2019
2018
2017
2016
2015
2014
2013
2012
2011
2010
2009

2019年

＜論文＞

  1. Yamashiro K, Kurita N, Tanaka R, Ueno Y, Miyamoto N, Hira K, Nakajima S, Urabe T and Hattori N: Adequate Adherence to Direct Oral Anticoagulant is Associated with Reduced Ischemic Stroke Severity in Patients with Atrial Fibrillation. J Stroke Cerebrovasc Dis, 28:1773-1780, 2019.
  2. Ueno Y, Tateishi Y, Doijiri R, Kuriki A, Shimizu T, Kikuno M, Shimada Y, Takekawa H, Yamaguchi E, Koga M, Kamiya Y, Ihara M, Tsujino A, Hirata K, Toyoda K, Hasegawa Y, Hattori N and Urabe T: Large aortic arch plaques correlate with CHADS2 and CHA2DS2-VASc scores in cryptogenic stroke. Atherosclerosis, 284:181-186, 2019.
  3. Ueno Y, Miyamoto N, Yamashiro K, Tanaka R and Hattori N: Omega-3 Polyunsaturated Fatty Acids and Stroke Burden. Int J Mol Sci, 20, 2019.
  4. Taieb G, Mulero P, Psimaras D, van Oosten BW, Seebach JD, Marignier R, Pico F, Rigau V, Ueno Y, Duflos C, Fominykh V, Guiraud V, Lebrun-Frenay C, Camdessanche JP, Kerschen P, Ahle G, Tellez N, Rovira A, Hoang-Xuan K, Pelletier J, Labauge P and in cooperation with the French Cg: CLIPPERS and its mimics: evaluation of new criteria for the diagnosis of CLIPPERS. J Neurol Neurosurg Psychiatry, 2019.
  5. Sugiyama M, Ueno Y, Kamo H, Edahiro Y, Miyamoto N, Yamashiro K, Tanaka R, Shimo Y, Komatsu N and Hattori N: Specific mechanisms of subarachnoid hemorrhage accompanied by ischemic stroke in essential thrombocythemia: two case reports and a literature review. J Neurol, 266:1869-1878, 2019.
  6. Magami S, Miyamoto N, Ueno Y, Hira K, Tanaka R, Yamashiro K, Oishi H, Arai H, Urabe T and Hattori N: The Effects of Astrocyte and Oligodendrocyte Lineage Cell Interaction on White Matter Injury under Chronic Cerebral Hypoperfusion. Neuroscience, 406:167-175, 2019.
  7. Kamo H, Ueno Y, Sugiyama M, Miyamoto N, Yamashiro K, Tanaka R, Yokoyama K and Hattori N: Pontine hemorrhage accompanied by neuromyelitis optica spectrum disorder. J Neuroimmunol, 330:19-22, 2019.
  8. Kamo H, Ueno Y, Sugiyama M, Miyamoto N, Yamashiro K, Tanaka R and Hattori N: Temporal Profile of CT and T2*-Weighted Gradient-Echo MRI in a Patient with Unilateral Thalamostriate Vein Thrombosis. J Stroke Cerebrovasc Dis, 28:389-391, 2019.
  9. Inaba T, Miyamoto N, Hira K, Ueno Y, Yamashiro K, Watanabe M, Shimada Y, Hattori N and Urabe T: Protective Role of Levetiracetam Against Cognitive Impairment And Brain White Matter Damage in Mouse prolonged Cerebral Hypoperfusion. Neuroscience, 2019.
  10. Ikeda A, Shimada H, Nishioka K, Takanashi M, Hayashida A, Li Y, Yoshino H, Funayama M, Ueno Y, Hatano T, Sahara N, Suhara T, Higuchi M and Hattori N: Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features. Mov Disord, 34:568-574, 2019.
  11. Aoki J, Iguchi Y, Urabe T, Yamagami H, Todo K, Fujimoto S, Idomari K, Kaneko N, Iwanaga T, Terasaki T, Tanaka R, Yamamoto N, Tsujino A, Nomura K, Abe K, Uno M, Okada Y, Matsuoka H, Yamagata S, Yamamoto Y, Yonehara T, Inoue T, Yagita Y, Kimura K and Investigators ADS: Acute Aspirin Plus Cilostazol Dual Therapy for Noncardioembolic Stroke Patients Within 48 Hours of Symptom Onset. J Am Heart Assoc, 8:e012652, 2019.
  12. Tsuchiya M, Koh K, Ishida A, Ichinose Y, Shindo K, and Takiyama Y: A Japanese family with a novel nonsense mutation in the spastin gene associated with both cerebellar ataxia and cognitive impairment. J Neurol Sci 397:114-116, 2019.
  13. Miyabayashi T, Ochiai T, Suzuki N, Aoki M, Inui T, Okubo Y, Sato R, Togashi N, Takashima H, Ishiura H, Tsuji S, Koh K, Takiyama Y, and Haginoya K: A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy. J Hum Genet 64: 171-176, 2019.
  14. Koh K, Tsuchiya M, Nagasaka T, Shindo K, Takiyama Y: Decreasing 123I-ioflupane SPECT accumulation and 123I-MIBG myocardial scintigraphy uptake in a patient with a novel homozygous mutation in the ZFYVE26 gene. Neurol Sci 40: 429-431, 2019.
  15. Koh K, Ichinose Y, Ishiura H, Nan H, Mitsui J, Takahashi J, Sato W, Itoh Y, Hoshino K, JASPAC, Tsuji S, and Takiyama Y: PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia. J Hum Genet 64: 55-59, 2019.
  16. Nan H, Takaki R, Shimozono K, Ichinose Y, Koh K, and Takiyama Y: Clinical and genetic study of the first Japanese FTDP-17 patient with a mutation of +3 in intron 10 in the MAPT gene. Intern Med 58: 2397-2400, 2019.
  17. Nan H, Takaki R, Hata T, Ichinose Y, Tsuchiya M, Koh K, and Takiyama Y: Novel GARS mutation presenting as autosomal dominant intermediate Charcot-Marie-Tooth disease. J Peripher Nerv Syst 24: 156-160, 2019.
  18. Ichinose Y, Ishiura H, Tanaka M, Yoshimura J, Doi K, Umeda T, Yamauchi H, Tsuchiya M, Koh K, Yamashiro N, Mitsui J, Goto J, Onishi H, Ohtsuka T, Shindo K, Morishita S, Tsuji S, Takiyama Y: Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. Parkinsonism Relat Disord 61: 57-63, 2019.
  19. Hata T, Nagasaka T, Koh K, Tsuchiya M, Ichinose Y, Nan H, Shindo K, Takiyama Y: Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case report. BMC Neurol 19: 125, 2019.
  20. Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, Takeuchi H, Kawamoto M, Kohara N, Ando T, Ieda T, Kita Y, Kokubun N, Tsuboi Y, Katoh K, Kino Y, Katsuno M, Iwasaki Y, Yoshida M, Tanaka F, Suzuki IK, Frith MC, Matsumoto N, Sobue G: Long-read sequencing identifies GGC repeat expansion in human-specific NOTCH2NLC associated with neuronal intranuclear inclusion disease. Nat Genet 51: 1215-1221, 2019.
  21. Nan H, Ichinose Y, Tanaka M, Koh K, Ishiura H, Mitsui J, Mizukami H, Morimoto M, Hamada S, Ohtsuka T, Tsuji S, and Takiyama Y: UBAP1 mutations cause juvenile onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes. J Hum Genet 64: 1055-1065, 2019.
  22. Nan H, Natori T, Ichinose Y, Koh K, Kobayashi F, Shindo K, Hashiyada M, Adachi N, Yamagata Z, and Takiyama Y: Conjugal cerebellar type of multiple system atrophy: person-to-person transmission? Parkinsonism Relat Disord 69: 68-70, 2019.
  23. Koh K, Tsuchiya M, Nagasaka T, Shindo K, and Takiyama Y. Decreasing 123I-ioflupane SPECT accumulation and 123I-MIBG myocardial scintigraphy uptake in a patient with a novel homozygous mutation in the ZFYVE26 gene. Neurol Sci 40: 429-431, 2019.
  24. Shindo K, Sato T, Murata H, Ichinose Y, Hata T, and Takiyama Y. Spinocerebellar ataxia type 31 associated with REM sleep behavior disorder: a case report. BMC Neurol 19: 9-0, 2019.
  25. Koh K, Tsuchiya M, Nagasaka T, Shindo K, and Takiyama Y. Decreasing 123I-ioflupane SPECT accumulation and 123I-MIBG myocardial scintigraphy uptake in a patient with a novel homozygous mutation in the ZFYVE26 gene. Neurol Sci 40: 429-431, 2019.
  26. Nan H, Shimozono K, Ichinose Y, Tsuchiya M, Koh K, Hiraide M, and Takiyama Y. Exome sequencing reveals a novel homozygous frameshift mutation in the CYP7B1 gene in a Japanese patient with SPG5. Intern Med 58: 719-722, 2019.
  27. Shindo K, Tsuchiya M, Hata T, Ichinose Y, Koh K, Sone J, Nagasaka T, Sobue G, and Takiyama Y. Non-convulsive status epilepticus associated with neuronal intranuclear inclusion disease: a case report and literature review. Epilepsy Behav Case Rep 11: 103-106, 2019.
  28. Hata T, Nagasaka T, Koh K, Tsuchiya M, Ichinose Y, Nan H, Shindo K, Takiyama Y. Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene: a case report. BMC Neurology19 : 125, 2019.
  29. 名取高広, 新藤和雅, 長坂高村, 佐竹紅音, 森嶋悠人, 諏訪裕美, 村田博朗, 栗田尚史, 佐藤統子, 土屋　舞, 一瀬佑太, 羽田貴礼, 髙　紀信,　瀧山嘉久: 当科におけるプリオン蛋白遺伝子E200K変異家系の臨床・遺伝学的検討. Neuroinfection 24: 82-88, 2019.
  30. 山城亘央, 小尾公美子, 武田　清, 川上純範, 瀧山嘉久: レベチラセタムは半球間のバランスを調節しリハビリアウトカム改善に寄与する可能性がある. 脳神経内科 91: 498-503, 2019.

