Publications

  1. Kawazoe M, Koga S, Sekiya H, Josephs KA, Graff-Radford NR, Dickson DW. Disproportionately Enlarged Subarachnoid-Space Hydrocephalus on MRI in Pathologically Confirmed Progressive Supranuclear Palsy. Neurol Clin Pract. 2025 Apr; 15 (2):e200431 Epub 2025 Feb 20
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  2. 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, Bu G, Dickson DW, Ross OA, Springer W. Genome-wide association analysis identifies APOE as a mitophagy modifier in Lewy body disease. Alzheimers Dement. 2025 Apr; 21 (4):e70198
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  3. Valentino RR, Koga S, Soto-Beasley AI, Ono D, Wieczorek MA, Johnson PW, White LJ, Watkins MM, Murray ME, Kasanuki K, McLean PJ, Springer W, Uitti RJ, Fields JA, Botha H, Ramanan VK, Kantarci K, Lowe VJ, Jack CR Jr, Bras J, Guerreiro R, Ertekin-Taner N, Savica R, Graff-Radford J, Petersen RC, Parisi JE, Reichard RR, Graff-Radford NR, Ferman TJ, Boeve BF, Wszolek ZK, Dickson DW, Heckman MG, Ross OA. Genome-wide association study of neuropathological features in Lewy body disease. Brain. 2025 Mar 17 [Epub ahead of print]
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  4. Liskey D, Maier AR, Koga S, Irani S, Graff-Radford N, Josephs KA, Dickson DW, Roemer SF. Cortical variant multiple sclerosis presenting clinically as Lewy body dementia. J Neuropathol Exp Neurol. 2025 Mar 6 Epub 2025 Mar 06
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  5. Ono D, Sekiya H, Maier AR, Murray ME, Koga S, Dickson DW. Parkinsonism in Alzheimer's disease without Lewy bodies in association with nigral neuron loss: A data-driven clinicopathologic study. Alzheimers Dement. 2025 Mar; 21 (3):e14628
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  6. Cheshire WP, Tipton PW, Koga S, Sekiya H, Uitti RJ, Ross OA, Heckman MG, Sledge HJ, Dickson DW. Occupational histories in neuropathologically confirmed multiple system atrophy. Clin Auton Res. 2025 Jan 23 [Epub ahead of print]
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  7. Murakami A, Koga S, Fujioka S, White AE, Bieniek KF, Sekiya H, DeJesus-Hernandez M, Finch NA, van Blitterswijk M, Nakamura M, Tsuboi Y, Murray ME, Wszolek ZK, Dickson DW. Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study. Brain Pathol. 2025 Jan; 35 (1):e13286 Epub 2024 July 10
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  8. Pettersson SD, Koga S, Ali S, Enriquez-Marulanda A, Taussky P, Ogilvy CS. Cerebral Artery Overexpression of the NMUR1 Gene Is Associated with Moyamoya Disease: A Weighted Gene Co-Expression Network Analysis. Cerebrovasc Dis. 2025; 54 (1):1-10 Epub 2024 Feb 24
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  9. Bayram E, Coughlin DG, Koga S, Ross OA, Litvan I, Dickson DW. Sex differences for regional pathology in people with a high likelihood of Lewy body dementia phenotype based on underlying pathology. Alzheimers Dement (Amst). 2025 Jan-Mar; 17 (1):e70083 Epub 2025 Jan 29
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  10. Sekiya H, Tipton PW, Kawazoe M, Koga S, Murakami A, Maier AR, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW. Current Landscape of Clinical Diagnosis in Multiple System Atrophy: A 15-Year Analysis From 2008 to 2022. Neurology. 2024 Dec 10; 103 (11):e210021 Epub 2024 Nov 12
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  11. Jin Y, Wixom AQ, Li Z, Liu Y, Koga S, Sekiya H, Santhakumar H, Bu G, Dickson DW, Zhao N. Basic Science and Pathogenesis. Alzheimers Dement. 2024 Dec; 20 Suppl 1:e092756
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  12. Jin Y, Li F, Li Z, Ikezu TC, O'Leary J, Selvaraj M, Zhu Y, Martens YA, Koga S, Santhakumar H, Li Y, Lu W, You Y, Lolo K, DeTure M, Beasley AI, Davis MD, McLean PJ, Ross OA, Kanekiyo T, Ikezu T, Caulfield T, Carr J, Wszolek ZK, Bu G, Dickson DW, Zhao N. Modeling Lewy body disease with SNCA triplication iPSC-derived cortical organoids and identifying therapeutic drugs. Sci Adv. 2024 Sep 13; 10 (37):eadk3700 Epub 2024 Sept 11
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  13. Tamvaka N, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Uitti RJ, Parfitt F, Graff-Radford MR, Wszolek ZK, Graff-Radford N, Valentino RR, Ross OA. Associations of mitochondrial genomic variation with successful neurological aging. Mitochondrion. 2024 Sep; 78:101948. Epub 2024 Aug 22.
