業績リスト

2020年

<英文原著>
  1. Matsukawa T, Yamamoto T, Honda A, Toya T, Ishiura H, Mitsui J, Tanaka M, Hao A, Shinohara A, Ogura M, Kataoka K, Seo S, Kumano K, Hosoi M, Narukawa N, Yasunaga A, Maki H, Ichikawa M, Nannya Y, Imai Y, Takahashi T, Takahashi Y, Nagasako Y, Yasaka K, Mano KK, Matsukawa MK, Miyagawa T, Hamada M, Sakuishi K, Hayashi T, Iwata A, Terao Y, Shimizu J, Goto J, Mori M, Kunimatsu A, Aoki S, Hayashi S, Nakamura F, Arai S, Monma K, Ogata K, Yoshida T, Abe O, Inazawa J, Toda T, Kurokawa M and Tsuji S. Clinical efficacy of hematopoietic stem cell transplantation for adult adrenoleukodystrophy. Brain Communications. 2:fcz048, 2020. https://doi.org/10.1093/braincomms/fcz048.
  2. Yoshida M, Hayashi T, Fujii K, Ishiura H, Tsuji S and Sakurai Y. Selective impairment of On-reading (Chinese-style pronunciation) in alexia with agraphia forkanji due to subcortical hemorrhage in the left posterior middle temporal gyrus. Neurocase 2020. Online ahead of print. https://doi.org/10.1080/13554794.2020.1788608.
  3. Hongo H, Miyawaki S, Imai H, Shimizu M, Yagi S, Mitsui J, Ishiura H, Yoshimura J, Doi K, Qu W, Teranishi Y, Okano A, Ono H, Nakatomi H, Shimizu T, Morishita S, Tsuji S and Saito N. Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis. Sci Reports. (in press)
  4. Porto KJL, Matsukawa T, Ishiura H, Mitsui J, Matic A, Yu JM, Dominguez J, Damian L, Toda T and Tsuji S. A novel mutation in ABCD1 gene in a Filipino patient with Adult-Onset X-linked ALD. Neurol Clin Neurosci. 2020. Online ahead of print. https://doi.org/10.1111/ncn3.12425.
  5. Katoh K, Aiba K, Fukushi D, Yoshimura J, Suzuki Y, Mitsui J, Morishita S, Tuji S, Yamada K and Wakamatsu N. Clinical and molecular genetic characterization of two female patients harboring Xq27.3q28 deletion with different ratios of X chromosome inactivation. Human Mutation. 2020. Online ahead of print. https://doi.org/10.1002/humu.24058.
  6. Nakamura-Shindo K, Ono K, Koh K, Ishiura H and Tsuji S, Takiyama Y and Yamada M. A novel mutation in the GBA2 gene in a Japanese patient with SPG46: A case report. eNeurologicalSci. 19:100238, 2020. https://doi.org/10.1016/j.ensci.2020.100238.
  7. Uchino A, Nagai M, Kanazawa N, Ichinoe M, Yanagisawa N, Adachi K, Nanba E, Ishiura H, Mitsui J, Tsuji S, Suzuki K, Murayama S and Nishiyama K. An autopsy case of GM1 gangliosidosis type II in a patient who survived a long duration with artificial respiratory support. Neuropathology. 2020. Online ahead of print. https://doi.org/10.1111/neup.12651
  8. Lima S-Y, Ishiura H, Ramli N, Shibata S, Almansour MA, Tana AH, Houlden H, Lange AE and Tsuji S. Adult-onset neuronal intranuclear inclusion disease mimicking Fragile X-associated tremor-ataxia syndrome in ethnic Chinese patients. Parkinsonism & Related Disorders. 74:25-27, 2020. https://doi.org/10.1016/j.parkreldis.2020.03.025
  9. Ishihara S, Okamoto Y, Tanabe H, Yoshimura A, Higuchi Y, Yuan J-H, Hashiguchi A, Ishiura H, Mitsui J, Suwazono S, Oya Y, Sasaki M, Nakagawa M, Tsuji S, Ohya Y and Takashima H. Clinical features of inherited neuropathy with BSCL2 mutations in Japan. J Peripheral Nervous System. 25:125-131, 2020. https://doi.org/10.1111/jns.12369.
  10. Koh K, Ishiura H, Shimazaki H, Tsutsumiuchi M, Ichinose Y, Nan H, Hamada S, Ohtsuka T, Tsuji S and Takiyama Y. VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia. Mol Genet Genom Med. 8:e1108, 2020. https://doi.org/10.1002/mgg3.1108.
  11. Ueha R, Sato T, Goto T, Yamauchi A, Nativ-Zeltzer N, Mitsui J, Belafsky PC, Yamasoba T. Esophageal dysmotility is common in patients with multiple system atrophy. Laryngoscope. 2020. Online ahead of print. https://doi.org/10.1002/lary.28852.
  12. Nishizawa M, Onodera O, Hirakawa A, Shimizu Y, Yamada M; Rovatirelin Study Group (Tsuji S). Effect of rovatirelin in patients with cerebellar ataxia: two randomised double-blind placebo-controlled phase 3 trials. J Neurol Neurosurg Psychiatry. 91:254-262, 2020. http://doi.org/10.1136/jnnp-2019-322168.
  13. Kurosawa K, Tsuji S, Morishita S, Mitsui J, Ida K, Yokoi T, Tsurusaki Y, Abe-Hatano C, Enomoto Y and Naruto T. CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability. Eur J Med Genet 63:103610, 2020. https://doi.org/10.1016/j.ejmg.2018.12.015.
<英文総説>
  1. Ishiura H and Tsuji S. Advances in repeat expansion diseases and a new concept of repeat motif–phenotype correlation. Current Opinion in Genetics & Development (in press)
<和文総説>
  1. 三井 純.レジストリー研究の展望:MSA.科学評論社,脳神経内科 2020年3月 (2020; 92(3):276-279)
  2. 三井 純.シヌクレイノパチー:多系統萎縮症.医歯薬出版株式会社,医学のあゆみ 2020年4月 (2020;273:1)
<国際学会>
  1. Ueha R, Sato T, Goto T, Yamauchi A, Nativ-Zeltzer N, Mitsui J, Belafsky PC, Yamasoba T. Esophageal motility disorders are common in patients with multiple system atrophy. Combined Otolaryngology Spring Meetings 2020, Web, April 24th, 2020