＜総説＞

  1. 髙　紀信, 南　海天, 一瀬佑太, 石浦浩之, 辻 省次, 瀧山嘉久: 研究者の最新動向　遺伝性痙性対麻痺の新規治療ターゲット探求のための原因遺伝子探索. Precision Medicine 2: 1247-1253, 2019.

2018年

＜論文＞

  1. Ueno Y, Tanaka R, Yamashiro K, Miyamoto N, Hira K, Kurita N, Sakurai M, Urabe T, Shimada K, Miyazaki T, Daida H and Hattori N: Age Stratification and Impact of Eicosapentaenoic Acid and Docosahexaenoic Acid to Arachidonic Acid Ratios in Ischemic Stroke Patients. J Atheroscler Thromb, 25:593-605, 2018.
  2. Ogawa T, Ueno Y, Kamo H, Miyamoto N, Yamashiro K, Tanaka R, Shimo Y and Hattori N: Conjugate Eye Deviation Caused by Upper Medial Medullary Infarction: A Case Report. J Stroke Cerebrovasc Dis, 27:e221-e223, 2018.
  3. Nakano F, Ueno Y, Suda A, Takanashi M, Yamashita A, Abe Y, Kon T, Miyamoto N, Yamashiro K, Tanaka R, Naito T, Yao T, Tamura N and Hattori N: Fatal ischemic stroke caused by cerebral small arteritis in a patient with giant cell arteritis. J Neurol Sci, 391:22-24, 2018.
  4. Kamo H, Miyamoto N, Otani H, Kurita N, Nakajima S, Ueno Y, Yamashiro K, Tanaka R and Hattori N: The Importance of Combined Antithrombotic Treatment for Capsular Warning Syndrome. J Stroke Cerebrovasc Dis, 27:3095-3099, 2018.
  5. Hira K, Ueno Y, Tanaka R, Miyamoto N, Yamashiro K, Inaba T, Urabe T, Okano H and Hattori N: Astrocyte-Derived Exosomes Treated With a Semaphorin 3A Inhibitor Enhance Stroke Recovery via Prostaglandin D2 Synthase. Stroke, 49:2483-2494, 2018.
  6. Daida K, Miyamoto N, Takagi H, Ueno Y, Yamashiro K, Tanaka R and Hattori N: Bilateral Caudate Nucleus Infarctions Following Upper Gastrointestinal Bleeding. J Stroke Cerebrovasc Dis, 27:e219-e220, 2018.
  7. Ishiura H, Doi K, Mitsui J, Yoshiumra J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koide R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita R, Tsuji S: Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy. Nat Genet 50: 581-590, 2018.
  8. Nan H, Takaki R, Ichinose Y, Tsuchiya M, Koh K, Hanyu S, Shindo K, and Takiyama Y: Novel SLC20A2 mutation in primary brain calcification with disturbance of sustained phonation and orofacial apraxia. J Neurol Sci 390: 1-3, 2018.
  9. Koh K, Ishiura H, Beppu M, Shimazaki H, Ichinose Y, Mitsui J, Kuwabara S, JASPAC, Tsuji S, and Takiyama Y: Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment. J Hum Genet 63: 1009-1013, 2018.
  10. Nan H, Shimozono K, Ichinose Y, Tsuchiya M, Koh K, Hiraide M, and Takiyama Y: Exome sequencing reveals a novel homozygous frameshift mutation in the CYP7B1 gene in a Japanese patient with SPG5. Intern Med 58: 719-722, 2018.
  11. Koh K, Ishiura H, Tsuji S, and Takiyama Y. JASPAC: Japan Spastic Paraplegia Research Consortium. Brain Sci 8: 153, 2018.
  12. Nan H, Takaki R, Hata T, Ichinose Y, Tsuchiya M, Koh K, and Takiyama Y: Novel GARS mutation presenting as autosomal dominant intermediate Charcot – Marie-Tooth disease. J Peripher Nerv Syst 24: 156-160, 2018.
  13. Shindo K, Satake A, Kurita N, Sato T, Tsuchiya M, Ichinose Y, Hata T, Koh K, Nagasaka T, and Takiyama Y. Sympathetic neurograms showing characteristics of both muscle and skin sympathetic nerve activity in a case with pure autonomic failure. Clin Auton Res 28: 347-349, 2018.
  14. Mukai M, Kishin Koh, Ohnuki Y, Nagata E, Takiyama Y, Takizawa S. Novel SPG11 mutations in a patient with symptoms mimicking multiple sclerosis. Intern Med 57: 3183-3186, 2018.
  15. 山城亘央，長坂高村，大石直輝，土屋　舞，高木隆助，小林史和，新藤和雅，瀧山嘉久：Ramsay Hunt症候群から播種性帯状疱疹に進展し，髄膜脳炎・脳梗塞を併発した90歳男性の剖検例. Brain Nerve 70 : 253-258, 2018.
  16. 佐藤統子，土屋　舞，一瀬佑太，山城亘央，新藤和雅，瀧山嘉久：硬膜瘻孔が確認できた脳表ヘモジデリン沈着症の1例. 山梨医学 45 : 14-17, 2018.
  17. 栗田尚史，佐竹紅音，高　紀信，羽田貴礼，小林史和，長坂高村，新藤和雅，瀧山嘉久：急性発症の失行・失語で発症した非けいれん性てんかん重積状態の一例. 山梨医学 45 : 11-13, 2018.
  18. 土屋　舞，新藤和雅，山城亘央，小林史和，長坂高村，瀧山嘉久：亜急性に進行する痙性対麻痺を呈し脊髄炎様画像所見を認めた局所性破傷風の1例. 臨床神経58：688-691, 2018.
  19. 下園啓介，一瀬佑太，南　海天，諏訪裕美，佐竹紅音，佐藤統子，羽田貴礼，土屋　舞，高　紀信，長坂高村，瀧山嘉久：新規REEP1遺伝子変異を認めたSPG31の1例. 山梨医科大学雑誌 33 : 63-68, 2018.