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  14. Ono D, Dickson DW, Koga S. Evaluating the efficacy of few-shot learning for GPT-4Vision in neurodegenerative disease histopathology: A comparative analysis with convolutional neural network model. Neuropathol Appl Neurobiol. 2024 Aug; 50 (4):e12997
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  15. Is Ö, Wang X, Reddy JS, Min Y, Yilmaz E, Bhattarai P, Patel T, Bergman J, Quicksall Z, Heckman MG, Tutor-New FQ, Can Demirdogen B, White L, Koga S, Krause V, Inoue Y, Kanekiyo T, Cosacak MI, Nelson N, Lee AJ, Vardarajan B, Mayeux R, Kouri N, Deniz K, Carnwath T, Oatman SR, Lewis-Tuffin LJ, Nguyen T, Alzheimer’s Disease Neuroimaging Initiative, Carrasquillo MM, Graff-Radford J, Petersen RC, Jr Jack CR, Kantarci K, Murray ME, Nho K, Saykin AJ, Dickson DW, Kizil C, Allen M, Ertekin-Taner N. Gliovascular transcriptional perturbations in Alzheimer's disease reveal molecular mechanisms of blood brain barrier dysfunction. Nat Commun. 2024 Jun 20; 15(1):4758.
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  16. 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, Christopher EA, DeTure M, Seeley WW, Lee EB, Frosch MP, Molina-Porcel L, Gefen T, Redding-Ochoa J, Ghetti B, Robinson AC, Kobylecki C, Rowe JB, Beach TG, Teich AF, Keith JL, Bodi I, Halliday GM, Gearing M, Arzberger T, Morris CM, White CL 3rd, Mechawar N, Boluda S, MacKenzie IR, McLean C, Cykowski MD, Wang SJ, Graff C, Nagra RM, Kovacs GG, Giaccone G, Neumann M, Ang LC, Carvalho A, Morris HR, Rademakers R, Hardy JA, Dickson DW, Rohrer JD, Ross OA, Pick's disease International Consortium. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study. Lancet Neurol. 2024 May; 23 (5):487-499
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  17. 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. 2024 Apr; 44 (2):115-125 Epub 2023 July 31
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  18. 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, Lowe VJ, Jack CR, Ertekin-Taner N, Savica R, Graff-Radford J, Petersen RC, Parisi JE, Reichard RR, Graff-Radford NR, Ferman TJ, Boeve BF, Wszolek ZK, Dickson DW, Ross OA, Heckman MG. Role of GBA variants in Lewy body disease neuropathology. Acta Neuropathol. 2024 Mar 12; 147 (1):54
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  19. Sekiya H, Koga S, Murakami A, DeTure M, Ross OA, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW. Frequency of Comorbid Pathologies and Their Clinical Impact in Multiple System Atrophy. Mov Disord. 2024 Feb; 39 (2):380-390 Epub 2023 Nov 20
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  20. 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, Josephs KA. Clinicopathologic features of a novel star-shaped transactive response DNA-binding protein 43 (TDP-43) pathology in the oldest old. J Neuropathol Exp Neurol. 2023 Dec 22; 83 (1):36-52
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  21. Sekiya H, Koga S, Murakami A, Kawazoe M, Kim M, Martin NB, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW. Validation Study of the MDS Criteria for the Diagnosis of Multiple System Atrophy in the Mayo Clinic Brain Bank. Neurology. 2023 Dec 12; 101 (24):e2460-e2471 Epub 2023 Oct 10
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  22. Kawazoe M, Koga S, Dickson DW. Progressive supranuclear palsy can mimic idiopathic normal pressure hydrocephalus: A case series. J Neuropathol Exp Neurol. 2023 Nov 20; 82 (12):1033-1036
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  23. 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 WDJ, Ross OA, Pihlstrom L. Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease. Brain. 2023 Oct 3; 146 (10):4077-4087
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  24. Hou X, Chen TH, Koga S, Bredenberg JM, Faroqi AH, Delenclos M, Bu G, Wszolek ZK, Carr JA, Ross OA, McLean PJ, Murray ME, Dickson DW, Fiesel FC, Springer W. Alpha-synuclein-associated changes in PINK1-PRKN-mediated mitophagy are disease context dependent. Brain Pathol. 2023 Sep; 33 (5):e13175 Epub 2023 May 31
