson DW. Cognitive impairment in progressive supranuclear palsy is associated with tau burden. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29082658 DOI: 10.1002/Mds.27198 |
0.343 |
|
| 2017 |
Kasanuki K, Heckman MG, Diehl NN, Murray ME, Koga S, Soto A, Ross OA, Dickson DW. Regional analysis and genetic association of nigrostriatal degeneration in Lewy body disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28949048 DOI: 10.1002/Mds.27184 |
0.576 |
|
| 2017 |
Heckman MG, Kasanuki K, Diehl NN, Koga S, Soto A, Murray ME, Dickson DW, Ross OA. Parkinson's disease susceptibility variants and severity of Lewy body pathology. Parkinsonism & Related Disorders. PMID 28917824 DOI: 10.1016/J.Parkreldis.2017.09.009 |
0.612 |
|
| 2017 |
Koga S, Dickson DW. Recent advances in neuropathology, biomarkers and therapeutic approach of multiple system atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28860330 DOI: 10.1136/Jnnp-2017-315813 |
0.45 |
|
| 2017 |
Mishima T, Koga S, Lin WL, Kasanuki K, Castanedes-Casey M, Wszolek ZK, Oh SJ, Tsuboi Y, Dickson DW. Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy. Journal of Neuropathology and Experimental Neurology. 76: 676-682. PMID 28789478 DOI: 10.1093/Jnen/Nlx049 |
0.404 |
|
| 2017 |
Koga S, Parks A, Dickson DW. Reply re: "Profile of cognitive impairment and underlying pathology in multiple system atrophy". Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28671292 DOI: 10.1002/Mds.27084 |
0.314 |
|
| 2017 |
Mishima T, Kasanuki K, Koga S, Castanedes-Casey M, Wszolek ZK, Tsuboi Y, Dickson DW. Reduced orexin immunoreactivity in Perry syndrome and multiple system atrophy. Parkinsonism & Related Disorders. PMID 28651750 DOI: 10.1016/J.Parkreldis.2017.06.003 |
0.407 |
|
| 2017 |
Koga S, Ono M, Sahara N, Higuchi M, Dickson DW. Fluorescence and autoradiographic evaluation of tau PET ligand PBB3 to α-synuclein pathology. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28440890 DOI: 10.1002/Mds.27013 |
0.396 |
|
| 2017 |
Ono M, Sahara N, Kumata K, Ji B, Ni R, Koga S, Dickson DW, Trojanowski JQ, Lee VM, Yoshida M, Hozumi I, Yoshiyama Y, van Swieten JC, Nordberg A, Suhara T, et al. Distinct binding of PET ligands PBB3 and AV-1451 to tau fibril strains in neurodegenerative tauopathies. Brain : a Journal of Neurology. PMID 28087578 DOI: 10.1093/Brain/Aww339 |
0.44 |
|
| 2016 |
Koga S, Sanchez-Contreras M, Josephs KA, Uitti RJ, Graff-Radford N, van Gerpen JA, Cheshire WP, Wszolek ZK, Rademakers R, Dickson DW. Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28009087 DOI: 10.1002/Mds.26809 |
0.367 |
|
| 2016 |
Koga S, Parks A, Uitti RJ, van Gerpen JA, Cheshire WP, Wszolek ZK, Dickson DW. Profile of cognitive impairment and underlying pathology in multiple system atrophy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27859650 DOI: 10.1002/Mds.26874 |
0.363 |
|
| 2016 |
Koga S, Dickson DW, Bieniek KF. Chronic Traumatic Encephalopathy Pathology in Multiple System Atrophy. Journal of Neuropathology and Experimental Neurology. PMID 27543120 DOI: 10.1093/Jnen/Nlw073 |
0.7 |
|
| 2016 |
Labbé C, Heckman MG, Lorenzo-Betancor O, Murray ME, Ogaki K, Soto-Ortolaza AI, Walton RL, Fujioka S, Koga S, Uitti RJ, van Gerpen JA, Petersen RC, Graff-Radford NR, Younkin SG, Boeve BF, et al. MAPT haplotype diversity in multiple system atrophy. Parkinsonism & Related Disorders. PMID 27374978 DOI: 10.1016/J.Parkreldis.2016.06.010 |
0.624 |
|
| 2016 |
Koga S, Josephs KA, Ogaki K, Labbé C, Uitti RJ, Graff-Radford N, van Gerpen JA, Cheshire WP, Aoki N, Rademakers R, Wszolek ZK, Ross OA, Dickson DW. Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-C. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26841329 DOI: 10.1002/Mds.26499 |
0.408 |
|
| 2015 |