＜総説＞

  1. 高　紀信, 瀧山嘉久: Boucher – Neuhaeuser 症候群の新規原因遺伝子PNPLA6. 神経内科 88: 204-210, 2018.
  2. 高　紀信, 瀧山嘉久: 遺伝性痙性対麻痺の全国多施設共同研究体制: JASPAC. 難病と在宅ケア 24: 10-12, 2018.
  3. 一瀬佑太, 瀧山嘉久：遺伝性痙性対麻痺のITB (バクロフェン髄注) 療法. 難病と在宅ケア 24: 13-17, 2018.
  4. 瀧山嘉久: 遺伝性痙性対麻痺の最前線の概略. 難病と在宅ケア 24: 5, 2018.
  5. 瀧山嘉久: 遺伝性痙性対麻痺 (HSP) の病態とわが国における研究の現状. 特定非営利活動法人 全国脊髄小脳変性症 (SCD)・多系統萎縮症 (MSA) 友の会ニュース 234: 15-20, 2018.

＜著書＞

  1. 瀧山嘉久: 脊髄小脳変性症・多系統萎縮症診療ガイドライン2018, 監修　日本神経学会・厚生労働省「運動失調症の医療基盤に関する調査研究班」, 編集「脊髄小脳変性症・多系統萎縮症診療ガイドライン」作成委員会. 南江堂: 95-117, 222-235, 2018.
  2. 瀧山嘉久: 口部ジスキネジー, 今日の治療指針 私はこう治療している, 福井次矢ら 編. 医学書院: 945-946, 2018.
  3. 瀧山嘉久: 痙性対麻痺, 神経変性疾患ハンドブック-神経難病へのエキスパートアプローチ, 水澤英洋編. 南江堂: 237-251, 2018.
  4. 瀧山嘉久: bacrofen髄注療法, 神経疾患最新の治療 2018-2020, 水澤英洋ら編. 南江堂: 74-76, 2018.
  5. 脊髄小脳変性症・多系統萎縮症診療ガイドライン2018　遺伝性痙性対麻痺, 症状改善治療. 南江堂: 2018.

2017年

＜論文＞

  1. Yamashiro K, Tanaka R, Urabe T, Ueno Y, Yamashiro Y, Nomoto K, Takahashi T, Tsuji H, Asahara T and Hattori N: Gut dysbiosis is associated with metabolism and systemic inflammation in patients with ischemic stroke. PLoS One, 12:e0171521, 2017.
  2. Taniguchi D, Oji Y, Ueno Y, Hirayama S, Fukui M, Miyamoto N, Yamashiro K, Tanaka R, Suzuki K and Hattori N: Limb-Shaking Transient Ischemic Attack Induced by Middle Cerebral Artery Dissection after Lung Surgery. J Stroke Cerebrovasc Dis, 26:e197-e198, 2017.
  3. Miyamoto N, Tanaka R, Ueno Y, Watanabe M, Kurita N, Hira K, Shimada Y, Kuroki T, Yamashiro K, Urabe T and Hattori N: Analysis of the Usefulness of the WORSEN Score for Predicting the Deterioration of Acute Ischemic Stroke. J Stroke Cerebrovasc Dis, 26:2834-2839, 2017.
  4. Kamakura CK, Ueno Y, Sakai Y, Yoshida H, Aiba S, Hayashi A, Shimura H, Takeda K, Kamakura K, Hattori N and Urabe T: White matter lesions and cognitive impairment may be related to recovery from unilateral spatial neglect after stroke. J Neurol Sci, 379:241-246, 2017.
  5. Fukuda R, Miyamoto N, Hayashida A, Ueno Y, Yamashiro K, Tanaka R and Hattori N: Acute Hearing Loss Caused by Decreasing Anterior Inferior Cerebellar Arterial Perfusion in a Patient with Vertebral Artery Stenosis. J Stroke Cerebrovasc Dis, 26:e119-e121, 2017.
  6. Hasegawa A, Koike R, Koh K, Kawakami A, Hara N, Takiyama Y, and Ikeuchi T: Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family. J Neurol Sci 372: 128-130, 2017.
  7. Shindo K, Tsuchiya M, Ichinose Y, Koh K, Hata T, Yamashiro N, Kobayashi F, Nagasaka T, and Takiyama Y: Vasomotor regulation in patients with multiple system atrophy. J Neural Transm 124: 477-481, 2017.
  8. Shindo K, Tsuchiya M, Ichinose Y, Koh K, Hata T, Yamashiro N, Kobayashi F, Nagasaka T, and Takiyama Y: Pre- and postganglionic vasomotor dysfunction causes distal limb coldness in multiple system atrophy. J Neurol Sci 380: 191-195, 2017.
  9. Sato T, Natori T, Hata T, Yamashiro N, Shindo K, and Takiyama Y. Camptocormia as an onset symptom of myasthenia gravis. Neurol Sci 38: 515-516, 2017.
  10. 高橋祐二, 石川欽也, 宇川義一, 吉良潤一, 桑原　聰, 佐々木秀直, 祖父江　元, 高嶋　博, 瀧山嘉久, 辻　省次, 中島健二, 小野寺　理, 吉田邦広, 水澤英洋: 運動失調症患者登録・自然歴調査J-CAT. 厚生労働科学研究費補助金 (難治性疾患等政策研究事業) 運動失調症の医療基盤に関する調査研究 平成28年度総括・分担研究報告書: 27-29, 2017.
  11. 瀧山嘉久, 一瀬佑太, 高　紀信, 長坂高村, 新藤和雅, 石浦浩之, 辻　省次, JASPAC: 痙性対麻痺に対するITB療法の臨床評価項目の検討. 厚生労働科学研究費補助金 (難治性疾患等政策研究事業) 運動失調症の医療基盤に関する調査研究 平成28年度総括・分担研究報告書: 25-26, 2017.
  12. 羽田貴礼，土屋　舞，高　紀信，高木隆助，長坂高村，瀧山嘉久：II型呼吸不全を契機に診断された抗ミトコンドリア抗体陽性筋炎の1例. 山梨医学44：16-18, 2017.
  13. 高木隆助，長坂高村，諏訪裕美，土屋　舞，高　紀信，瀧山嘉久：反射性ミオクローヌスを認めたBickerstaff脳幹脳炎の1例. 臨床神経 57 : 395-398, 2017.
  14. 土屋　舞，高木隆助，小林史和，長坂高村，新藤和雅，瀧山嘉久：Fanconi症候群による多発性偽骨折を認めたWilson病の1例. 臨床神経 57 : 527-530, 2017.
  15. 名取高広，新藤和雅，土屋　舞，福元　恵，高木隆助，山城亘央，長坂高村，瀧山嘉久：脳卒中様エピソードを繰り返した成人型神経核内封入体病の1例. 山梨医科大学雑誌 32 : 105-110, 2017.

＜総説＞

  1. 新藤和雅, 瀧山嘉久: Cheyne-Stokes呼吸. Clinical Neuroscience 35: 729-731, 2017.
  2. 瀧山嘉久: 遺伝性痙性対麻痺のゲノム医療. 神経内科 86: 672-677, 2017.
  3. 瀧山嘉久: 遺伝性痙性対麻痺とその分類. Clinical Neuroscience 35: 1053-1056, 2017.
  4. 新藤和雅, 瀧山嘉久: 網様体の機能と病態　Cheyne-Stokes呼吸. Clinical Neuroscience 35: 729-731, 2017.

