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バイオリソースを活用した論文一覧

NCNPの2019年の発表、掲載論文に関する検索結果

Search results

Item: 5

No. Publication
  1. Emery‐Dreifuss muscular dystrophy‐related myopathy with TMEM43 mutations
    Author(s):
      Mukai T, Mori-Yoshimura M, Nishikawa A, Hokkoku K, Sonoo M, Nishino I, Takahashi Y.
    Source:
      MUSCLE & NERVE 59:E5-E7, 2019
    PMID:
      30311943
  2. Author(s):
      Ozawa K, Mochizuki K, manabe Y, Yoshikura N, Shimohata T, Nishino I, Goto Y.
    Source:
      DOCUMENTA OPHTHALMOLOGICA 138:147-152, 2019
    PMID:
      30701423
  3. Author(s):
      Gotoh L, Yamada M, Hattori K, Sasayama D, Noda T, Yoshida S, Kunugi H, Yamada M.
    Source:
      PSYCHIATRY RESEARCH 273:331-335, 2019
    PMID:
      30682553
  4. Author(s):
      Itagaki K, Takebayashi M, Abe H, Shibasaki C, Kajitani N, Okada-Tsuchioka M, Hattori K, Yoshida S, Kunugi H, et al.
    Source:
      INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY 22:261-269, 2019
    PMID:
      30715387
  5. A polymorphism of the methylenetetrahydrofolate reductase gene confers susceptibility to schizophrenia and related brain changes
    Author(s):
      Ota M, Sato N, Yoshida F, Hattori K, Hidese S, Teraishi T, Kunugi H.
    Source:
      SCHIZOPHRENIA RESEARCH, 2019
    PMID:
      30852115