2019年

<英文原著>
  1. Yasuda T, Matsukawa T, Mitsui J and Tsuji S. Oxygen consumption rate for evaluation of COQ2 variants associated with multiple system atrophy. Neurogenetics. 20:51-52, 2019. https://doi.org/10.1007/s10048-018-0563-7.
  2. Florian RT, Kraft F, Leitão E, Kaya S, Klebe S, Magnin E, van Rootselaar A-F, Buratti J, Kühnel T, Schröder C, Giesselmann S, Tschernoster N, Altmueller J, Lamiral A, Keren B, Nava C, Bouteiller D, Forlani V, Jornea L, Kubica R, Ye T, Plassard D, Jost B, Meyer V, Deleuze J-F, Delpu Y, Avarello MDM, Vijfhuizen LS, Rudolf G, Hirsch E, Kroes T, Reif1 PS, Rosenow F, Ganos C, Vidailhet M, Thivard L, Mathieu A, Bourgeron T, Kurth I, Rafehi H, Steenpass L, Horsthemke B, FAME consortium, LeGuern E Klein KM, Labauge P, Bennett MF, Bahlo M, Gecz J, Corbett MA, Tijssen MAJ, van den Maagdenberg AMJM, and Depienne C. 1,8,9 . FAME consortium: Berkovic SF, Bisulli F, Brancati F, Canafoglia L, Casari G, Guerrini R, Ishiura H, Licchetta L, Mei D, Pippucci T, Sadleir L, Scheffer IE, Striano P, Tinuper P, Tsuji S and Zara F. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with familial adult myoclonic epilepsy type 3. Nature Commun 10:4919, 2019. https://doi.org/10.1038/s41467-019-12763-9.
  3. Corbett MA, Kroes T, Veneziano L, Bennett MF, Florian R, Schneider AL, Coppola A, Licchetta L, Franceschetti S, Suppa A, Wenger A, Mei D, Pendziwiat M, Kaya S, Delledonne M, Straussberg R, Xumerle L, Regan B, Crompton D, van Rootselaar A-F, Correll A, Catford R, Bisulli F, Chakraborty S, Baldassari S, Tinuper P, Barton K, Carswell S, Smith M, Berardelli A, Carroll R, Gardner A, Friend KL, Blatt I, Iacomino M, Bonaventura CD, Striano S, Buratti J, Keren B, Nava C, Forlani S, Rudolf G, Hirsch E, Leguern E, Labauge P, Balestrini S, Sander JW, Afawi Z, Helbig I, Ishiura H, Tsuji S, Sisodiya SM, Casari G, Sadleir LG, van Coller R, Tijssen MAJ Klein KM, van den Maagdenberg AMJM, Zara F, Guerrini R, Berkovic SF, Pippucci T, Canafoglia L, Bahlo M, Striano P, Scheffer IE, Brancati F, Depienne C and Gecz J. Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2. Nature Commun 10:4920, 2019. https://doi.org/10.1038/s41467-019-12671.
  4. Ishiura H, Shibata S, Yoshimura J, Suzuki Y, Qu W, Doi K, Almansour MA, Kikuchi JK, Taira M, Mitsui J, Takahashi Y, Ichikawa Y, Mano T, Iwata A, Harigaya Y, Matsukawa MK, Matsukawa T, Tanaka M, Shirota Y, Ohtomo R, Kowa H, Date H, Mitsue A, Hatsuta H, Morimoto S, Murayama S, Shiio Y, Saito Y, Mitsutake A, Kawai M, Sasaki T, Sugiyama Y, Hamada M, Ohtomo G, Terao Y, Nakazato Y, Takeda A, Sakiyama Y, Umeda-Kameyama Y, Shinmi J, Ogata K, Kohno Y, Lim SY, Tan AH, Shimizu J, Goto J, Nishino I, Toda T, Morishita S and Tsuji S. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease. Nat Genet 51:1222-1232, 2019. https://doi.org/10.1038/s41588-019-0458-z.
  5. Kodama, S, Tokushige S, Sugiyama Y, Sato K, Otsuka J, Shirota Y, Hamada M, Iwata A, Toda T, Tsuji S and Terao Y. Rituximab improves not only back stiffness but also “stiff eyes” in stiff person syndrome: Implications for immune-mediated treatment. J Neurol Sci 408: 116506, 2020. https://doi.org/10.1016/j.jns.2019.116506.
  6. Takiyama Y, Nan H, Ichinose Y, Tanaka M, Koh K, Ishiura H, Mitsui J, Mizukami H, Morimoto M, Hamada S, Ohtsuka T and Tsuji S. UBAP1 mutations cause juvenile onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes. J Hum Genet 64, 1055-1065, 2019. https://doi.org/10.1038/s10038-019-0670-9.