2016年

＜論文＞

  1. Ueno Y, Yamashiro K, Tanaka R, Kuroki T, Hira K, Kurita N, Urabe T and Hattori N: Emerging Risk Factors for Recurrent Vascular Events in Patients With Embolic Stroke of Undetermined Source. Stroke, 47:2714-2721, 2016.
  2. Ueno Y, Nakamura R and Hattori N: Reply to CLIPPERS features before, during and after lymphoma. J Neurol Sci, 366:253-254, 2016.
  3. Takeshige H, Ueno Y, Sasaki F, Namera A, Matsukawa T, Yokoyama K and Hattori N: Acute hippocampal and chronic diffuse white matter involvement in severe methanol intoxication. Neurology, 87:2382-2383, 2016.
  4. Takeshige H, Ueno Y, Kamagata K, Sasaki F, Yamashiro K, Tanaka R, Aoki S and Hattori N: Pathways Linked to Internuclear Ophthalmoplegia on Diffusion-Tensor Imaging in a Case with Midbrain Infarction. J Stroke Cerebrovasc Dis, 25:2575-2579, 2016.
  5. Nakamura R, Ueno Y, Ando J, Matsuda H, Masuda A, Iiduka K, Shingai N, Takanashi M, Yokoyama K, Komatsu N and Hattori N: Clinical and radiological CLIPPERS features after complete remission of peripheral T-cell lymphoma, not otherwise specified. J Neurol Sci, 364:6-8, 2016.
  6. Kuroki T, Tanaka R, Shimada Y, Yamashiro K, Ueno Y, Shimura H, Urabe T and Hattori N: Exendin-4 Inhibits Matrix Metalloproteinase-9 Activation and Reduces Infarct Growth After Focal Cerebral Ischemia in Hyperglycemic Mice. Stroke, 47:1328-1335, 2016.
  7. Shindo K, Miwa M, Kobayashi F, Nagasaka T, and Takiyama Y: Muscle sympathetic nerve activity in frontotemporal lobar degeneration is similar to ALS. Clin Auton Res 26: 1-5, 2016.
  8. Koh K, Tsuchiya M, Takaki R, Togashi S, Nagasaka T, Shindo K, and Takiyama Y: Huge brain cystic lesions resulting from metronidazole-induced encephalopathy. J Neurol Neurophysiol 7: 2016.
  9. Nakamura R, Sone J, Atsuｔa N, Tohnai G, Watanabe H, Yokoi D, Nakatochi M Watanabe H, Ito M, Katsuno F, Tanaka F, Li Y, Izumi Y, Morita M, Taniguchi A, Kano O, Oda M, Kuwabara S, Abe I, Okamoto K, Mizoguchi K, Hasegawa K, Aoki M, Hattori N, Tsuji S, Nakashima K, JaCALS, et al: Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort. Neurobiol Aging 39: 219, e1-e8, 2016.
  10. Sone J, Mori K, Inagaki T, Katsumata R, Takagi S, Yokoi S, Araki K, Kato T, Nakamura T, Koike H, Takashima H, Hashiguchi A, Kohno Y, Kurashige T, Kuriyama M, Takiyama Y, Tsuchiya M, Kitagawa N, Kawamoto M, Yoshimura H, Suto Y, Nakayasu H, Uehara N, Sugiyama H, Takahashi M, Kokubun N, Konno T, Katsuno M, Tanaka F, Iwasaki Y, Yoshida M, and Sobue G: Clinicopathological features of adult-onset neuronal intranuclear inclusion disease: a study of 57 cases. Brain 139: 3170-3186, 2016.
  11. Takiyama Y, Wang Y, Koh K, Ichinose Y, and Shindo K: A p.R464H variation in the CCDC88C gene may not cause a dominant form of spinocerebellar ataxia. J Med Genet (eLetters) [Published 10 October 2016]
  12. Shindo K, Tsuchiya M, Yamashiro N, Kobayashi F, Nagasaka T, and Takiyama Y: Changes of sympathetic thermoregulatory function with aging. Clin Auton Res 26 : 461-464, 2016.
  13. Ichinose Y, Koh K, Fukumoto M, Yamashiro N, Kobayashi F, Miwa M, Nagasaka T, Shindo K, Ishiura H, Tsuji S, and Takiyama Y. Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8. Clin Neurol Neurosurg 144: 36-38, 2016.
  14. Wang Y, Koh K, Takaki R, Shindo K, and Takiyama Y. Hot cross bun sign in a late-onset SCA1 patient. Neurol Sci 37: 1873-1874, 2016.
  15. Wang Y, Koh K, Ichinose Y, Yasumura M, Ohtsuka T, and Takiyama Y. A de novo mutation in the NALCN gene in an adult patient with cerebellar ataxia associated with intellectual disability and arthrogryposis. Clin Genet 96: 556-557, 2016.
  16. Shindo K, Onohara A, Hata T, Kobayashi F, Nagasaka K, Nagasaka T, and Takiyama Y: Opsoclonus-myoclonus syndrome associated with multiple system atrophy. Cerebellum & Ataxias 1: 15, 2014.
  17. 一瀬佑太, 三輪道然, 名取高広, 土屋　舞, 小野原亜希子, 高　紀信, 福元　恵, 高木隆助, 山城亘央, 小林史和, 長坂高村, 新藤和雅, 瀧山嘉久: 遺伝性痙性対麻痺における髄腔内バクロフェン療法の治療効果の検討. 山梨医学 43: 25-29, 2016.
  18. 名取高広, 福元　恵, 長坂高村, 小野原亜希子, 髙　紀信, 髙木隆助, 山城亘央, 小林史和, 新藤和雅, 瀧山嘉久: 当科におけるCreutzfeldt-Jakob病の臨床・分子遺伝学的検討.　山梨医学43: 30-34. 2016.
  19. 新村浩透，長坂高村，土屋　舞，小野原亜希子，高木隆助，瀧山嘉久：シェーグレン症候群に合併した急性辺縁系脳炎の1例. Brain Nerve 68：567-571, 2016
    20. 016

＜総説＞

  1. 新藤和雅, 瀧山嘉久：神経核内封入体病の臨床症状. 神経内科 85: 594-600. 2016.
  2. 瀧山嘉久: 変性疾患　遺伝性痙性対麻痺の現状. Annual Review 神経2016: 173-179, 2016.
  3. 瀧山嘉久: 最近わかった疾患　SCA36, SCA34. 難病と在宅ケア 22: 14-15, 2016.
  4. 瀧山嘉久: 感覚異常. 看護学生のための神経内科学テキスト. 中外医学社: 160-166, 2016.
  5. 瀧山嘉久: 視力・視野障害. 看護学生のための神経内科学テキスト. 中外医学社: 167-171, 2016.

＜著書＞

  1. 瀧山嘉久: 運動失調, 神経内科ハンドブック　鑑別診断と治療 (第5版), 水野美邦 編. 医学書院: 342-357, 2016.