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  25. Cheshire WP, Koga S, Tipton PW, Sekiya H, Ross OA, Uitti RJ, Josephs KA, Dickson DW. Cancer in pathologically confirmed multiple system atrophy. Clin Auton Res. 2023 Aug; 33 (4):451-458 Epub 2023 May 13
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  26. Koga S, Murakami A, Martin NB, Dickson DW. The frequency and distribution of TDP-43 pathology in argyrophilic grain disease. J Neuropathol Exp Neurol 2023 Jul 20; 82 (8):739-741
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  27. Shir D, Pham NTT, 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, Josephs KA, Whitwell J, Graff-Radford J. Clinicoradiologic and Neuropathologic Evaluation of Corticobasal Syndrome. Neurology. 2023 Jul 18; 101 (3):e289-e299 Epub 2023 June 02
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  28. Koga S, Murakami A, Soto-Beasley AI, Walton RL, Baker MC, Castanedes-Casey M, Josephs KA, Ross OA, Dickson DW. Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies. Acta Neuropathol Commun. 2023 Jul 12; 11 (1):117 Epub 2023 July 12
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  29. 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 Neuropathol Commun. 2023 Jul 6; 11 (1):109 Epub 2023 July 06
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  30. Martin NB, Sekiya H, Kim M, Dickson DW, Koga S. Brain Bank Questionnaire Helps in Differential Diagnosis of Movement Disorders: An Autopsy Study of 150 Patients. Mov Disord Clin Pract. 2023 Jul; 10 (7):1131-1135 Epub 2023 May 29
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  31. Dulski J, Koga S, Liberski PP, Sitek EJ, Butala AA, Slawek J, Dickson DW, Wszolek ZK. Perry Disease: Expanding the Genetic Basis. Mov Disord Clin Pract. 2023 Jul; 10 (7):1136-1142 Epub 2023 June 22
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  32. Dulski J, Koga S, Prudencio M, Tipton PW, Ali S, Strongosky AJ, Rose JH, Parrales ZA, Dunmore JA, Jansen-West K, Petrucelli L, Dickson DW, Wszolek ZK. Perry syndrome: Novel DCTN1 mutation in a large kindred and first observation of prodromal disease. Parkinsonism Relat Disord. 2023 Jul; 112:105481 Epub 2023 June 13
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  33. Koga S, Metrick MA 2nd, Golbe LI, Santambrogio A, Kim M, Soto-Beasley AI, Walton RL, Baker MC, De Castro CF, DeTure M, Russell D, Navia BA, Sandiego C, Ross OA, Vendruscolo M, Caughey B, Dickson DW. Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration. Acta Neuropathol Commun. 2023 Jun 1; 11 (1):88 Epub 2023 June 01
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  34. Kim M, Sekiya H, Yao G, Martin NB, Castanedes-Casey M, Dickson DW, Hwang TH, Koga S. Diagnosis of Alzheimer Disease and Tauopathies on Whole-Slide Histopathology Images Using a Weakly Supervised Deep Learning Algorithm. Lab Invest. 2023 Jun; 103 (6):100127 Epub 2023 Mar 06
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  35. Meneses AD, Koga S, Li Z, O'Leary J, Li F, Chen K, Murakami A, Qiao W, Kurti A, Heckman MG, White L, Xie M, Chen Y, Finch NA, Lim MJ, Delenclos M, DeTure MA, Linares C, Martin NB, Ikezu TC, van Blitterswijk MM, Wu LJ, McLean PJ, Rademakers R, Ross OA, Dickson DW, Bu G, Zhao N. APOE2 Exacerbates TDP-43 Related Toxicity in the Absence of Alzheimer Pathology. Ann Neurol. 2023 Apr; 93 (4):830-843 Epub 2023 Jan 10
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  36. Martin NB, Koga S, Appleby BS, Sekiya H, Dickson D. Creutzfeldt-Jakob Disease Misdiagnosed as Multiple System Atrophy. Mov Disord Clin Pract. 2023 Mar; 10 (3):496-500 Epub 2023 Jan 20
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  37. Dulski J, Koga S, Dickson DW, Wszolek ZK. Report of A Family with Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) Without Mutations in CSF1R, AARS1 or AARS2. Mov Disord Clin Pract. 2023 Feb; 10 (2):307-312 Epub 2023 Jan 10
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  38. Buciuc M, Koga S, Pham NTT, Duffy JR, Knopman DS, Ali F, Boeve BF, Graff-Radford J, Botha H, Lowe VJ, Nguyen A, Reichard RR, Dickson DW, Petersen RC, Whitwell JL, Josephs KA. The many faces of globular glial tauopathy: A clinical and imaging study. Eur J Neurol. 2023 Feb; 30(2):321-333. Epub 2022 Nov 01.