NCNPの2018年の発表、掲載論文に関する検索結果

Search results

Item: 39

No. Publication
  1. Author(s):
      Kameyama T, Ohuchi K, Funato M, Ando S, Inagaki S, Sato A, Seki J, Kawase C, Tsuruma K, et al.
    Source:
      FRONTIERS IN PHARMACOLOGY 9:1402, 2018
    PMID:
      30559667
  2. Author(s):
      Sasaki-Honda M, Jonouchi T, Arai M, Hotta A, Mitsuhashi S, Nishino I, Matsuda R, Sakurai H.
    Source:
      HUMAN MOLECULAR GENETICS 27:4024-4035, 2018
    PMID:
      30107443
  3. Three novel recessive DYSF mutations identified in three patients with muscular dystrophy, limb-girdle, type 2B
    Author(s):
      Okubo M, Iida A, Hayashi S, Mori-Yoshimura M, Oya Y, Watanabe A, Arahata H, El Sherif R, Noguchi S, et al.
    Source:
      JOURNAL OF THE NEUROLOGICAL SCIENCES 395:169-171, 2018
    PMID:
      30366248
  4. Author(s):
      Ohta Y, Tadokoro K, Sasaki R, Takahashi Y, Sato K, Takemoto M, Hishikawa N, Shang J, Yamashita T, et al.
    Source:
      JOURNAL OF CLINICAL NEUROSCIENCE 58:215-217, 2018
    PMID:
      30327220
  5. Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation
    Author(s):
      Tadokoro K, Ohta Y, Sasaki R, Takahashi Y, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, et al.
    Source:
      JOURNAL OF THE NEUROLOGICAL SCIENCES 393:142-144, 2018
    PMID:
      30195123
  6. Author(s):
      Oitani Y, Ishiyama A, Kosuga M, Iwasawa K, Ogata A, Tanaka F, Takeshita E, Shimizu-Motohashi Y, Komaki H, et al.
    Source:
      BRAIN AND DEVELOPMENT 40:837-840, 2018
    PMID:
      29778277
  7. Author(s):
      Leoyklang P, Class B, Noguchi S, Gahl WA, Carrillo N, Nishino I, Huizing M, Malicdan MC.
    Source:
      MUSCLE & NERVE 58:286-292, 2018
    PMID:
      29603301
  8. Author(s):
      Kumutpongpanich T, Owattanapanich W, Tanboon J, Nishino I, Boonyapisit K.
    Source:
      NEUROMUSCULAR DISORDERS 28:610-613, 2018
    PMID:
      29910095
  9. Author(s):
      Ishiyama A, Iida A, Hayashi S, Komaki H, Sasaki M, Nonaka I, Noguchi S, Nishino I.
    Source:
      HUMAN GENOME VARIATION 5:19, 2018
    PMID:
      30083363
  10. A new familial distal myopathy in Japan with predominant upper extremities
    Author(s):
      Takahashi Y, Ohta Y, Sasaki R, Tadokoro K, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, et al.
    Source:
      JOURNAL OF THE NEUROLOGICAL SCIENCES 390:205-207, 2018
    PMID:
      29801888
  11. Anti-mitochondrial antibody-associated myositis with eosinophilia and dropped head
    Author(s):
      Shimizu H, Nishino I, Ueda T, Kohara N, Nishioka H.
    Source:
      ENEUROLOGICALSCI 11:15-16, 2018
    PMID:
      29928712
  12. Author(s):
      Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, et al.
    Source:
      HUMAN GENOME VARIATION 5:9, 2018
    PMID:
      29899994
  13. Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
    Author(s):
      Ishiyama A, Kimura Y, Iida A, Saito Y, Miyamoto Y, Okada M, Sato N, Nishino I, Sasaki M.
    Source:
      NEUROLOGY 90:974-976, 2018
    PMID:
      29695595
  14. Author(s):
      Ishiyama A, Muramatsu K, Uchino S, Sakai C, Matsushima Y, Makioka N, Ogata T, Suzuki E, Komaki H, et al.
    Source:
      CLINICAL GENETICS 93:1103-1106, 2018
    PMID:
      29344937
  15. A mild myopathy with anti-SRP plus anti-PL-12 antibodies successfully treated by oral steroid monotherapy
    Author(s):
      Tadokoro K, Ohta Y, Sasaki R, Takahashi Y, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, et al.
    Source:
      JOURNAL OF THE NEUROLOGICAL SCIENCES 388:7-9, 2018
    PMID:
      29627033
  16. Author(s):
      Kondo T, Yasuda T, Mukaida K, Otsuki S, Kanzaki R, Miyoshi H, Hamada H, Nishino I, Kawamoto M.
    Source:
      JOURNAL OF ANESTHESIA 32:174-181, 2018
    PMID:
      29344738
  17. Author(s):
      Kageyama Y, Kasahara T, Kato M, Sakai S, Deguchi Y, Tani M, Kurida K, Hattori K, Yoshida S, et al.
    Source:
      JOURNAL OF AFFECTIVE DISORDERS 233:15-20, 2018
    PMID:
      28633757
  18. Author(s):
      Lin H, Miyauchi K, Harada T, Okita R, Takeshita E, Komaki H, Fujioka K, Yagasaki H, Goto Y, et al.
    Source:
      NATURE COMMUNICATIONS 9:1875, 2018
    PMID:
      29760464
  19. Author(s):