2015年

＜論文＞

  1. Yatomi Y, Tanaka R, Shimada Y, Yamashiro K, Liu M, Mitome-Mishima Y, Miyamoto N, Ueno Y, Urabe T and Hattori N: Type 2 diabetes reduces the proliferation and survival of oligodendrocyte progenitor cells in ishchemic white matter lesions. Neuroscience, 289:214-223, 2015.
  2. Ueno Y, Yamashiro K, Tanaka Y, Watanabe M, Miyamoto N, Shimada Y, Kuroki T, Tanaka R, Miyauchi K, Daida H, Hattori N and Urabe T: Rosuvastatin may stabilize atherosclerotic aortic plaque: transesophageal echocardiographic study in the EPISTEME trial. Atherosclerosis, 239:476-482, 2015.
  3. Ueno Y, Tanaka R, Yamashiro K, Shimada Y, Kuroki T, Hira K, Urabe T and Hattori N: Impact of BNP on cryptogenic stroke without potential embolic sources on transesophageal echocardiography. J Neurol Sci, 359:287-292, 2015.
  4. Ueno Y, Koike M, Shimada Y, Shimura H, Hira K, Tanaka R, Uchiyama Y, Hattori N and Urabe T: L-carnitine enhances axonal plasticity and improves white-matter lesions after chronic hypoperfusion in rat brain. J Cereb Blood Flow Metab, 35:382-391, 2015.
  5. Ueno S, Miyamoto N, Shimura H, Ueno Y, Watanabe M, Hayashi A, Hattori N and Urabe T: Successful immune moderation treatment for progressive encephalomyelitis with rigidity and myoclonus. Intern Med, 54:219-221, 2015.
  6. Tanaka Y, Ueno Y, Shimada Y, Yamashiro K, Tanaka R, Urabe T and Hattori N: Paradoxical brain embolism associated with Kimura disease mimics watershed infarction. J Stroke Cerebrovasc Dis, 24:e55-57, 2015.
  7. Tanaka R, Yamashiro K, Okuma Y, Shimura H, Nakamura S, Ueno Y, Tanaka Y, Miyamoto N, Tomizawa Y, Nakahara T, Furukawa Y, Watada H, Kawamori R, Hattori N and Urabe T: Effects of Pioglitazone for Secondary Stroke Prevention in Patients with Impaired Glucose Tolerance and Newly Diagnosed Diabetes: The J-SPIRIT Study. J Atheroscler Thromb, 22:1305-1316, 2015.
  8. Kobayashi M, Tanaka R, Yamashiro K, Ueno Y, Kato E, Miura S, Daida H and Hattori N: Pre-existing Mobile Cardiac Thrombus and the Risk of Early Recurrent Embolism after Intravenous Thrombolysis: A Case Report. J Stroke Cerebrovasc Dis, 24:e161-163, 2015.
  9. Hosomi N, Nagai Y, Kohriyama T, Ohtsuki T, Aoki S, Nezu T, Maruyama H, Sunami N, Yokota C, Kitagawa K, Terayama Y, Takagi M, Ibayashi S, Nakamura M, Origasa H, Fukushima M, Mori E, Minematsu K, Uchiyama S, Shinohara Y, Yamaguchi T, Matsumoto M and Collaborators JS: The Japan Statin Treatment Against Recurrent Stroke (J-STARS): A Multicenter, Randomized, Open-label, Parallel-group Study. EBioMedicine, 2:1071-1078, 2015.
  10. Koh K, Kobayashi F, Miwa M, Shindo K, Isozaki E, Ishiura H, Tsuji S, and Takiyama Y: Novel mutations in the PNPLA6 gene in Boucher-Neuhauser syndrome. J Hum Genet 60: 217-220, 2015.
  11. Shindo K, Tsuchiya M, Ichinose Y, Onohara A, Fukumoto M, Koh K, Takaki R, Yamashiro N, Kobayashi F, Nagasaka T, and Takiyama Y. No relation between sympathetic outflow to muscles and respiratory function in amyotrophic lateral sclerosis. J Neurol Sci 358: 66-71, 2015.
  12. Wang Y, Koh K, Namekawa M, and Takiyama Y: Whole-exome sequencing reveals a missense mutation in the KCND3 gene in a patient with SCA19/22. Neurol Clin Neurosci 3: 197-199, 2015.
  13. Murata M, Hsegawa K, Kanazawa I, Fukasaka J, Kochi K, Shimazu R, and The Japan Zonisamide on PD Study Group. Zonisamide improves wearing-off in Parkinson’s disease: A randomized, double-blind study. Mov Disord 30: 1343-1350, 2015.
  14. Nagasaka T, Shindo K, and Takiyama Y: Thalamic and thalamic reticular abnormalities in a patient with 22q11.2 deletion syndrome. J Neuropsychiatry Clin Neurosci 27: e81-e2, 2015.
  15. Onohara A, Koh K, Nagasaka T, Shindo K, Kato M, Aoki M, and Takiyama Y: A Japanese ALS patient with learning disabilities with a deletion mutation in the C-terminal of the FUS/TLS gene. Neurol Clin Neurosci 3: 192-193, 2015.
  16. 山城亘央, 長坂高村, 高木隆助, 三輪道然, 新藤和雅, 瀧山嘉久：緩徐進行性の歩行障害と記銘力低下で発症したクリプトコッカス脳室炎の1例. 臨床神経55：81-86, 2015.
  17. 小野原亜希子, 長坂高村, 土屋　舞, 高木隆助, 山城亘央, 新村透浩, 新藤和雅, 瀧山嘉久：Opsoclonus-myoclonus syndromeを呈した1例. 山梨医学42：31-33, 2015.
  18. 福元　恵, 一瀬佑太, 高木隆助, 小林史和, 新藤和雅, 瀧山嘉久：感覚性運動失調を主症状とした慢性炎症性脱髄性多発ニューロパチーの1例. 山梨医学42：28-30, 2015.
  19. 高木隆助, 長坂高村, 新藤和雅, 桐戸敬太, 瀧山嘉久：長期寛解後腕神経叢に再発を認めたneurolymphomatosisの1例. 神経内科82：223-227, 2015.
  20. 高　紀信, 高木隆助, 三輪道然, 長坂高村, 新藤和雅, 瀧山嘉久：プリオン蛋白遺伝子のコドン180と232にdouble mutationを認めたCreutzfeldt-Jakob病の1例. 臨床神経55：424-427, 2015.
  21. 山城亘央, 長坂高村, 高木隆助, 三輪道然, 新藤和雅, 瀧山嘉久：緩徐進行性の歩行障害と記銘力低下で発症したクリプトコッカス脳室炎の1例. 臨床神経 55 : 81-86, 2015.
  22. 小野原亜希子, 長坂高村, 土屋　舞, 高木隆助, 山城亘央, 新村透浩, 新藤和雅, 瀧山嘉久：Opsoclonus-myoclonus syndromeを呈した1例. 山梨医学 42 : 31-33, 2015.
  23. 山城亘央, 長坂高村, 富樫慎治, 新藤和雅, 瀧山嘉久: シロスタゾール単独投与により高度脳底動脈狹窄の改善を認めた1例. 神経内科 82 : 635-637, 2015.

＜総説＞

  1. Nagasaka T and Takiyama Y: Home- and community-based medical care for neurodegenerative diseases: ALS as an illustration. In: Ed. Wada K, editor. Neurodegenerative Disorders as Systemic Diseases. Tokyo Springer: 237-275, 2015.
  2. 新藤和雅, 瀧山嘉久: 感覚障害を呈する疾患の診断と治療：脊髄脊椎疾患. Clinical Neuroscience 33: 578-579, 2015.
  3. 布村明彦, 菅沼真由美, 新藤和雅, 瀧山嘉久：山梨認知症を考える会「認知症サポート医」の支援にフォーカスを絞って. 日本早期認知症学会誌 8: 104-107, 2015.
  4. 瀧山嘉久: 血管性認知症と混合型認知症. 日本早期認知症学会誌 8: 120-122, 2015.
  5. 瀧山嘉久: 前頭側頭型認知症. 日本早期認知症学会誌 8: 123-125, 2015.
  6. 瀧山嘉久: NBIA最近の進歩BPANとneuroferritinopathyを中心に. MDSJ Letters 8: 4-7, 2015.
  7. 瀧山嘉久: 小脳の病態　小脳疾患診の最前線　遺伝性痙性対麻痺. 医学のあゆみ 255: 1055-1061, 2015.

＜著書＞

  1. 瀧山嘉久: 本態性振戦, 今日の治療指針：私はこう治療している 2015, 山口　徹ら編. 医学書院: 903-904, 2015.
  2. 瀧山嘉久: Sturge-Weber症候群. 今日の診断指針　第7版, 金澤一郎・永井良三編. 医学書院: 601-602, 2015.