  7. Naruse H, Takahashi Y, Ishiura H, Matsukawa T, Mitsui J, Ichikawa Y, HamadaM, Shimizu J, Goto J, Toda T and Tsuji S. Prominent spasticity and hyperreflexia of the legs in a Nepalese patient with Friedreich ataxia. Intern Med 58:2865-2869, 2019. doi: 10.2169/internalmedicine.2953-19.
  8. Ichikawa Y, Tanaka M, Kurita E, Nakajima M, Oishi C, Goto J, Tsuji S and Chiba A. Novel SLC20A2 mutation in a Japanese patient with idiopathic basal ganglia calcification-1 (IBGC1) associated with dopa-responsive parkinsonism. Human Genome Variation 6: 44, 2019. https://doi.org/10.1038/s41439-019-0073-7.
  9. Nakano Y, Tsunoda K, Yamashita T, Mitsui J, Sato K, Takemoto M, Hishikawa N, Ohta Y, Toda T, Tsuji S and Abe K. Late presented congenital myasthenic syndrome with novel compound heterozygous CHRNE mutations mimicking seronegative myasthenia gravis. Neurol Clin Neurosci 7: 288-290, 2019. https://doi.org/10.1111/ncn3.12317.
  10. Naruse H, Ishiura H, Mitsui J, Takahashi Y, Matsukawa T, Tanaka M, Doi K, Yoshimura J, Morishita S, Goto J, Toda T and Tsuji S. Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS. J Neurol Neurosurg Psychiatry. 90:537-542, 2019. http://dx.doi.org/10.1136/jnnp-2018-318568
  11. Togawa J, Ohi T, Yuan J-H, Takashima H, Furuya H, Takechi S, Fujitake J, Hayashi S, Ishiura H, Naruse H, Mitsui J and Tsuji S. Atypical familial amyotrophic lateral sclerosis with slowly progressing lower extremities-predominant late-onset muscular weakness and atrophy. Intern Med 58:1851-1858, 2019. https://doi.org/10.2169/internalmedicine.2222-18.
  12. Naruse H, Matsukawa T, Ishiura H, Mitsui J, Takahashi Y, Takano H, Goto J, Toda T, and Tsuji S. Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populations. Neurogenet 20: 65-71, 2019. https://doi.org/10.1007/s10048-019-00570-9.
  13. Watanabe T, Anno M, Matsubayashi Y, Nagasako Y, Sakuishi K, Fujimoto Y, Tachibana N, Taniguchi Y, Hayashi T, Oshima Y, Tsuji S and Tanaka S. Hypoglossal Nerve Palsy as a Cause of Severe Dysphagia along with the Oropharyngeal Stenosis due to Occipitocervical Kyphosis. Case Reports in Orthopedics. 2019:7982847, 2019. https://doi.org/10.1155/2019/7982847.
  14. 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. https://doi.org/10.1038/s10038-018-0538-4.
  15. Inuzuka T, Mitsui J, Ishiura H, Iwata A, Fujigasaki H, Tamaki H, Tamaki R, Kito S, Taguchi Y, Tanaka K, Atsuta N, Sobue G, Kondo T, Inoue H, Tsuji S and Hozumi I. Functional evaluation of PDGFB-variants in idiopathic basal ganglia calcification, using patient-derived iPS cells. Sci. Rep. 9:5698, 2019. https://doi.org/10.1038/s41598-019-42115-y.
  16. Hashiguchi S, Doi H, Kunii M, Nakamura Y, Shimuta M, Suzuki E, Koyano S, Okubo M, Kishida H, Shiina M, Ogata K, Hirashima F, Inoue Y, Kubota S, Hayashi N, Nakamura H, Takahashi K, Katsumoto A, Tada M, Tanaka K, Sasaoka T, Miyatake S, Miyake N, Saitsu H, Sato N, Ozaki K, Ohta K, Yokota T, Mizusawa H, Mitsui J, Ishiura H, Yoshimura J, Morishita S, Tsuji S, Takeuchi H, Ishikawa K, Matsumoto N, Ishikawa T and Tanaka F. Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42. Neurobiol Dis. 130:104516, 2019. https://doi.org/10.1016/j.nbd.2019.104516.