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  39. Josephs KA, Koga S, Tosakulwong N, Weigand SD, Nha Pham TT, Baker M, Whitwell JL, Rademakers R, Petrucelli L, Dickson DW. Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer's disease. Free Neuropathol. 2023 Jan; 4:22 Epub 2023 Dec 08
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  40. Hoag T, Koga S, Dickson DW, Kumar R. Globular glial tauopathy presenting clinically as atypical parkinsonism with dementia: A clinicopathological case report. Clin Park Relat Disord. 2023; 9:100210 Epub 2023 July 12
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  41. Koga S, Ali S, Baker MC, Wierenga KJ, Dompenciel M, Dickson DW, Wszolek ZK. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia? Parkinsonism Relat Disord. 2022 Dec; 105:149-153 Epub 2022 Nov 11
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  42. Murakami A, Koga S, Sekiya H, Oskarsson B, Boylan K, Petrucelli L, Josephs KA, Dickson DW. Old age amyotrophic lateral sclerosis and limbic TDP-43 pathology. Brain Pathol. 2022 Nov; 32 (6):e13100 Epub 2022 June 17
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  43. Iacono D, Koga S, Peng H, Manavalan A, Daiker J, Castanedes-Casey M, Martin NB, Herdt AR, Gelb MH, Dickson DW, Lee CW. Galactosylceramidase deficiency and pathological abnormalities in cerebral white matter of Krabbe disease. Neurobiol Dis. 2022 Nov; 174:105862 Epub 2022 Sept 14
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  44. 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, Ellinghaus D, Evsyukov V, Flanagan ME, Franke A, Frosch MP, Gearing M, Gelpi E, van Gerpen JA, Ghetti B, Glass JD, Grinberg LT, Halliday G, Helbig I, Hollerhage M, Huitinga I, Irwin DJ, Keene DC, Kovacs GG, Lee EB, Levin J, Marti MJ, Mackenzie I, McKeith I, Mclean C, Mollenhauer B, Neumann M, Newell KL, Pantelyat A, Pendziwiat M, Peters A, Molina Porcel L, Rabano A, Matej R, Rajput A, Rajput A, Reimann R, Scott WK, Seeley W, Selvackadunco S, Simuni T, Stadelmann C, Svenningsson P, Thomas A, Trenkwalder C, Troakes C, Trojanowski JQ, Uitti RJ, White CL, Wszolek ZK, Xie T, Ximelis T, Yebenes J, Muller U, Schellenberg GD, Herms J, Kuhlenbaumer G, Hoglinger G, Alzheimer's Disease Genetics Consortium. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy. Mov Disord. 2022 Oct; 37 (10):2110-2121 Epub 2022 Aug 23
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  45. Sekiya H, Tsuji A, Hashimoto Y, Takata M, Koga S, Nishida K, Futamura N, Kawamoto M, Kohara N, Dickson DW, Kowa H, Toda T. Discrepancy between distribution of alpha-synuclein oligomers and Lewy-related pathology in Parkinson's disease. Acta Neuropathol Commun. 2022 Sep 6; 10 (1):133 Epub 2022 Sept 06
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  46. Reho P, Koga S, Shah Z, Chia R, Rademakers R, Dalgard CL, Boeve BF, Beach TG, Dickson DW, Ross OA, Scholz SW, International LBD Genomics Consortium//American Genome Center. GRN Mutations Are Associated with Lewy Body Dementia. Mov Disord. 2022 Sep; 37 (9):1943-1948 Epub 2022 July 10
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  47. Ali S, Tipton PW, Koga S, Middlebrooks EH, Josephs KA, Strongosky A, Dickson DW, Wszolek ZK. A novel CSF1R variant in a South Dakota family with CSF1R-related leukoencephalopathy. Parkinsonism Relat Disord 2022 Sep; 102:51-53 Epub 2022 July 31
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  48. Carlos AF, Sekiya H, Koga S, Pham NTT, Ali F, Botha H, Clark HM, Coon EA, Lowe V, Ahlskog JE, Trejo-Lopez JA, Dickson DW, Whitwell JL, Josephs KA. Tau-PET and multimodal imaging in clinically atypical multiple system atrophy masquerading as progressive supranuclear palsy. Parkinsonism Relat Disord. 2022 Aug; 101:9-14 Epub 2022 June 16
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  49. Sekiya H, Koga S, Otsuka Y, Chihara N, Ueda T, Sekiguchi K, Yoneda Y, Kageyama Y, Matsumoto R, Dickson DW. Clinical and pathological characteristics of later onset multiple system atrophy. J Neurol. 2022 Aug; 269 (8):4310-4321 Epub 2022 Mar 19