2014年

＜論文＞

  1. Yamashiro K, Tanaka R, Tanaka Y, Miyamoto N, Shimada Y, Ueno Y, Urabe T and Hattori N: Visceral fat accumulation is associated with cerebral small vessel disease. Eur J Neurol, 21:667-673, 2014.
  2. Yamashiro K, Tanaka R, Okuma Y, Ueno Y, Tanaka Y, Hattori N and Urabe T: Associations of durations of antiplatelet use and vascular risk factors with the presence of cerebral microbleeds. J Stroke Cerebrovasc Dis, 23:433-440, 2014.
  3. Yamashiro K, Tanaka R, Okuma Y, Shimura H, Ueno Y, Miyamoto N, Urabe T and Hattori N: Cerebral microbleeds are associated with worse cognitive function in the nondemented elderly with small vessel disease. Cerebrovasc Dis Extra, 4:212-220, 2014.
  4. Ueno Y, Yamashiro K, Tanaka Y, Watanabe M, Shimada Y, Kuroki T, Miyamoto N, Daimon M, Tanaka R, Miyauchi K, Daida H, Hattori N and Urabe T: Rationale and design of the EPISTEME trial: efficacy of post-stroke intensive rosuvastatin treatment for aortogenic embolic stroke. Cardiovasc Drugs Ther, 28:79-85, 2014.
  5. Ueno Y, Okuzumi A, Watanabe M, Tanaka Y, Shimada Y, Yamashiro K, Tanaka R, Hattori N and Urabe T: Cerebral small artery diseases may be associated with aortic arch calcification in stroke patients. J Atheroscler Thromb, 21:1011-1021, 2014.
  6. Mori A, Ueno Y, Kuroki T, Hoshino Y, Shimura H, Sekiguchi Y, Noguchi M, Hamada Y, Kusunoki S, Hattori N and Urabe T: Motor-dominant polyneuropathy due to IgM monoclonal antibody against disialosyl gangliosides in a patient with mantle cell lymphoma. J Neurol Sci, 337:215-218, 2014.
  7. Kurita N, Ueno Y, Watanabe M, Miyamoto N, Shimura H, Nonaka S, Tsutsumi S, Yasumoto Y, Hattori N and Urabe T: Three cases of cervicocephalic artery dissection in an amusement park. J Stroke Cerebrovasc Dis, 23:e467-471, 2014.
  8. Amano H, Miyamoto N, Shimura H, Sato DK, Fujihara K, Ueno S, Nakamura R, Ueno Y, Watanabe M, Hattori N and Urabe T: Influenza-associated MOG antibody-positive longitudinally extensive transverse myelitis: a case report. BMC Neurol, 14:224, 2014.
  9. Shindo K, Kobayashi F, Miwa M, Nagasaka T, Takiyama Y, Shiozawa Z: Active vasodilation by sympathetic outflow to limb skin in a patient with progressive aphasia.Neuroreport 25:303-306, 2014.
  10. Ichinose Y, Miwa M, Onohara A, Obi K, Shindo K, Saitsu H, Matsumoto N, Takiyama Y: Characteristic MRI findings in beta-propeller protein-associated neurodegeneration (BPAN). Neurol Clin Pract 4: 175-177, 2014.
  11. Shimazaki H, Honda J, Naoi T, Namekawa M, Nakano I, Yazaki Y, Nakamura K, Yoshida K, Ikeda S, Ishiura H, Fukuda Y, Takahashi Y, Goto J, Tsuji S, and Takiyama Y: Autosomal recessive complicated spastic paraplegia with lysosomal trafficking regulator gene mutation. J Neurol Neurosurg Psychiatry 85: 1024-1028, 2014.
  12. Koh K, Ishiura H, Miwa M, Doi K, Yoshimura J, Mitsui J, Goto J, Morishita S, Tsuji S, and Takiyama Y: Exome sequencing reveals a novel de novo mutation in ATL1. Neurol Clin Neurosci 2: 1-4, 2014.
  13. Wang Y, Koh K, Miwa M, Shindo K, and Takiyama Y: A Japanese SCA5 family with a novel 3-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study. J Hum Genet 59: 569-573, 2014.
  14. Shindo K, Kobayashi F, Miwa M, Nagasaka T, Takiyama Y, Shiozawa Z. Active vasodilation by sympathetic outflow to limb skin in a patient with progressive aphasia. NeuroReport 25: 303-6, 2014.
  15. Ichinose Y, Miwa M, Onohara A, Obi K, Shindo K, Saitsu H, Matsumoto N, and TakiyamaY: Characteristic MRI findings in beta-propeller protein-associated neurodegeneration (BPAN). Neurology: Clinical Practice 4: 175-177, 2014.
  16. Shindo K, Onohara A, Hata T, Kobayashi F, Nagasaka K, Nagasaka T, and Takiyama Y: Opsoclonus-myoclonus syndrome associated with multiple system atrophy. Cerebellum & Ataxias 1: 15, 2014.

＜総説＞

  1. 長坂高村, 瀧山嘉久：クリプトコッカス髄膜脳炎, 最新医学　別冊　新しい診断と治療のABC 82 神経関連感染症 水澤英洋編. 最新医学: 226-234, 2014.
  2. 瀧山嘉久: 連載「病態解明・新規治療を目指した神経疾患の患者レジストリウムシステム」痙性対麻痺: JASPAC. BRAIN NERVE 66: 1210-1217, 2014.
  3. 瀧山嘉久: 本邦の痙性対麻痺に関する全国多施設共同研究体制 (JASPAC). 脊椎脊髄ジャーナル 27: 737-745, 2014.
  4. 瀧山嘉久: 遺伝性痙性対麻痺の最新情報.　臨床神経学 54: 1009-1011, 2014.

＜著書＞

  1. 瀧山嘉久: 症候からみる神経内科 診断のコツ 治療のポイント, 鈴木則宏編(書評): 2014.
  2. 瀧山嘉久: 変性疾患 脊髄小脳変性症 劣性遺伝性脊髄小脳変性症 シャルルヴォア・サグネ型劣性遺伝性痙性失調症 神経症候群II , 水澤英洋編. 日本臨床: 397-401, 2014.
  3. 三輪道然, 瀧山嘉久: 変性疾患 脊髄小脳変性症 劣性遺伝性脊髄小脳変性症　SCAR8 (ARCA-1), 神経症候群II , 水澤英洋編. 日本臨床: 405-407, 2014.
  4. 太田恵美子, 瀧山嘉久: 変性疾患 錐体外路系疾患 不随性運動を主とする疾患 脳内鉄沈着を伴う神経変性症 神経フェリチン症 (Neuroferritinopathy), 神経症候群II, 水澤英洋編. 日本臨床: 297-301, 2014.
  5. 瀧山嘉久: 変性疾患, 脊髄小脳変性症　遺伝性痙性対麻痺　遺伝性痙性対麻痺概論, 神経症候群II , 水澤英洋編. 日本臨床: 417-422, 2014.
  6. 瀧山嘉久: 遺伝性痙性対麻痺, 神経内科研修ノート, 鈴木則宏編. 診断と治療: 300-302, 2014
  7. 瀧山嘉久: シャルルヴォア・サグネ型痙性失調症.　神経症候群（第2版） 別冊日本臨床社: 397-380, 2014.

2013年

＜論文＞

  1. Zhang Y, Ueno Y, Liu XS, Buller B, Wang X, Chopp M and Zhang ZG: The MicroRNA-17-92 cluster enhances axonal outgrowth in embryonic cortical neurons. J Neurosci, 33:6885-6894, 2013.
  2. Ueno Y, Watanabe M, Tanaka Y, Kuroki T, Kurita N, Shimura H, Hattori N and Urabe T: Temporal changes of ulcerative plaques in the aortic arch in recurrent stroke patients. J Stroke Cerebrovasc Dis, 22:e597-601, 2013.
  3. Tanaka Y, Ueno Y, Miyamoto N, Shimada Y, Tanaka R, Hattori N and Urabe T: Patent foramen ovale and atrial septal aneurysm can cause ischemic stroke in patients with antiphospholipid syndrome. J Neurol, 260:189-196, 2013.
  4. Tanaka R, Ueno Y, Miyamoto N, Yamashiro K, Tanaka Y, Shimura H, Hattori N and Urabe T: Impact of diabetes and prediabetes on the short-term prognosis in patients with acute ischemic stroke. J Neurol Sci, 332:45-50, 2013.
  5. Shimada Y, Ueno Y, Tanaka Y, Okuzumi A, Miyamoto N, Yamashiro K, Tanaka R, Hattori N and Urabe T: Aging, aortic arch calcification, and multiple brain infarcts are associated with aortogenic brain embolism. Cerebrovasc Dis, 35:282-290, 2013.
  6. Okuzumi A, Ueno Y, Shimada Y, Tanaka Y, Miyamoto N, Yamashiro K, Tanaka R, Hattori N and Urabe T: Impact of low-density lipoprotein to high-density lipoprotein ratio on aortic arch atherosclerosis in unexplained stroke. J Neurol Sci, 326:83-88, 2013.
  7. Nakajima A, Ueno Y, Shimura H, Kambe T, Nishioka K, Hattori N and Urabe T: Acute transient freezing of gait in a patient with posterior reversible encephalopathy syndrome. BMC Neurol, 13:79, 2013.
  8. Miyamoto N, Tanaka Y, Ueno Y, Kawamura M, Shimada Y, Tanaka R, Hattori N and Urabe T: Demographic, clinical, and radiologic predictors of neurologic deterioration in patients with acute ischemic stroke. J Stroke Cerebrovasc Dis, 22:205-210, 2013.
  9. Kuroki T, Ueno Y, Takeda I, Kambe T, Nishioka K, Shimura H, Itoh M, Hattori N and Urabe T: Recurrent embolic strokes associated with vertical atlantoaxial subluxation in a patient with rheumatoid arthritis: a case report and review of literature. J Stroke Cerebrovasc Dis, 22:e676-681, 2013.
  10. Kambe T, Shimura H, Ueno Y, Nishioka K, Tanaka R, Hattori N and Urabe T: Vivid visual hallucinations manifested as the initial symptom in a patient with neurosyphilis. Psychosomatics, 54:284-285, 2013.
  11. Hoshino Y, Ueno Y, Shimura H, Miyamoto N, Watanabe M, Hattori N and Urabe T: Marchiafava-Bignami disease mimics motor neuron disease: case report. BMC Neurol, 13:208, 2013.
  12. Fozouni N, Chopp M, Nejad-Davarani SP, Zhang ZG, Lehman NL, Gu S, Ueno Y, Lu M, Ding G, Li L, Hu J, Bagher-Ebadian H, Hearshen D and Jiang Q: Characterizing brain structures and remodeling after TBI based on information content, diffusion entropy. PLoS One, 8:e76343, 2013.
  13. Shimazaki H, Takiyama Y, Honda J, Sakoe K, Namekawa M, Tsugawa J, Tsuboi Y, Suzuki C, Baba M, Nakano I: Middle cerebellar peduncles and pontine T2 hypointensities in ARSACS. J Neuroimaging 23: 82-85, 2013.
  14. Furusawa Y, Mukai Y, Kawazoe T, Sano T, Nakamura H, Sakamoto C, Iwata Y, Wakita M, Nakata Y, Kamiya K, Kobayashi Y, Sakamoto T, Takiyama Y, Murata M: Long-term effect of repeated lidocaine injections into the external oblique for upper camptocormia in Parkinson’s disease. Parkinsonism Relat Disord 19: 350-354, 2013.
  15. Shindo K, kobayashi F, Miwa M, Nagasaka T, Takiyama Y, Shiozawa Z: Temporal prolongation of decreased skin blood flow causes cold limbs in Parkinson’s disease. J Neural Transm 120: 445-451, 2013.
  16. Tetsuka S, Tominaga K, Ohta E, Kuroiwa K, Sakashita E, Kasashima K, Hamamoto T, Namekawa M, Morita M, Natsui S, Morita T, Tanaka K, Takiyama Y, Nakano I, Endo H: Paraneoplastic cerebellar degeneration associated with an onconeural antibody against creatine kinase, brain-type. J Neurol Sci 335: 48-57, 2013.
  17. 三輪道然, 高　紀信, 植松晶子, 羽田貴礼, 一瀬佑太, 小野原亜希子, 福元　恵, 高木隆助, 山城亘央, 小林史和, 長坂高村, 新藤和雅, 瀧山嘉久: 山梨大学神経内科における遺伝性痙性対麻痺の臨床・分子遺伝学的検討. 山梨医学 41: 48-51, 2013.
  18. 福元　恵，山城亘央，小林史和，長坂高村，瀧山嘉久：緑茶抽出物飲料の過剰摂取により低カリウム血症ミオパチーをきたした1例. 臨床神経 53 : 239-242, 2013.
  19. 高　紀信，長坂高村，小林史和，山城亘央，新藤和雅，瀧山嘉久：経過中に中枢性無呼吸を呈したクロイツフェルト・ヤコブ病の1例. 臨床神経 53 : 642-645, 2013.
  20. 土屋　舞，三輪道然，長坂高村，新藤和雅，瀧山嘉久：免疫グロブリン大量静注療法が有効であった慢性特発性失調型ニューロパチーの2例. 山梨医学 41 : 44-47, 2013.
  21. 一瀬佑太，山城亘央，高木隆助，長坂高村，瀧山嘉久：関節リウマチの治療中に発症したトキソプラズマ脳炎の一例. 山梨医学 41 : 40-43, 2013.