  17. Togawa J, Ohi T, Yuan J-H, Takashima H, Furuya H, Takechi S, Fujitake J, Hayashi S, Ishiura H, Naruse H, Mitsui J and Tsuji S. Atypical familial amyotrophic lateral sclerosis with slowly progressing lower extremities-predominant late-onset muscular weakness and atrophy. Int Med. 58: 1851-1858, 2019. https://doi.org/10.2169/internalmedicine.2222-18.
  18. Shirota Y, Ohminami S, Tsutsumi1 R, Terao Y, Ugawa Y, Tsuji S and Hanajima R. Increased facilitation of the primary motor cortex in de novo Parkinson’s disease. Parkinsonism Relat Disord. 66: 125-129, 2019. https://doi.org/10.1016/j.parkreldis.2019.07.022.
  19. 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 and Takiyama Y. Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. Parkinsonism Relat Disord. 61:57-63, 2019. https://doi.org/10.1016/j.parkreldis.2018.11.028.
  20. Koh K, Ichinose Y, Ishiura H, Nan H, Mitsui J, Takahashi J, Sato W, Itoh Y, Hoshino K, Tsuji S, Takiyama Y and Japan Spastic Paraplegia Research Consotium. PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia. J Hum Genet. 64:55-59, 2019. https://doi.org/10.1038/s10038-018-0519-7.
<英文総説>
  1. Stankovic I, Quinn N, Vignatelli L, Antonini A, Berg D, Coon E, Cortelli P, Fanciulli A, Ferreira JJ, Freeman R, Halliday G, Höglinger GU, Iodice V, Kaufmann H, Klockgether T, Kostic V, Krismer F, Lang A, Levin J, Low P, Mathias C, Meissner WG, Kaufmann LN, Palma JA, Panicker JN, Pellecchia MT, Sakakibara R, Schmahmann J, Scholz SW, Singer W, Stamelou M, Tolosa E, Tsuji S, Seppi K, Poewe W, Wenning GK; Movement Disorder Society Multiple System Atrophy Study Group. A critique of the second consensus criteria for multiple system atrophy. 34:975-984, 2019. https://doi.org/10.1002/mds.27701.
<和文総説>
  1. 三井 純.睡眠と疾患:多系統萎縮症.中外医学社,CLINICAL NEUROSCIENCE 2019年7月 (2019; 37(7): 842-845)
  2. 佐々木 秀直、伊藤 瑞規、勝野 雅央、桑原 聡、佐々木 秀直、辻 省次、高橋 祐二、原 一洋、水澤 英洋.わが国の指定難病の診断基準 - 現行基準の課題と展望.中外医学社,CLINICAL NEUROSCIENCE 2019年9月 (2019; 37(9):1113-1116)
  3. 三井 純,近田 彩香,辻 省次.ユビキノールによる治験.中外医学社,CLINICAL NEUROSCIENCE 2019年9月 (2019; 37(9):1135-1137)
  4. 三井 純.MSA-PとMSA-Cは同じ疾患か.アルタ出版,MDSJ letters 2019年11月(2019; 12(2):1-3)
<和文書籍>
  1. 三井 純.「非定型パーキンソニズム ―基礎と臨床―」 II各論 多系統萎縮症 d.治療 2019年5月 文光堂
<国内学会>
  1. 落合 良介,脇田 由貴子,辻野 一,工藤 忍,三井 純,辻 省次.代替マトリックスを用いたヒト脳脊髄液中コエンザイムQ10の分析法の開発及び実試料測定.Japan Bioanalysis Forum 2019.横浜,2019年2月13日.
  2. 近田 彩香,松川敬志,三井純,辻省次,戸田達史,多系統萎縮症の革新的治療法の創出を目指した研究班.多系統萎縮症患者の自然歴調査.第60回日本神経学会学術大会.大阪,2019年5月23日.
  3. Matsukawa T, Yamamoto T, Honda A, Mitsui J, Ishiura H, Hao A, Matsukawa MK, Tanaka M, Miyagawa T, Hamada M, Takahashi Y, Sakuishi K, Iwata A, Shimizu J, Goto J, Kurokawa M, Tsuji S, Toda T. Efficacy of bone marrow transplantation for adolescent/adult-onset cerebral or cerebello-brainstem ALD. 第60回日本神経学会学術大会.大阪,2019年5月22日.
  4. 近田 彩香, 松川 敬志, 三井 純, 尾方 克久, 辻 省次, 戸田 達史.統一多系統萎縮症評価尺度の日本語版の作成と信頼性・妥当性について.第13回パーキンソン病・運動障害疾患コングレス.東京,2019年7月27日.
  5. 三井 純.MSA-PとMSA-Cは同じ疾患か.第13回パーキンソン病・運動障害疾患コングレス.東京,2019年7月27日.
  6. 辻 省次,三井 純.多系統萎縮症に対する医師主導治験.第37回日本神経治療学会.横浜,2019年11月7日.
  7. 和田育江,平野麻理,葛山晴子,何 俊郎,三井 純,辻 省次,森豊隆志.医師主導治験における患者レジストリーからの被験者リクルート.第40回日本臨床薬理学会学術総会.東京,2019年12月5日.
<国際学会>
  1. Tsuji S. Multiple system atrophy -Global harmonization for the natural history and clinical trials- 1st SCA Global Conference. Las Vegas, USA, March 27-29, 2019.
  2. Tsuji S. Genome Science of Neurological Diseases. 5th International Forum for Lysosomal Storage Disorders. Tokyo. July 12, 2019.