Ogaki K, Koga S, Heckman MG, Fiesel FC, Ando M, Labbé C, Lorenzo-Betancor O, Moussaud-Lamodière EL, Soto-Ortolaza AI, Walton RL, Strongosky AJ, Uitti RJ, McCarthy A, Lynch T, Siuda J, et al. Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology. PMID 26561290 DOI: 10.1212/Wnl.0000000000002170 |
0.402 |
|
| 2015 |
Ogaki K, Koga S, Aoki N, Lin W, Suzuki K, Ross OA, Dickson DW. Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26227820 DOI: 10.1111/Neup.12230 |
0.418 |
|
| 2015 |
Koga S, Aoki N, Uitti RJ, van Gerpen JA, Cheshire WP, Josephs KA, Wszolek ZK, Langston JW, Dickson DW. When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients. Neurology. 85: 404-12. PMID 26138942 DOI: 10.1212/Wnl.0000000000001807 |
0.437 |
|
| 2015 |
Aoki N, Boyer PJ, Lund C, Lin WL, Koga S, Ross OA, Weiner M, Lipton A, Powers JM, White CL, Dickson DW. Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein. Acta Neuropathologica. 130: 93-105. PMID 25962793 DOI: 10.1007/S00401-015-1442-Z |
0.48 |
|
| 2014 |
Koga S, Kojima A, Ishikawa C, Kuwabara S, Arai K, Yoshiyama Y. Effects of diet-induced obesity and voluntary exercise in a tauopathy mouse model: implications of persistent hyperleptinemia and enhanced astrocytic leptin receptor expression. Neurobiology of Disease. 71: 180-92. PMID 25132556 DOI: 10.1016/j.nbd.2014.08.015 |
0.405 |
|
| 2014 |
Koga S, Kojima A, Kuwabara S, Yoshiyama Y. Immunohistochemical analysis of tau phosphorylation and astroglial activation with enhanced leptin receptor expression in diet-induced obesity mouse hippocampus. Neuroscience Letters. 571: 11-6. PMID 24785100 DOI: 10.1016/j.neulet.2014.04.028 |
0.455 |
|
| 2013 |
Sekiguchi Y, Misawa S, Shibuya K, Mitsuma S, Hirano S, Ohmori S, Koga S, Iwai Y, Beppu M, Kuwabara S. Patterns of sensory nerve conduction abnormalities in Fisher syndrome: more predominant involvement of group Ia afferents than skin afferents. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 124: 1465-9. PMID 23474054 DOI: 10.1016/j.clinph.2013.01.020 |
0.351 |
|
| 2012 |
Koga S, Sekiguchi Y, Kanai K, Mutoh M, Kuwabara S. [Case of adult onset vanishing white matter disease developed after minor head trauma]. Rinshō Shinkeigaku = Clinical Neurology. 52: 561-6. PMID 22975854 DOI: DN/JST.JSTAGE/clinicalneurol/52.561 |
0.405 |
|
| 2012 |
Kanai K, Shibuya K, Sato Y, Misawa S, Nasu S, Sekiguchi Y, Mitsuma S, Isose S, Fujimaki Y, Ohmori S, Koga S, Kuwabara S. Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. 83: 734-8. PMID 22566594 DOI: 10.1136/jnnp-2011-301782 |
0.331 |
|
| 2012 |
Nasu S, Misawa S, Sekiguchi Y, Shibuya K, Kanai K, Fujimaki Y, Ohmori S, Mitsuma S, Koga S, Kuwabara S. Different neurological and physiological profiles in POEMS syndrome and chronic inflammatory demyelinating polyneuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 83: 476-9. PMID 22338030 DOI: 10.1136/jnnp-2011-301706 |
0.371 |
|
| 2012 |
Koga S, Kojima S, Kishimoto T, Kuwabara S, Yamaguchi A. Over-expression of map kinase phosphatase-1 (MKP-1) suppresses neuronal death through regulating JNK signaling in hypoxia/re-oxygenation. Brain Research. 1436: 137-46. PMID 22197701 DOI: 10.1016/j.brainres.2011.12.004 |
0.316 |
|
| 2011 |
Koga S, Ikeda K, Nakagomi D, Mori M, Kuwabara S, Nakajima H. A patient with neuromyelitis optica with positive anti-Ro (SS-A) antibody presenting with intractable hiccup and nausea. Modern Rheumatology. 21: 561-2. PMID 21399980 DOI: 10.1007/s10165-011-0438-3 |
0.341 |
|
| 2010 |
Sawai S, Misawa S, Kobayashi M, Kanai K, Isose S, Shibuya K, Sekiguchi Y, Nasu S, Noto Y, Fujimaki Y, Koga S, Ohtani R, Kuwabara S. Multifocal conduction blocks in sarcoid peripheral neuropathy. Internal Medicine (Tokyo, Japan). 49: 471-4. PMID 20190486 DOI: JST.JSTAGE/internalmedicine/49.2894 |
0.394 |
|
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