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  50. 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, Jack CR, Ertekin-Taner N, Savica R, Graff-Radford J, Petersen RC, Parisi JE, Reichard RR, Graff-Radford NR, Ferman TJ, Boeve BF, Wszolek ZK, Dickson DW, Ross OA. Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures. Acta Neuropathol Commun. 2022 Jul 14; 10 (1):103 Epub 2022 July 14
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  51. Koga S, Josephs KA, Aiba I, Yoshida M, Dickson DW. Neuropathology and emerging biomarkers in corticobasal syndrome. J Neurol Neurosurg Psychiatry. 2022 Jun 13; 93 (9):919-29 Epub 2022 June 13
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  52. Koga S, Ishaque M, Jeffrey Elias W, Shah BB, Murakami A, Dickson DW. Neuropathology of Parkinson's disease after focused ultrasound thalamotomy. NPJ Parkinsons Dis. 2022 May 12; 8 (1):59
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  53. Koga S, Aiba I. [Autonomic Dysfunction in Tauopathies]. Brain Nerve. 2022 Mar; 74 (3):257-262
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  54. Koga S, Murakami A, Josephs KA, Dickson DW. Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia. Neuropathology. 2022 Feb; 42 (1):82-89 Epub 2022 Jan 13
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  55. Koga S, Zhou X, Murakami A, Fernandez De Castro C, Baker MC, Rademakers R, Dickson DW. Concurrent tau pathologies in frontotemporal lobar degeneration with TDP-43 pathology. Neuropathol Appl Neurobiol. 2022 Feb; 48 (2):e12778 Epub 2021 Dec 10
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  56. Koga S, Ikeda A, Dickson DW. Deep learning-based model for diagnosing Alzheimer's disease and tauopathies. Neuropathol Appl Neurobiol. 2022 Feb; 48 (1):e12759 Epub 2021 Aug 31
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  57. Murakami A, Koga S, Dickson DW. Asymmetrical Primary Lateral Sclerosis Presenting as Corticobasal Syndrome. J Neuropathol Exp Neurol 2022 Jan 29; 81 (2):154-156
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  58. Meneses A, Koga S, O'Leary J, Dickson DW, Bu G, Zhao N. TDP-43 Pathology in Alzheimer's Disease. Mol Neurodegener. 2021 Dec 20; 16 (1):84
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  59. Koga S, Sekiya H, Kondru N, Ross OA, Dickson DW. Neuropathology and molecular diagnosis of Synucleinopathies. Mol Neurodegener. 2021 Dec 18; 16 (1):83
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  60. Koga S, Zhou X, Dickson DW. Machine learning-based decision tree classifier for the diagnosis of progressive supranuclear palsy and corticobasal degeneration. Neuropathol Appl Neurobiol. 2021 Dec; 47 (7):931-941 Epub 2021 Apr 07
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  61. Wu Y, Shao W, Todd TW, Tong J, Yue M, Koga S, Castanedes-Casey M, Librero AL, Lee CW, Mackenzie IR, Dickson DW, Zhang YJ, Petrucelli L, Prudencio M. Microglial lysosome dysfunction contributes to white matter pathology and TDP-43 proteinopathy in GRN-associated FTD. Cell Rep. 2021 Aug 24; 36 (8):109581
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  62. Koga S, Cheshire WP, Tipton PW, Driver-Dunckley ED, Wszolek ZK, Uitti RJ, Graff-Radford NR, van Gerpen JA, Dickson DW. Clinical features of autopsy-confirmed multiple system atrophy in the Mayo Clinic Florida brain bank. Parkinsonism Relat Disord. 2021 Aug; 89:155-161 Epub 2021 July 10
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  63. Rademakers R, Nicholson AM, Ren Y, Koga S, Nguyen HP, Brooks M, Qiao W, Quicksall ZS, Matchett B, Perkerson RB, Kurti A, Castanedes-Casey M, Phillips V, Librero AL, Fernandez De Castro CH, Baker MC, Roemer SF, Murray ME, Asmann Y, Fryer JD, Bu G, Dickson DW, Zhou X. Loss of Tmem106b leads to cerebellum Purkinje cell death and motor deficits. Brain Pathol 2021 May; 31 (3):e12945 Epub 2021 Mar 11
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  64. Wernick AI, Walton RL, Soto-Beasley AI, Koga S, Ren Y, Heckman MG, Milanowski LM, Valentino RR, Kondru N, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW, Ross OA. Investigating ELOVL7 coding variants in multiple system atrophy. Neurosci Lett. 2021 Apr 01; 749:135723. Epub 2021 Feb 15.