＜著書＞

  1. 瀧山嘉久: 痙性対麻痺 (HAMを含む), 今日の治療指針, 私はこう治療している, 山口　徹ら編. 医学書院: 817-818, 2013.
  2. 瀧山嘉久: 小脳障害を伴う遺伝性痙性対麻痺, アクチュアル脳・神経疾患の臨床　小脳と運動失調, 小脳は何をしているのか, 辻　省次・西澤正豊編. 中山書店: 215-221, 2013.
  3. 瀧山嘉久: 急性運動失調, 今日の臨床サポート. エルゼビア・ジャパン: 2013.

2012年

＜論文＞

  1. Yamashiro K, Tanaka R, Nishioka K, Ueno Y, Shimura H, Okuma Y, Hattori N and Urabe T: Cerebral infarcts associated with adenomyosis among middle-aged women. J Stroke Cerebrovasc Dis, 21:910 e911-915, 2012.
  2. Ueno Y, Chopp M, Zhang L, Buller B, Liu Z, Lehman NL, Liu XS, Zhang Y, Roberts C and Zhang ZG: Axonal outgrowth and dendritic plasticity in the cortical peri-infarct area after experimental stroke. Stroke, 43:2221-2228, 2012.
  3. Tanaka R, Kawanabe T, Yamauchi Y, Shimura H, Tanaka Y, Miyamoto N, Ueno Y, Urabe T, Hattori N and Tanaka S: Economy class stroke syndrome after a long drive. J Stroke Cerebrovasc Dis, 21:155-157, 2012.
  4. Shimada Y, Yoritaka A, Tanaka Y, Miyamoto N, Ueno Y, Hattori N and Takao U: Cerebral infarction in a young man using high-dose anabolic steroids. J Stroke Cerebrovasc Dis, 21:906 e909-911, 2012.
  5. Miyamoto N, Tanaka Y, Ueno Y, Tanaka R, Hattori N and Urabe T: Benefits of prestroke use of angiotensin type 1 receptor blockers on ischemic stroke severity. J Stroke Cerebrovasc Dis, 21:363-368, 2012.
  6. Cui X, Chopp M, Shehadah A, Zacharek A, Kuzmin-Nichols N, Sanberg CD, Dai J, Zhang C, Ueno Y, Roberts C and Chen J: Therapeutic benefit of treatment of stroke with simvastatin and human umbilical cord blood cells: neurogenesis, synaptic plasticity, and axon growth. Cell Transplant, 21:845-856, 2012.
  7. Buller B, Chopp M, Ueno Y, Zhang L, Zhang RL, Morris D, Zhang Y and Zhang ZG: Regulation of serum response factor by miRNA-200 and miRNA-9 modulates oligodendrocyte progenitor cell differentiation. Glia, 60:1906-1914, 2012.
  8. Shimazaki H, Takiyama Y: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects. Spinocerebellar Ataxia 155-172, 2012.
  9. Haga R, Miki Y, Funamizu Y, Kon T, Suzuki C, Ueno T, Nishijima H, Arai A, Tomiyama M, Shimazaki H, Takiyama Y, Baba M: Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay. Clin Neurol Neurosurg 114: 746-747, 2012.
  10. Namekawa M, Takiyama Y, Honda J, Sakoe K, Naoi T, Shimazaki H, Yamagata T, Momoi MY, Nakano I: A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy. Neurol Sci 33: 1389-1392, 2012.
  11. Shimazaki H, Takiyama Y, Ishiura H, Sakai C, Matsushima Y, Hatakeyama H, Honda J, Sakoe K, Naoi T, Namekawa M, Fukuda Y, Takahashi Y, Goto J, Tsuji S, Goyo Y, Nakanao I, JASPAC: A homozugous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55). J Med Genet 49; 777-784, 2012.
  12. Namekawa M, Takiyama Y, Honda J, Sakoe K, Naoi T, Shimazaki H, Yamagata T, Momoi M, Nakano I: A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy. Neurol Sci 33: 1389-1392, 2012.
  13. Ohta E, Takiyama Y: MRI findings in neuroferritinopathy. Neurol Res Int 2012.
  14. 松沢美幸, 安藤典子, 原田和俊, 川村龍吉, 柴垣直孝, 島田眞路, 長坂高村, 瀧山嘉久: 髄膜炎を合併した帯状疱疹の１例. 皮膚科の臨床54: 1786-1787, 2012.
  15. 三輪道然，中村由紀，長坂高村，新藤和雅，瀧山嘉久：筋萎縮が頚筋と上肢帯にほぼ限局して認められた抗SRP抗体陽性多発筋炎の 1例. 臨床神経 52 : 234-238, 2012.
  16. 羽田貴礼，高　紀信，小林史和，中村由紀，長坂高村，瀧山嘉久：腱反射亢進を認めたGuillain-Barré症候群の1例. 山梨医学40：35-37, 2012
  17. 一瀬佑太，高木隆助，三輪道然，新藤和雅，瀧山嘉久：慢性進行性の小脳性運動失調と薬剤性ミオパチーを合併したベーチェット病の1例. 山梨医学40：43-46, 2012.

