受賞

論文発表

• Shibata M, Hoshino R, Shimizu C, Sato M, Furuta N, Ikeda Y. Lacosamide-induced sinus node dysfunction followed by severe agranulocytosis. BMC Neurol. 2021; 21(1): 217.
• Shibata M, Makioka K, Hamaguchi Y, Ikeda Y. Favourable complete remission of anti-OJ antibody-positive myositis after lung cancer resection. Rheumatology (Oxford). 2022; 61: e77-e79.
• Hirayanagi K, Ozaki H, Tsukagoshi S, Furuta N, Ikeda Y. Porphyrins ameliorate spinocerebellar ataxia type 36 GGCCTG repeat expansion-mediated cytotoxicity. Neurosci Res. 2021; 171: 92-102.
• Aoki S, Nagashima K, Shibata M, Kasahara H, Fujita Y, Hashiguchi A, Takashima H, Ikeda Y. Sibling Cases of Charcot-Marie-Tooth Disease Type 4H with a Homozygous FGD4 Mutation and Cauda Equina Thickening. Intern Med. 2021; 60(24): 3975-3981.
• Urushida Y, Ishikawa D, Yanaizumi M, Nakamura T, Amari M, Kawarabayashi T, Tosaka M, Ikeda Y, Takatama M, Shoji M. IgG4-related hypothalamo-hypophysitis. eNeurologicalSci. 2021; 24: 100362.
• Urushida Y, Kikuchi Y, Shimizu C, Amari M, Kawarabayashi T, Nakamura T, Ikeda Y, Takatama M, Shoji M. Improved Neuroimaging Findings and Cognitive Function in a Case of High-altitude Cerebral Edema. Intern Med. 2021; 60(8): 1299-1302.
• Hoshino R, Furuta M, Shibata M, Wakamatsu I, Nagashima K, Yamaguchi R, Ikeda Y. Vanishing tumefactive ANCA-associated hypertrophic pachymeningitis: A case report. Clin Neurol Neurosurg. 2022; 212: 107070.
• Ikeda M, Okamoto K, Suzuki K, Amari M, Takai E, Takatama M, Yokoo H, Ishibashi S, Ikeda Y. Polygenic variants related to familial hypobetalipoproteinemia in a patient with Alzheimer’s disease homozygotic for the APOE ε2 allele presenting multiple cortical superficial siderosis and recurrent lobar hemorrhages. Neurogenetics. 2022; 23(1): 69-71.
• Ikeda M, Okamoto K, Suzuki K, Takai E, Kasahara H, Furuta N, Furuta M, Tashiro Y, Shimizu C, Takatama S, Naito I, Sato M, Sakai Y, Takahashi M, Amari M, Takatama M, Higuchi T, Tsushima Y, Yokoo H, Kurabayashi M, Ishibashi S, Ishii K, Ikeda Y. Recurrent Lobar Hemorrhages and Multiple Cortical Superficial Siderosis in a Patient of Alzheimer’s Disease With Homozygous APOE ε2 Allele Presenting Hypobetalipoproteinemia and Pathological Findings of 18F-THK5351 Positron Emission Tomography: A Case Report. Front Neurol. 2021; 12: 645625.
• Ikeda M, Kodaira S, Kasahara H, Takai E, Nagashima K, Fujita Y, Makioka K, Hirayanagi K, Furuta N, Furuta M, Sanada E, Kobayashi A, Harigaya Y, Nagamine S, Hattori N, Tashiro Y, Kishi K, Shimada H, Suto T, Tanaka H, Sakai Y, Yamazaki T, Tanaka Y, Aihara Y, Amari M, Yamaguchi H, Okamoto K, Takatama M, Ishii K, Higuchi T, Tsushima Y, Ikeda Y. Cerebral Microbleeds, Cerebrospinal Fluid, and Neuroimaging Markers in Clinical Subtypes of Alzheimer’s Disease. Front Neurol. 2021; 12: 543866.
• Nakahata N, Nakamura T, Kawarabayashi T, Seino Y, Ichii S, Ikeda Y, Amari M, Takatama M, Murashita K, Ihara K, Itoh K, Nakaji S, Shoji M. Age-Related Cognitive Decline and Prevalence of Mild Cognitive Impairment in the Iwaki Health Promotion Project. J Alzheimers Dis. 2021; 84(3): 1233-1245.
• Perez BA, Shorrock HK, Banez-Coronel M, Zu T, Romano LE, Laboissonniere LA, Reid T, Ikeda Y, Reddy K, Gomez CM, Bird T, Ashizawa T, Schut LJ, Brusco A, Berglund JA, Hasholt LF, Nielsen JE, Subramony SH, Ranum LP. CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity. EMBO Mol Med. 2021; 13(11): e14095.
• Hoshino K, Sweadner KJ, Kawarai T, Saute JA, Freitas J, Damásio J, Donis KC, Kimura K, Fukuda H, Hayashi M, Higuchi T, Ikeda Y, Ozelius LJ, Kaji R. Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations. Neurol Genet. 2021; 7(2): e562.
• Hoffmann T, Rahfeld JU, Schenk M, Ponath F, Makioka K, Hutter-Paier B, Lues I, Lemere CA, Schilling S. Combination of the Glutaminyl Cyclase Inhibitor PQ912 (Varoglutamstat) and the Murine Monoclonal Antibody PBD-C06 (m6) Shows Additive Effects on Brain Aβ Pathology in Transgenic Mice. Int J Mol Sci. 2021; 22:11791.
• Maehara T, Mizuno T, Tokoro M, Hara T, Tomita Y, Makioka K, Motegi SI, Yamazaki A, Matsumura N, Nobusawa S, Yokoo H. An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis. Neuropathology. 2022
• Kuriyama Y, Shimizu A, Oka H, Sato M, Makioka K, Ikota H, Yanagisawa K, Tokue Y, Tsukagoshi H, Motegi SI. Erythema nodosum-like eruption in coronavirus disease 2019: A case report and literature review of Asian countries. J Dermatol. 2021; 48:1588-1592.

総説

• 池田佳生.　特集：高齢者に特徴的な認知症　PSPとCBDの診断.　老年内科　2021; 3(6): 716-724.

著書

• 池田佳生.　常染色体劣性遺伝性、X染色体連鎖性の失調症.　 脳神経内科診断ハンドブック　中外医学社　2022, pp 166-169.
• 池田佳生.　18-6-3 脊髄小脳変性症　1) 多系統萎縮症.　内科学　第12版　朝倉書店　2022, pp Ⅴ-283-287.
• 池田佳生.　18-6-3脊髄小脳変性症　2) 皮質性小脳萎縮症.　内科学　第12版　朝倉書店　2022, pp Ⅴ-287-288.
• 池田佳生.　18-6-3脊髄小脳変性症　3) 遺伝性脊髄小脳変性症.　内科学　第12版　朝倉書店　2022, pp Ⅴ-288-292.

市民講演会や患者会での講演

• 藤田行雄. パーキンソン病　〜正しく知って上手に付き合う〜.　パーキンソン病　友の会　医療講演会　2021.8.25 （Web）
• 佐藤正行. 脊髄小脳変性症についてとリハビリテーション. 難病（多系統萎縮症・脊髄小脳変性症）療養相談会・交流会　2021.11.26（前橋）