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  65. Valentino RR, Heckman MG, Johnson PW, Baker MC, Soto-Beasley AI, Walton RL, Koga S, Roemer SF, Suh E, Uitti RJ, Trojanowski JQ, Grossman M, Van Deerlin VM, Rademakers R, Wszolek ZK, Dickson DW, Ross OA. Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease. Neurology. 2021 Mar 30; 96 (13):e1755-e1760 Epub 2021 Feb 10
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  66. Koga S, Ghayal NB, Dickson DW. Deep Learning-Based Image Classification in Differentiating Tufted Astrocytes, Astrocytic Plaques, and Neuritic Plaques. J Neuropathol Exp Neurol. 2021 Mar 22; 80 (4):306-312
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  67. Wernick AI, Walton RL, Soto-Beasley AI, Koga S, Heckman MG, Valentino RR, Milanowski LM, Hoffman-Zacharska D, Koziorowski D, Hassan A, Uitti RJ, Cheshire WP, Singer W, Wszolek ZK, Dickson DW, Low PA, Ross OA. Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy. Clin Auton Res. 2021 Feb; 31 (1):117-125 Epub 2021 Jan 27
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  68. Jabbari E, Koga S, Valentino RR, Reynolds RH, Ferrari R, Tan MMX, Rowe JB, Dalgard CL, Scholz SW, Dickson DW, Warner TT, Revesz T, Hoglinger GU, Ross OA, Ryten M, Hardy J, Shoai M, Morris HR, PSP Genetics Group. Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study. Lancet Neurol. 2021 Feb; 20 (2):107-116 Epub 2020 Dec 17
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  69. Koga S, Dickson DW, Wszolek ZK. Capgras syndrome in dementia with Lewy bodies: a possible association of severe cortical Lewy body pathology. Neurol Neurochir Pol. 2021; 55 (6):592-594 Epub 2021 Nov 30
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  70. 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 Neuropathol Commun. 2020 Dec 7; 8 (1):218 Epub 2020 Dec 07
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  71. Valentino RR, Heckman MG, Johnson PW, Soto-Beasley AI, Walton RL, Koga S, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA. Association of mitochondrial genomic background with risk of Multiple System Atrophy. Parkinsonism Relat Disord. 2020 Dec; 81:200-204 Epub 2020 Oct 29
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  72. Prudencio M, Humphrey J, Pickles S, Brown AL, Hill SE, Kachergus JM, Shi J, Heckman MG, Spiegel MR, Cook C, Song Y, Yue M, Daughrity LM, Carlomagno Y, Jansen-West K, de Castro CF, DeTure M, Koga S, Wang YC, Sivakumar P, Bodo C, Candalija A, Talbot K, Selvaraj BT, Burr K, Chandran S, Newcombe J, Lashley T, Hubbard I, Catalano D, Kim D, Propp N, Fennessey S, Fagegaltier D, Phatnani H, Secrier M, Fisher EM, Oskarsson B, van Blitterswijk M, Rademakers R, Graff-Radford NR, Boeve BF, Knopman DS, Petersen RC, Josephs KA, Thompson EA, Raj T, Ward M, Dickson DW, Gendron TF, Fratta P, Petrucelli L, NYGC ALS Consortium. Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. J Clin Invest. 2020 Nov 2; 130 (11):6080-6092
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  73. 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, Rademakers R. Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin-deficient mice. EMBO Rep. 2020 Oct 5; 21 (10):e50197 Epub 2020 Aug 05
    View PubMed
  74. 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 Neuropathol Commun. 2020 Sep 17; 8 (1):162 Epub 2020 Sept 17
    View PubMed
  75. Koga S. [Neuropathology of Cerebellar Cortical Atrophy]. Brain Nerve. 2020 Sep; 72 (9):939-946
    View PubMed
  76. 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 Relat Disord. 2020 Aug; 77:64-69 Epub 2020 June 22
    View PubMed
  77. 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 Pathol. 2020 Jul; 30 (4):766-778 Epub 2020 Apr 14
    View PubMed
  78. Koga S, Roemer SF, Tipton PW, Low PA, Josephs KA, Dickson DW. Cerebrovascular pathology and misdiagnosis of multiple system atrophy: An autopsy study. Parkinsonism Relat Disord. 2020 Jun; 75:34-40 Epub 2020 May 16
    View PubMed
  79. 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. Mov Disord. 2020 May; 35 (5):890-894 Epub 2020 Mar 06
    View PubMed
  80. Saijo E, Metrick MA 2nd, 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, Ghetti B, Dickson DW, Caughey B. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathol. 2020 Jan; 139 (1):63-77 Epub 2019 Oct 16
    View PubMed
  81. Saijo E, Metrick MA 2nd, 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, Ghetti B, Dickson DW, Caughey B. Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathol. 2020 Jan; 139 (1):79-81
    View PubMed
  82. Koga S, Roemer SF, Kasanuki K, Dickson DW. Cerebrovascular pathology presenting as corticobasal syndrome: An autopsy case series of "vascular CBS". Parkinsonism Relat Disord. 2019 Nov; 68:79-84 Epub 2019 Sept 02
    View PubMed
  83. 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, Tabuchi H, Bieniek KF, Kawamura K, Zhang MR, Dickson DW, Mimura M, Kato M, Suhara T, Higuchi M. PET-detectable tau pathology correlates with long-term neuropsychiatric outcomes in patients with traumatic brain injury. Brain. 2019 Oct 1; 142 (10):3265-3279
    View PubMed
  84. 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. Mov Disord. 2019 Sep; 34(9):1325-1332. Epub 2019 Jun 24.
    View PubMed
  85. 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. J Neuropathol Exp Neurol. 2019 Aug 1; 78 (8):756-762
    View PubMed
  86. 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 Neurol. 2019 Jun 01; 76(6):710-717.