      Kushima I, Aleksic B, Nakatochi M, Shimamura T, Okada T, Uno Y, Morikawa M, Ishizuka K, Shiino T, et al.
    Source:
      CELL REPORTS 24:2838-2856, 2018
    PMID:
      30208311
  20. Author(s):
      Iida A, Takeshita E, Kosugi S, Kamatani Y, Momozawa Y, Kubo M, Nakagawa E, Kurosawa K, Inoue K, et al.
    Source:
      HUMAN GENOME VARIATION 6:1, 2018
    PMID:
      30534410
  21. Author(s):
      Teraishi T, Kajiwara M, Hori H, Sasayama D, Hidese S, Matsuo J, Ishida I, Kajiwara Y, Ozeki Y, et al.
    Source:
      JOURNAL OF PSYCHIATRIC RESEARCH 99:142-150, 2018
    PMID:
      29454221
  22. Author(s):
      Yoon HS, Hattori K, Sasayama D, Kunugi H.
    Source:
      JOURNAL OF AFFECTIVE DISORDERS 232:134-138, 2018
    PMID:
      29486339
  23. Author(s):
      Ikeda M, Takahashi A, Kamatani Y, Momozawa Y, Saito T, Kondo K, Shimasaki A, Kawase K, Sakusabe T, et al.
    Source:
      SCHIZOPHRENIA BULLETIN, 2018
    PMID:
      30285260
  24. Author(s):
      Cortese A, Laura M, Casali C, Nishino I, Hayashi YK, Magri S, Taroni F, Stuani C, Saveri P, et al.
    Source:
      EUROPEAN JOURNAL OF NEUROLOGY 25:154-163, 2018
    PMID:
      29029362
  25. Author(s):
      Ishii T, Hattori K, Miyakawa T, Watanabe K, Hidese S, Sasayama D, Ota M, Teraishi T, Hori H, et al.
    Source:
      Biochem Biophys Res Commun. 497:683-8, 2018
    PMID:
      29454970
  26. Author(s):
      Ishiwata S, Hattori K, Sasayama D, Teraishi T, Miyakawa T, Yokota Y, Matsumura R, Nishikawa T, Kunugi H.
    Source:
      J Affect Disord. 226:155-62, 2018
    PMID:
      28985587
  27. Author(s):
      Itoh M, Ide S, Iwasaki Y, Saito T, Narita K, Dai H, Yamakura S, Furue T, Kitayama H, et al.
    Source:
      Brain Dev 40:259-267, 2018
    PMID:
      29217415
  28. Author(s):
      Kageyama Y, Kasahara T, Kato M, Sakai S, Deguchi Y, Tani M, Kuroda K, Hattori K, Yoshida S, et al.
    Source:
      J Affect Disord. 233:15-20, 2018
    PMID:
      28633757
  29. Author(s):
      Kubota A, Ishiura H, Mitsui J. Sakuishi K Iwata A, Yamamoto T, Nishino I, Tsuji S, Shimizu J,
    Source:
      INTERNAL MEDICINE 57:877-882, 2018
    PMID:
      29225264
  30. Author(s):
      Matsubara S, Bokuda K, Asano Y, Morishima R, Sugaya K, Miyamoto K, Koide R, Komori T, Suzuki S, et al.
    Source:
      NEUROMUSCULAR DISORDERS 28:283-288, 2018
    PMID:
      29402601
  31. Author(s):
      Nagata Y, Hirayama A, Ikeda S, Shirahata A, Shoji F, Maruyama M, Kayano M, Bundo M, Hattori K, et al.
    Source:
      Biomark Res. 6:5, 2018
    PMID:
      29387418
  32. Author(s):
      Ohsawa Y, Hagiwara H, Nishimatsu S, Hirakawa A, Kamimura N, Ohtsubo H, Fukai Y, Murakami T, Koga Y, et al.
    Source:
      J Neurol Neurosurgery Psychiatr (in press)
    PMID:
      29666206
  33. Author(s):
      Pogoryelova O, Cammish P, Mansbach H, Argov Z, Nishino I, Skrinar A, Chan Y, Nafissi S, Shamshiri H, et al.
    Source:
      NEUROMUSCULAR DISORDERS 28:158-168, 2018
    PMID:
      29305133
  34. New Criteria Needed for Antisynthetase Syndrome-Reply
    Author(s):
      Suzuki S, Uruha A, Nishino I.
    Source:
      JAMA Neurol 75:259-260, 2018
    PMID:
      29255891
  35. A 62-Year-Old Woman with A History of Muscle Pain and Skin Rash for 1 Month
    Author(s):
      Tanboon J, Uruha A, Hamanaka K, Hasegawa J, Nishino I.
    Source:
      Brain Pathol 28:121-122, 2018
    PMID:
      29265633
  36. Author(s):
      Teraishi T, Kajiwara M, Hori H, Sasayama D, Hidese S, Matsuo J, Ishida I, Kajiwara Y, Ozeki Y, et al.
    Source:
      J Psychiatr Res. 99:142-50, 2018
    PMID:
      29454221
  37. A 31-Year-Old Man with Slowly Progressive Limb Muscle Weakness and Respiratory Insufficiency
    Author(s):
      Uruha A, Hayashi YK, Mori-Yoshimura M, Oya Y, Kanai M, Murata M, Nishino I.
    Source:
      Brain Pathol 28:123-124, 2018
    PMID:
      29265629
  38. Author(s):
      Yoon HS, Hattori K, Sasayama D, Kunugi H.
    Source:
      J Affect Disord. 232:134-8, 2018
    PMID:
      29486339
  39. Author(s):
      Zhu W, Eto M, Mitsuhashi S, Takata K, Beck G, Sumi-Akamaru H, Mochizuki H, Sakoda S, Takahashi MP, et al.
    Source:
      NEUROMUSCULAR DISORDERS 28:154-157, 2018
    PMID:
      29307446