2018年

<英文原著>
  1. Amano-Takeshige H, Oyama⁠ G⁠, Kanai⁠ K, Miyagawa T, Mitsui J, Ugawa⁠ Y, Tsuji S and Hattori⁠ A Japanese family with mutation in the proteinase inhibitor 12 L47P gene: A case report. J Neurol Sci. 384, 126–128, 2018. https://doi.org/10.1016/j.jns.2017.11.029.
  2. Morimoto S, Hatsuta H, Motoyama R, Kokubo Y, Ishiura H, Tsuji S, Kuzuhara S and Murayama S. Optineurin pathology in the spinal cord of amyotrophic lateral sclerosis/parkinsonism-dementia complex patients in Kii Peninsula, Japan. Brain Pathol. 28:422-426, 2018. https://doi.org/10.1111/bpa.12558.
  3. Naruse H, Ishiura H, Mitsui J, Date H, Takahashi Y, Matsukawa T, Tanaka M, Ishii A, Tamaoka A, Hokkoku K, Sonoo M, Segawa M, Ugawa Y, Doi K, Yoshimura J, Morishita S, Goto J and Tsuji S. Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation. Neurobiol Aging. 61:255.e9-255.e16, 2018. https://doi.org/10.1016/j.neurobiolaging.2017.08.030
  4. Horikawa Y, Hosomichi K, Enya M, Ishiura H, Suzuki Y, Tsuji S, Sugano S, Inoue I, Takeda J. No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODY. J Hum Genet. 63:821-829, 2008. https://doi.org/10.1038/s10038-018-0449-4.
  5. Nagase,M, Yamamoto Y, Mitsui J and Tsuji S. Simultaneous detection of reduced and oxidized forms of coenzyme Q10 in human cerebral spinal fluid as a potential marker of oxidative stress. J Clin Biochem Nutr. 63:205-210, 2018. https://doi.org/10.3164/jcbn.17-131.
  6. Mitsutake A, Matsukawa T, Ishiura H, Mitsui J, Taira K, Tokushige S, Iwata A, Terao Y, Shimizu J, Sakai N, Tsuji S. A case of late-onset Krabbe disease which showed subacute progression of spastic paresis with bilateral spinal cord lesions. Neurol. Clin. Neurosci. 6:104-106, 2018. https://doi.org/10.1111/ncn3.12188.
  7. Tanabe H, Higuchi Y, Yuan J-H , Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, Sunami Y, Kono Y, Ishigaki Y, Yanamoto S, Fukae J, Kida H, Morita M, Tsuji S and Takashima H. Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan. J Peripheral Nervous System. 23:40-48, 2018. https://doi.org/10.1111/jns.12252.
  8. Misawa S, Kuwabara S, Sato Y, Yamaguchi N, Nagashima K, Katayama K, Sekiguchi Y,  Iwai Y, Amino H, Suichi T, Yokota T, Nishida Y, Kanouchi T, Kohara N, Kawamoto M, Ishii J, Kuwahara M, Suzuki H, Hirata K, Kokubun N, Masuda R, Kaneko J, Yabe I, Sasaki H, Kaida K, Takazaki H, Suzuki N, Suzuki S, Nodera H, Matsui N, Tsuji S, Koike H, Yamasaki R, Kusunoki S, for the Japanese Eculizumab Trial for GBS (JET-GBS) Study Group. Safety and efficacy of eculizumab in Guillain-Barré syndrome: a multicentre, double-blind, randomised phase 2 trial. Lancet Neurol. 17:519-529, 2018. https://doi.org/10.1016/S1474-4422(18)30114-5.
  9. Yamaguchi N, Mano T, Ohtomo R, Ishiura H, Almansour A, Mori H, Kanda J, Shirota Y, Taira K, Morikawa T, Ikemura M, Yanagi Y, Murayama S, Shimizu J, Sakurai Y, Tsuji S, and Iwata1 A. An Autopsy Case of Familial Neuronal Intranuclear Inclusion Disease with Dementia and Neuropathy. Int Med. 57:3459-3462, 2018. https://doi.org/10.2169/internalmedicine.1141-18.
  10. Horita S, Simsek E, Simsek T, Ishiura H, Nakamura M, Satoh N, Suzuki A, Tsukada H, Tsuji S and Nangaku M. SLC4A4 compound heterozygous mutations in exon-intron boundary regions cause severe proximal renal tubular acidosis with extrarenal symptoms: a case report. BMC Medical Genetics. 19:103, 2018. https://doi.org/10.1186/s12881-018-0612-y.
  11. Koh K, Ishiura H, Beppu M, Shimazaki H, Ichinose Y, Mitsui J, Kuwabara S, Tsuji S, Takiyama Y, Japan Spastic Paraplegia Research Consortium. Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment. J Hum Genet. 63:1009-1013, 2018. https://doi.org/10.1038/s10038-018-0477-0.
  12. Tokushige S, Terao Y, Matsuda S, Furubayashi T, Sasaki T, Inomata-Terada S, Yugeta A, Hamada M, Tsuji S and Ugawa Y. Does the Clock Tick Slower or Faster in Parkinson’s Disease? – Insights Gained From the Synchronized Tapping Task. Frontiers in Psychology. 11 July 2018 https://doi.org/10.3389/fpsyg.2018.01178.
  13. Koh K, Ishiura H, Tsuji S and Takiyama Y. JASPAC: Japan Spastic Paraplegia Research Consortium. Brain Sci. 8:153, 2018. https://doi.org/10.3390/brainsci8080153.
  14. Ishiura H, Doi K, Mitsui J, Yoshimura 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, Koike 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 S and Tsuji S. Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy. Nat Genet. 50:581-590, 2018. https://doi.org/10.1038/s41588-018-0067-2.
  15. Tokushige S, Matsuda S, Oyama G, Shimo Y, Umemura A, Sasaki T, Inomata-Terada S, Yugeta A, Hamada M, Ugawa Y, Tsuji S, Hattori N and Terao Y. Effect of subthalamic nucleus deep brain stimulation on visual scanning. Clinical Neurophysiology. 129:2421-2432, 2018. https://doi.org/10.1016/j.clinph.2018.08.003.