    View PubMed
  87. 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, Suhara T, Higuchi M. In vivo binding of a tau imaging probe, [(11) C]PBB3, in patients with progressive supranuclear palsy. Mov Disord. 2019 May; 34 (5):744-754 Epub 2019 Mar 20
    View PubMed
  88. 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 Neuropathol. 2018 Dec; 136 (6):873-885 Epub 2018 Sept 15
    View PubMed
  89. Koga S, Lin WL, Walton RL, Ross OA, Dickson DW. TDP-43 pathology in multiple system atrophy: colocalization of TDP-43 and alpha-synuclein in glial cytoplasmic inclusions. Neuropathol Appl Neurobiol. 2018 Dec; 44 (7):707-721 Epub 2018 May 09
    View PubMed
  90. 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, Murray ME, Reddy JS, Funk C, Price ND, Golde TE, Younkin SG, Asmann YW, Crook JE, Dickson DW, Ertekin-Taner N. Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy. Acta Neuropathol. 2018 Nov; 136(5):709-727. Epub 2018 Aug 22.
    View PubMed
  91. 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, Caselli RJ, Sanchez-Contreras MY, Rademakers R, Murray ME, Koga S, Dickson DW, Ross OA, Bu G. APOE epsilon2 is associated with increased tau pathology in primary tauopathy. Nat Commun. 2018 Oct 22; 9 (1):4388
    View PubMed
  92. 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 Neuropathol. 2018 Sep; 136 (3):389-404 Epub 2018 June 20
    View PubMed
  93. 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, Low PA, Singer W, Bu G, Dickson DW, Ross OA. Association study between multiple system atrophy and TREM2 p.R47H. Neurol Genet. 2018 Aug; 4(4):e257.
    View PubMed
  94. 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. 2018 Jul 17; 91 (3):e268-e279 Epub 2018 June 13
    View PubMed
  95. 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, Cheshire WP, Wszolek ZK, Low PA, Singer W, Dickson DW, Bu G, Ross OA. Multiple system atrophy and apolipoprotein E. Mov Disord. 2018 Apr; 33(4):647-650. Epub 2018 Feb 14.
    View PubMed
  96. 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. Mov Disord 2018 Feb; 33 (2):333-334 Epub 2018 Jan 11
    View PubMed
  97. Koga S, Dickson DW. Recent advances in neuropathology, biomarkers and therapeutic approach of multiple system atrophy. J Neurol Neurosurg Psychiatry. 2018 Feb; 89 (2):175-184 Epub 2017 Aug 31
    View PubMed
  98. 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. Mov Disord. 2017 Dec; 32 (12):1772-1779 Epub 2017 Oct 30
    View PubMed
  99. 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-beta42 in Alzheimer's disease. Brain. 2017 Dec 1; 140 (12):3301-3316
    View PubMed
  100. 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 Relat Disord. 2017 Nov; 44:79-84 Epub 2017 Sept 11
    View PubMed
  101. 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. Mov Disord. 2017 Nov; 32 (11):1584-1593 Epub 2017 Sept 26
    View PubMed
  102. 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 Relat Disord. 2017 Sep; 42:85-89 Epub 2017 June 12
    View PubMed
  103. 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. J Neuropathol Exp Neurol. 2017 Aug 1; 76 (8):676-682
    View PubMed
  104. Koga S, Ono M, Sahara N, Higuchi M, Dickson DW. Fluorescence and autoradiographic evaluation of tau PET ligand PBB3 to alpha-synuclein pathology. Mov Disord. 2017 Jun; 32 (6):884-892 Epub 2017 Apr 25
    View PubMed
  105. 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. Mov Disord. 2017 Mar; 32 (3):405-413 Epub 2016 Nov 15
    View PubMed
  106. 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, Zhang MR, Higuchi M. Distinct binding of PET ligands PBB3 and AV-1451 to tau fibril strains in neurodegenerative tauopathies. Brain. 2017 Mar 1; 140 (3):764-780
    View PubMed
  107. 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. Mov Disord. 2017 Feb; 32 (2):246-255 Epub 2016 Dec 23
    View PubMed
  108. Koga S. [The Nomenclature and Classification of Sporadic Spinocerebellar Degeneration]. Brain Nerve. 2016 Dec; 68: (12)1453-1457.
    View PubMed
  109. Koga S, Dickson DW, Bieniek KF. Chronic Traumatic Encephalopathy Pathology in Multiple System Atrophy. J Neuropathol Exp Neurol. 2016 Oct; 75 (10):963-970 Epub 2016 Aug 18
    View PubMed
  110. 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, Cheshire WP Jr, Low PA, Sandroni P, Coon EA, Singer W, Wszolek ZK, Dickson DW, Ross OA. MAPT haplotype diversity in multiple system atrophy. Parkinsonism Relat Disord. 2016 Sep; 30:40-5. Epub 2016 Jun 16.