＜著書＞

  1. Shimazaki H and Takiyama Y: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects. Spinocerebellar Araxia Editea byGazulla: 155-172, 2012.
  2. Ohta E and Takiyama Y: MRI findings in neuroferritinopathy. Neurology Research International 2012: 2012.
  3. 瀧山嘉久: 常染色体劣勢遺伝性SCD　シャルルヴォア・サグネ型痙性失（ARSACS).　最新医学 67: 1144-1149, 2012.
  4. 瀧山嘉久, 布村明彦：住み慣れた地域で誰もがいきいきと暮らせる街づくり（第4回）共に学び変化しながら「認知症になっても安心して暮らせる待ちづくり」を. クリニシアン59: 796-804, 2012.
  5. 瀧山嘉久: 山梨認知症を考える会, 共に学び認知症になっても安心して暮らせる街づくりを目指す. ぽ〜れぽ〜れ 386: 3, 2012.

2011年

＜論文＞

  1. Nagasaka T, Nagasaka K, Ohta E, Shindo K, Takiyama Y, Shiozawa Z, Miyazawa N, Yamasaki N, Mori N, Onda H, Shinohara T: Cerebral hypermetabolism demonstrated by FDG-PET in familial Creutzfeldt-Jakob disease. Clin Nucl Med 36: 725-727, 2011.
  2. Prust M, Wang J, Morizono H, Messing A, Brenner M, Gordon E, Hartka T, Sokohl A, Schiffmann R, Gordish-Dressman H, Albin R, Amartino H, Brockman K, Dinopoulos A, Dotti MT, Fain D, Fernandez R, Ferreira J, Fleming J, Gill D, Griebel M, Heilstedt H, Kaplan P, Lewis D, Nakagawa M, Pedersen R, Alyssa R, Sawaishi Y, Schneider M, Sherr E, Takiyama Y, Wakabayashi K, Gorospe JR, Vanderver A: GFAP mutations, age of onset and clinical subtypes in Alexander disease. Neurology 77: 1287-1294, 2011.
  3. Shindo K, Watanabe H, Ohta E, Nagasaka T, Shiozawa Z, Takiyama Y: Sympathetic sudomotor neural function in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 12: 39-44, 2011.
  4. 小野原亜希子，小林史和，中村由紀，長坂高村，新藤和雅，瀧山嘉久：単純ヘルペス脳炎類似の頭部MRI所見を認めた神経梅毒の1例. 神経内科 74 : 105-106, 2011.
  5. 瀧山嘉久, 石浦浩之, 嶋崎晴雄, 辻　省次, 西澤正豊: 遺伝性痙性対麻痺の疫学. 神経内科 74: 141-145, 2011.

＜著書＞

  1. 瀧山嘉久: 皮質性小脳萎縮症. 難病と在宅ケア 16: 47-49, 2011.
  2. 新藤和雅, 瀧山嘉久: 認知機能正常の高齢者におけるアルツハイマー病の生物学的マーカーと運動の関係. Cognition and Dementia 10: 60-61, 2011.
  3. 長坂高村, 瀧山嘉久: Gamma-secretase activating proteinはアルツハイマー病の治療ターゲットである. Cognition and Dementia 10: 62-63, 2011.
  4. 瀧山嘉久: わが国における遺伝性痙性対麻痺の現状. 臨床神経 51: 1125-1128, 2011.

2010年

＜論文＞

  1. Ueno Y, Shimada Y, Tanaka R, Miyamoto N, Tanaka Y, Hattori N and Urabe T: Patent foramen ovale with atrial septal aneurysm may contribute to white matter lesions in stroke patients. Cerebrovasc Dis, 30:15-22, 2010.
  2. Miyamoto N, Tanaka Y, Ueno Y, Tanaka R, Hattori N and Urabe T: Comparison of clinical backgrounds with anterior versus posterior circulation infarcts. J Stroke Cerebrovasc Dis, 19:393-397, 2010.
  3. Shindo K, Nagasaka T, Shiozawa Z, Takiyama Y: A case of recurrent polymyalgia rheumatica-like complications with pregnancy. Rheumatol Int 30: 541-542, 2010.
  4. Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I: Adult-onset Alexander disease with typical “tadpole” brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature. BMC Neurol 10: 21,2010.
  5. 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, Tsuji S, Hasegawa K, Shimohata T, Nishizawa M, Miyajima H, Kanda F, Watanabe Y, Nakashima K, Tsujino A, Yamashita T, Uchino M, Fujimoto Y, Tanaka F, Sobue G; Japan SBMA Interventional Trial for TAP-144-SR (JASMITT) study group. Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial.Lancet Neurol 9: 875-884, 2010.
  6. Shindo K, Nagasaka T, Shiozawa Z, Takiyama Y: A case of recurrent polymyalgia rheumatica-like complications with pregnancy. Rheumatol Int 30: 541-542, 2010.
  7. Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I: Adult-onset Alexander disease with typical “tadpole” brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature. BMC Neurology 10: 21, 2010.
  8. Nagasaka K, Ohta E, Nagasaka T, Togashi S, Miwa M, Nakamura Y, Shindo K, Shiozawa Z: Rhythmic pupillary oscillation in Creutzfeldt-Jakob disease associated with the Glu/Lys mutation of prion protein codon 200. Mov Disord 25: 111-6, 2010.
  9. 小林史和，栗原　康，長坂加織，飯田晴康，新藤和雅，瀧山嘉久：性腺機能低下症を合併した小脳性運動失調症の1例. 臨床神経 50 : 98-102, 2010.
  10. 金井真理，小林史和，三輪道然，中村由紀，長坂高村，新藤和雅，瀧山嘉久：左右交代性に再発した眼窩先端部症候群の1例. 山梨医学 38 : 182-184, 2010.

＜総説＞

  1. 瀧山嘉久, 石浦浩之, 嶋崎晴雄, 滑川道人, 高橋裕二, 後藤　順, 辻　省次, 西澤正豊: 神経疾患の臨床研究を目指したコンソーシアム　本邦の痙性対麻痺に関する全国多施設研究共同体制（JASPAC).　臨床神経学 50: 931-934, 2010.

＜著書＞

  1. 瀧山嘉久: 痙性脊髄麻痺, 今日の診断指針　第 6版, 金澤一郎・永井良三編. 医学書院: 615-617, 2010.

2009年

＜論文＞

  1. Urabe T, Watada H, Okuma Y, Tanaka R, Ueno Y, Miyamoto N, Tanaka Y, Hattori N and Kawamori R: Prevalence of abnormal glucose metabolism and insulin resistance among subtypes of ischemic stroke in Japanese patients. Stroke, 40:1289-1295, 2009.
  2. Ueno Y, Zhang N, Miyamoto N, Tanaka R, Hattori N and Urabe T: Edaravone attenuates white matter lesions through endothelial protection in a rat chronic hypoperfusion model. Neuroscience, 162:317-327, 2009.
  3. Saiki S, Ueno Y, Moritani T, Sato T, Sekine T, Kawajiri S, Adachi S, Yokoyama K, Tomizawa Y, Motoi Y and Hattori N: Extensive hemispheric lesions with radiological evidence of blood-brain barrier integrity in a patient with neuromyelitis optica. J Neurol Sci, 284:217-219, 2009.
  4. Saiki S, Sekine T, Ueno Y, Yoshino H, Takahashi J, Tani Y, Kambe Y, Motoi Y and Hattori N: [Adult-onset case of idiopathic neurodegeneration with brain iron accumulation without mutations in the PANK2 and PLA2G6 genes]. Rinsho Shinkeigaku, 49:474-478, 2009.
  5. 小林千尋，小林史和，長坂加織，飯田晴康，新藤和雅，瀧山嘉久：頭部MRIでてんかん重積による異常信号を呈した 1例. 山梨医学 37 : 183-187, 2009.

＜総説＞

  1. 太田恵美子, 長坂高村, 新藤和雅, 当間　忍, 長坂加織, 三輪道然, 瀧山嘉久, 塩澤全司：ニューロフェリチノパチーの臨床. 臨床神経 49: 254-261, 2009.
  2. 瀧山嘉久: 優性遺伝性家族性　MJD/SCA3. Clinical neuroscience, 27: 52-54, 2009.
  3. 瀧山嘉久: 遺伝性痙性対麻痺. 山梨医科学誌 24: 1-12, 2009.
  4. 瀧山嘉久: マチャド・ジョセフ病の臨床・分子遺伝学. 山梨医科学誌 24: 13-24, 2009.