  16. Kurihara M, Bannai T, Otsuka J, Kawabe Matsukawa M, Terao Y, Shimizu J and Tsuji S. Optic neuropathy and decorticate-like posture as presenting symptoms of Bickerstaff’s brainstem encephalitis: A case report and literature review. Clin Neurol Neurosurg. 173:159-162, 2018. https://doi.org/10.1016/j.clineuro.2018.08.019.
  17. Kodama S, Mano T, Kakumoto T, Ishiura H, Hagiwara A, Kamiya K, Hayashi T and Tsuji S. Ketotic hyperglycemia-related seizure with reversible white matter lesion: Metabolic implication of its reversibility based on magnetic resonance spectroscopy study. J Neurol Sci. 390:20-21, 2018. https://doi.org/10.1016/j.jns.2018.04.006.
  18. Yoshikawa K, Kuwahara M, Saigoh K, Ishiura H, Yamagishi Y, Hamano Y, Samukawa M, Suzuki H, Hirano Mitsui J, Tsuji S and Kusunoki S. The novel de novo mutation of KIF1A causes spastic paraplegia 30. eNeurologicalSci 14:34-37, 2018. https://doi.org/10.1016/j.ensci.2018.11.026.
  19. Nishioka Y, Shindoh J, Inagaki Y, Gonoi W, Mitsui J, Abe H, Yoshioka R, Yoshida S, Fukayama M, Tsuji S, Hashimoto M, Hasegawa K and Kokudo N. Host MICA Polymorphism as a Potential Predictive Marker in Response to Chemotherapy for Colorectal Liver Metastases. Dig Dis. 36:437-445, 2018. https://doi.org/10.1159/000490411.
  20. Nakamoto FK, Okamoto S, Mitsui J, Sone T, Ishikawa M, Yamamoto Y, Kanegae Y, Nakatake Y, Imaizumi K, Ishiura H, Tsuji S and Okano H. The pathogenesis linked to coenzyme Q10 insufficiency in iPSC-derived neurons from patients with mul-tiple-system atrophy. Sci Rep. 28:14215, 2018. https://doi.org/10.1038/s41598-018-32573-1.
  21. Cen Z, Jiang Z, Chen Y, Zheng X, Xie F, Yang X, Lu X, Ouyang Z, Wu H, Chen S, Yin H, Qiu X, Wang S, Ding M, Tang Y, Yu F, Li C, Wang T, Ishiura H, Tsuji S, Jiao C, Liu C, Xiao J and Luo W. Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1. Brain. 141:2280-2288, 2018. https://doi.org/10.1093/brain/awy160.
  22. Kurihara M, Sasaki T, Ishiura H and Tsuji S. HIV Dementia with a Decreased Cardiac 123I-metaiodobenzylguanidine Uptake Masquerading as Dementia with Lewy Bodies. Intern Med. 57:3007-3010, 2018. https://doi.org/10.2169/internalmedicine.0876-18.
  23. Sekine S, Kaneko M, Tanaka M, Ninomiya Y, Kurita H, Inden M, Yamada M, Hayashi Y, Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, Toda T, Yamashita S, Yamada K, Koide T, Yaguchi H, Mitsui J, Ishiura H, Yoshimura J, Doi K, Morishita S, Sato K, Nakagawa M, Yamaguchi M, Tsuji S and Takashima H. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy. Brain. 141:1622-1636, 2018. https://doi.org/10.1093/brain/awy104.
<英文総説>
  1. Walsh RR, Krismer F, Galpern WR, Wenning GK, Low PA, Halliday G, Koroshetz WJ, Holton J, Quinn NP, Rascol O, Shaw LM, Eidelberg D, Bower P, Cummings JL, Abler V, Biedenharn J, Bitan G, Brooks DJ, Brundin P, Fernandez H, Fortier P, Freeman R, Gasser T, Hewitt A, Höglinger GU, Huentelman MJ, Jensen PH, Jeromin A, Kang UJ, Kaufmann H, Kellerman L, Khurana V, Klockgether T, Kim WS, Langer C, LeWitt P, Masliah E, Meissner W, Melki R, Ostrowitzki S, Piantadosi S, Poewe W, Robertson D, Roemer C, Schenk D, Schlossmacher M, Schmahmann JD, Seppi K, Shih L, Siderowf A, Stebbins GT, Stefanova N, Tsuji S, Sutton S, Zhang J. Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting. Neurology. 90:74-82, 2018. https://doi.org/10.1212/WNL.0000000000004798.
<国際学会>
  1. Shoji Tsuji. Hematopoietic stem cell transplantation for adult cerebral form of adrenoleukodystrophy. The 5th IMSUT-CGCT Symposium. Tokyo, Jan 30, 2018.
  2. Tsuji S. Comprehensive genome sequencing to elucidate the molecular basis of MSA. 6th International Multiple System Atrophy Congress. NYC, U.S.A., March 1st, 2018.
  3. Tsuji S. Identification of COQ2 gene as a susceptibility gene for multiple system atrophy (MSA), a rare neurodegenerative diseases, and supplementation with a high dose ubiquinol as a phase 2 clinical trial for MSA. The 9th International Symposium of the Society for Research on the Cerebellum and Ataxias. Taipei, May 16-19, 2018.
  4. Tsuji S. Searching for MSA genes. Multiple System Atrophy Study Group (MoDiMSA) Annual Meeting. Hong Kong. Oct 6, 2018.
  5. Tsuji S. Neurogenomics initiatives between Japan and Russia to accelerate elucidation of molecular basis of neurological diseases. Russian Science Foundation – Japan Agency for Medical Research and Development. Moscow. Sep 17, 2018.
<国内学会>
  1. 松川 敬志, 三井 純, 石浦 浩之, 山本 知孝, 羽尾 暁人, 松川 美穂, 田中 真生, 張 香理, 宮川 統爾, 濱田 雅, 高橋 祐二, 林 俊宏, 岩田 淳, 清水 潤, 後藤 順, 戸田 達史, 辻 省次.HSCT for adult-onset ALD: Background factors leading to early diagnosis of the brain involvement. 第59回日本神経学会学術大会.札幌,2018年5月23日.
  2. 近田 彩香,松川 敬志,三井 純,尾方 克久,戸田 達史,辻 省次.日本語版統一多系統萎縮症評価尺度の信頼性・妥当性について.第59回日本神経学会学術大会.札幌,2018年5月24日.
  3. 織茂 賢太,栗原 正典,近田 彩香,三井 純,戸田 達史.多系統萎縮症におけるMIBG心筋シンチと臨床像に関する検討.第59回日本神経学会学術大会.札幌,2018年5月24日.
  4. 辻 省次.ゲノムから孤発性神経疾患の解明へ -オーバービュー- 第59回日本神経学会学術大会.札幌,2018年5月25日.
  5. 三井 純.ゲノムから孤発性神経疾患が解明できるか? 第59回日本神経学会学術大会.札幌,2018年5月25日.