    View PubMed
  111. Koga S, Josephs KA, Ogaki K, Labbe 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. Mov Disord. 2016 May; 31 (5):653-62 Epub 2016 Feb 03
    View PubMed
  112. 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. 2016 Feb; 36 (1):64-76 Epub 2015 July 31
    View PubMed
  113. 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, Opala G, Rudzinska M, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Puschmann A, Nishioka K, Funayama M, Hattori N, Parisi JE, Petersen RC, Graff-Radford NR, Boeve BF, Springer W, Wszolek ZK, Dickson DW, Ross OA. Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology. 2015 Dec 08; 85(23):2016-25. Epub 2015 Nov 11.
    View PubMed
  114. 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. 2015 Aug 4; 85 (5):404-12 Epub 2015 July 02
    View PubMed
  115. Aoki N, Boyer PJ, Lund C, Lin WL, Koga S, Ross OA, Weiner M, Lipton A, Powers JM, White CL 3rd, Dickson DW. Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with alpha-synuclein. Acta Neuropathol. 2015 Jul; 130 (1):93-105 Epub 2015 May 12
    View PubMed
  116. 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. Neurobiol Dis. 2014 Nov; 71:180-92 Epub 2014 Aug 15
    View PubMed
  117. 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. Neurosci Lett. 2014 Jun 13; 571:11-6 Epub 2014 Apr 28
    View PubMed
  118. Koga S, Sadahiro T, Ito S, Asahina M, Oda S. Aphonia due to vocal cord impairment induced by carbon monoxide poisoning. Acute Med Surg. 2014 Apr; 1 (2):119-121 Epub 2014 Jan 28
    View PubMed
  119. 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. Clin Neurophysiol. 2013 Jul; 124 (7):1465-9 Epub 2013 Mar 07
    View PubMed
  120. Koga S, Hasegawa H, Yasuda N, Lee K, Ueda M, Funabashi N, Arimura T, Kimura A, Nagai T, Kobayashi Y. [A case of mid-ventricular obstructive hypertrophic cardiomyopathy with apical aneurysm diagnosed after ventricular fibrillation] Shinzo. 2012; 44(11):1399-1404.
  121. Koga S, Ishiwada N, Honda Y, Okunushi T, Hishiki H, Ouchi K, Kohno Y. A case of meningoencephalitis associated with macrolide-resistant Mycoplasma pneumoniae infection. Pediatr Int. 2012 Oct; 54 (5):724-6
    View PubMed
  122. 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. J Neurol Neurosurg Psychiatry. 2012 Jul; 83 (7):734-8 Epub 2012 May 07
    View PubMed
  123. 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. J Neurol Neurosurg Psychiatry. 2012 May; 83 (5):476-9 Epub 2012 Feb 15
    View PubMed
  124. Furuya M, Tanaka R, Koga S, Yatabe Y, Gotoda H, Takagi S, Hsu YH, Fujii T, Okada A, Kuroda N, Moritani S, Mizuno H, Nagashima Y, Nagahama K, Hiroshima K, Yoshino I, Nomura F, Aoki I, Nakatani Y. Pulmonary cysts of Birt-Hogg-Dube syndrome: a clinicopathologic and immunohistochemical study of 9 families. Am J Surg Pathol. 2012 Apr; 36 (4):589-600
    View PubMed
  125. 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 Res. 2012 Feb 3; 1436:137-46 Epub 2011 Dec 08
    View PubMed
  126. Koga S, Sekiguchi Y, Kanai K, Mutoh M, Kuwabara S. [Case of adult onset vanishing white matter disease developed after minor head trauma]. Rinsho Shinkeigaku. 2012; 52 (8):561-6
    View PubMed
  127. Sakairi Y, Yoshino I, Okamoto T, Hoshino H, Yoshida S, Tanaka R, Koga S, Takahashi Y, Nakatani Y. A report on two surgical cases of pneumothorax lung in Birt-Hogg-Dube syndrome and a hypothesis of the pathogenesis of the syndrome Journal of the Japan Society for Pneumothorax and Cystic Lung Diseases. 2011; 11(1):25-28.
  128. Koga S, Furuya M, Nakatani Y. [Birt-Hogg-Dube syndrome]. Nihon Rinsho. 2010 Feb; 68 (2):361-9
    View PubMed
  129. 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. Intern Med. 2010; 49 (5):471-4 Epub 2010 Mar 01
    View PubMed
  130. Koga S, Furuya M, Takahashi Y, Tanaka R, Yamaguchi A, Yasufuku K, Hiroshima K, Kurihara M, Yoshino I, Aoki I, Nakatani Y. Lung cysts in Birt-Hogg-Dube syndrome: histopathological characteristics and aberrant sequence repeats. Pathol Int. 2009 Oct; 59 (10):720-8
    View PubMed