2017年

<英文原著>
  1. Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige S, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y and Tsuji S. Three-year follow-up of high-dose ubiquinol supplementation in a case of familial multiple system atrophy with compound heterozygous COQ2 mutations. Cerebellum. 16:664-672, 2017.
<英文短信>
  1. Tsuji S, Mitsui J. Letter re: A genome-wide association study in multiple system atrophy. Neurology. 88:1296, 2017.
<和文総説>
  1. 三井 純.立ちくらみ(多系統萎縮症).南江堂,内科 2017年4月(2017; 119(4): 591-4)
  2. 三井 純.脊髄小脳変性症のゲノム医療.科学評論社,神経内科 2017年6月 (2017; 86(6):667-671)
  3. 三井 純.多系統萎縮症の新しい遺伝子.科学評論社,神経内科 2017年8月 (2017; 87(2):)
<和文書籍>
  1. 三井 純,辻 省次.「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」第II章-B-10.多系統萎縮症. 2017年9月 南江堂
  2. 三井 純.「運動失調のみかた、考えかた ―小脳と脊髄小脳変性症―」第Ⅳ章4.MSAの治療戦略. 2017年9月 中外医学社
<国際学会>
  1. Jun Mitsui, Ken Koguchi, Toshimitsu Momose, Miwako Takahashi, Takashi Matsukawa, Tsutomu Yasuda, Shin-ichi Tokushige, Hiroyuki Ishiura, Jun Goto, Shigeaki Nakazaki, Tomoyoshi Kondo, Hidefumi Ito, Yorihiro Yamamoto, and Shoji Tsuji. Three-year follow-up of high-dose ubiquinol supplementation in a case of familial multiple system atrophy with compound heterozygous COQ2 mutations (poster). 21st International Congress of Parkinson’s Disease and Movement Disorders. Vancouver Convention Centre. Vancouver, Canada, Jun 6th, 2017
<国内学会>
  1. 三井 純.ゲノム情報と臨床情報の統合的解析(口頭発表).東京大学ゲノム医科学研究機構第2回 シンポジウム,東京,2017年3月25日.
  2. 三井 純.多系統萎縮症の遺伝学的検討(口頭発表).若手神経内科医によるNeurology & Clinical Neuroscience Lecture in KOBE,神戸,2017年3月24日.

2016年

<英文原著>
  1. Mitsui J, Matsukawa T, Yasuda T, Ishiura H, Tsuji S. Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy. JAMA Neurol. 73:977-980, 2016.
  2. Paap B, Roeske S, Durr A, Schöls L, Ashizawa T, Boesch S, Delatycki MB, Giunti P, . Lehericy S, Mariotti C, Melegh B, Pandolfo M, Tallaksen C, Timmann D, Tsuji S, Schulz J, van de Warrenburg BP, Klockgether T. Standardized assessment of hereditary ataxia patients in clinical studies. Movement Disorders Clinical Practice. 2016 Feb 11;3:230–240.
<英文短信>
  1. Mitsui J, Tsuji S. Plasma Coenzyme Q10 Levels and Multiple System Atrophy-Reply. JAMA Neurol. 73:1499-1500, 2016.
<和文総説>
  1. 三井 純.多系統萎縮症.「遺伝子医学MOOK 別冊 シリーズ:最新遺伝医学研究と遺伝子カウンセリング シリーズ2:「最新精神・神経遺伝医学研究と遺伝子カウンセリング」」 2016年1月 メディカルドゥ社
  2. 三井 純,辻 省次. 多系統萎縮症 ‒‒患者レジストリーと治験.科学評論社,神経内科 2016年12月 (2016; 85(6): 652-6)
  3. 三井 純. 多系統萎縮症発症における遺伝因子 科学評論社,神経内科 2016年5月 (2016; 84(5): 458-463)
<国内学会>
  1. 三井 純.遺伝子研究におけるメタ解析(口頭発表).第57回神経学会学術大会,生涯教育講演,神戸,2016年5月19日.

2015年

<英文原著>
  1. Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM-Y, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, and Tsuji S. Variants associated with Gaucher disease in multiple system atrophy. Ann Clin Transl Neurol. 2:417-26, 2015.
  2. Saigoh K, Mitsui J, Hirano M, Shioyama M, Samukawa M, Ichikawa Y, Goto J, Tsuji S, Kusunoki S. The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene. Parkinsonism Relat Disord. 21:332-334, 2015.
<和文書籍>
  1. 三井 純.「Annual Review神経内科2015」多系統萎縮症の遺伝学.中外医学社, p. 35-41
<和文総説>
  1. 三井 純.多系統萎縮症.医歯薬出版株式会社,医学のあゆみ 2015年12月(2015; 255(10): 1047-1051)
<国際学会>
  1. Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, JAMSAC, NAMSA-SG, Tsuji S. Variants associated with Gaucher disease in multiple system atrophy (oral presentation). The 67th American Academy of Neurology Annual Meeting, Washington DC, April 22nd 2015
<国内学会>
  1. 三井 純,松川 敬志,佐々木 秀直,矢部一郎,松島 理明,Alexandra Dürr,Alexis Brice,高嶋 博,JAMSAC,NAMSA-SG,辻 省次.多系統萎縮症の遺伝学的検討(口頭発表).第56回神経学会学術大会,シンポジウム,新潟,2015年5月21日.

2014年

<英文原著>
  1. Mitsui J, Tsuji S. Mutant COQ2 in multiple-system atrophy. N Engl J Med. 371:82-83, 2014.
<英文総説>
  1. Mitsui J, Tsuji S. Genomic aspects of sporadic neurodegenerative diseases. Biochem Biophys Res Commun. 452:221-225, 2014.
<和文書籍>
  1. 三井 純.「神経内科研修ノート」多系統萎縮症. 2014年 p. 314-7 診断と治療社
  2. 三井 純.「別冊日本臨床 新領域別症候群シリーズNo.27 神経症候群(第2版)」多系統萎縮症. p.341-344 2014年3月 日本臨床社
<和文総説>
  1. Tsuji S. Susceptibility gene in multiple system atrophy (MSA). Rinsho Shinkeigaku. 54:969-971, 2014.
  2. 三井 純.多系統萎縮症の関連遺伝子.北隆館,BIO Clinica 2014年4月 (2014; 29(6): 93-7)
<国際学会>
  1. Mitsui J. Genetics in Multiple System Atrophy (oral presentation). The 13th International Parkinson’s disease Symposium in Takamatsu. Takamatsu, February 21st-22nd, 2014
  2. Mitsui J. Mutations in COQ2 in Familial and Sporadic Multiple-system Atrophy (oral presentation). 3rd GCOE Workshop between BGI and UT. Tokyo, March 20th, 2014
<国内学会>
  1. 三井 純,松川 敬志,石浦 浩之,市川 弥生子,後藤 順,JAMSAC,村山 繁雄,高嶋 博,佐々木 秀直,辻 省次.多系統萎縮症の疾患関連遺伝子の探索(口頭発表).第55回神経学会学術大会,博多,2014年5月23日.

2013年

<英文原著>
  1. Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Iwata A, Goto J, Yamamoto Y, Komata M, Shirahige K, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Takashima H, Kuwano R, Watanabe H, Ito M, Sobue G, Soma H, Yabe I, Sasaki H, Aoki M, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Dürr A, Brice A, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Shults CW, Tanner CM, Kukull WA, Lee V M-Y, Masliah E, Low PA, Sandroni P, Trojanowski JQ, Ozelius L, Foroud T and Tsuji S. Mutations of COQ2 in familial and sporadic multiple system atrophy. N Engl J Med. 369:233-244, 2013.
<和文総説>
  1. 三井 純.パーキンソン病と多系統萎縮症における遺伝因子.医歯薬出版株式会社,医学のあゆみ 2013年11月(Vol. 247, No.5, 445-449)
  2. 三井 純.パーソナルゲノミックスに基づく孤発性神経変性疾患の解明.羊土社,実験医学 2013年7月増刊号(2013; 31(15): 160-164)
<国際学会>
  1. Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Goto J, Yamamoto Y, Shirahige K, Takahashi H, Onodera O, Nishizawa M, Kondo T, Murayama S, Japan Multiple System Atrophy Consortium, Japanese Genetic Study Consortium for Alzheimer Disease, Japanese Parkinson Disease Susceptibility Gene Consortium, Japanese Consortium for Amyotrophic Lateral Sclerosis research, Dürr A, Brice A, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S for NAMSA-SG, and Tsuj S. Mutations of COQ2 in Familial and Sporadic Multiple System Atrophy (poster). The 63rd American Society of Human Genetics Annual Meeting, Boston, October 24th 2013
  2. JAMSAC (Japan Multiple System Atrophy Research Consortium), Jun Mitsui, Yaeko Ichikawa, Jun Goto, Shoji Tsuji. Molecular genetics of multiple system atrophy: results from the Japan Multiple System Atrophy Research Consortium (poster). The 17th International Congress of Parkinson’s disease and Movement Disorder, Sydney, June 16-20 2013.
<国内学会>
  1. 三井 純.多系統萎縮症の遺伝子解析(口頭発表).千代田学術講演会,東京,2013年11月13日
  2. 三井 純,松川 敬志,石浦 浩之,福田 陽子,市川 弥生子,伊達 英俊,Budrul Ahsan,中原 康雄,百瀬 義雄,高橋 祐二,岩田 淳,後藤 順,The MSA Research Collaboration,辻 省次.COQ2変異は家族性・孤発性多系統萎縮症と関連する(口頭発表).第58回日本人類遺伝学会,仙台,2013年11月22日.

2012年

<国内学会>
  1. 三井 純,石浦 浩之,市川 弥生子,後藤 順,辻 省次.家族性MSAおよびMSA・PD多発家系の全ゲノム解析(ポスター).第53回神経学会総会,東京,2012年5月25日.

2011年

<和文総説>
  1. Ichikawa Y, Goto J, Nakahara Y, Mitsui J, Tsuji S. Therapeutic trial design issues for future disease-modifying therapy of multiple system atrophy. Rinsho Shinkeigaku. 51:910-913, 2011.

2008年

<英文原著>
  1. Tsuji S, Onodera O, Goto J, Nishizawa M; Study Group on Ataxic Diseases. Sporadic ataxias in Japan–a population-based epidemiological study. Cerebellum. 7:189-197, 2008.

2007年

<英文原著>
  1. Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, Kakita A, Yamada M, Takahashi H, Hirasawa M, Mizuno Y, Ogata K, Goto J, Kanazawa I, Nishizawa M, Tsuji S. Multiplex families with multiple system atrophy. Arch Neurol. 64:545-51, 2007.

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