NCNPの2017年の発表、掲載論文に関する検索結果

Search results

Item: 41

No. Publication
  1. Author(s):
      Araki W, Hattori K, Kanemaru K, Yokoi Y, Omachi Y, Takano H, Sakata M, Yoshida S, Tsukamoto T, et al.
    Source:
      Biomark Res. 5:28, 2017
    PMID:
      29018524
  2. Author(s):
      Cho A, Malicdan MCV, Miyakawa M, Nonaka I, Nishino I, Noguchi S.
    Source:
      HUMAN MOLECULAR GENETICS 26:3081-3093, 2017
    PMID:
      28505249
  3. Author(s):
      Hanai S, Sukigara S, Dai H, Owa T, Horike S, Otsuki T, Saito T, Nakagawa E, Ikegaya N, et al.
    Source:
      Am J Pathol. (in press)
    PMID:
      28427592
  4. Author(s):
      Hatakeyama H, Goto Y.
    Source:
      Am J Pathol. 187(1):110-121. 2017.
    PMID:
      27855277
  5. Author(s):
      Hibino S, Takeda A, Nishino I, Iwata N, Nakano M, Tanaka K, Yamakawa S, Nagai T, Uemura O.
    Source:
      INTERNAL MEDICINE 56:1849-1853, 2017
    PMID:
      28717081
  6. Author(s):
      Hidese S, Hattori K, Sasayama D, Miyakawa T, Matsumura R, Yokota Y, Ishida I, Matsuo J, Noda T, et al.
    Source:
      Prog Neuropsychopharmacol Biol Psychiatry. 76:12-18. 2017.
    PMID:
      28238731
  7. Author(s):
      Hori I, Otomo T, Nakashima M, Miya F, Negishi Y, Shiraishi H, Nonoda Y, Magara S, Tohyama J, et al.
    Source:
      SCIENTIFIC REPORTS 7:3552-3552, 2017
    PMID:
      28615637
  8. Author(s):
      Ikeda T, Nakahara A, Nagano R, Utoyama M, Obara M, Moritake H, Uechi T, Mitsui J, Ishiura H, et al.
    Source:
      JOURNAL OF HUMAN GENETICS 62:473-480, 2017
    PMID:
      27928163
  9. Author(s):
      Inui T, Anzai M, Takezawa Y, Endo W, Kakisaka Y, Kikuchi A, Onuma A, Kure S, Nishino I, et al.
    Source:
      JOURNAL OF HUMAN GENETICS 62:653-655, 2017
    PMID:
      28148925
  10. Author(s):
      Ishiwata S, Hattori K, Sasayama D, Teraishi T, Miyakawa T, Yokota Y, Matsumura R, Yoshida F, Nishikawa T, et al.
    Source:
      Psychiatry Res. 254:244-50, 2017
    PMID:
      28477547
  11. Author(s):
      Ishiyama A, Sakai C, Matsushima Y, Noguchi S, Mitsuhashi S, Endo Y, Hayashi YK, Saito Y, Nakagawa E, et al.
    Source:
      NEUROLOGY: GENETICS 3:e184-e184, 2017
    PMID:
      28913435
  12. Author(s):
      Kadoya M, Ogata K, Suzuki M, Honma Y, Momma K, Yatabe K, Tamura T, Kaida K, Miyata N, et al.
    Source:
      NEUROMUSCULAR DISORDERS 27:477-480, 2017
    PMID:
      28214267
  13. Author(s):
      Kageyama Y, Kasahara T, Nakamura T, Hattori K, Deguchi Y, Tani M, Kuroda K, Yoshida S, Goto YI, et al.
    Source:
      Int J Neuropsychopharmacol. 21:207-15, 2018
    PMID:
      29040586
  14. Author(s):
      Kubo K, Deguchi K, Nagai T, Ito Y, Yoshida K, Endo T , Benner S , Shan W , Kitazawa A, et al.
    Source:
      JCI Insight 2:e88609, 2017
    PMID:
      28515367
  15. Author(s):
      Liang WC, Uruha A, Suzuki S, Murakami N, Takeshita E, Chen WZ, Jong YJ, Endo Y, Komaki H, et al.
    Source:
      Rheumatology (Oxford). 56(2): 287-293. Feb. 2017.
    PMID:
      27818386
  16. Author(s):
      Miyatake S, Mitsuhashi S, Hayashi YK, Purevjav E, Nishikawa A, Koshimizu E, Suzuki M, Yatabe K, Tanaka Y, et al.
    Source:
      Am J Hum Genet. 100(1):169-178. 2017.
    PMID:
      28017374
  17. Author(s):
      Mori-Yoshimura M, Segawa K, Minami N, Oya Y, Komaki H, Nonaka I, Nishino I, Murata M.
    Source:
      MUSCLE & NERVE 55:465-469, 2017
    PMID:
      27500519
  18. Author(s):
      Mukai M, Nagata E, Mizuma A, Yamano M, Sugaya K, Nishino I, Goto YI, Takizawa S.
    Source:
      Intern Med. 56(1):95-99. 2017.
    PMID:
      28050007
  19. Author(s):
      Nagata Y, Bundo M, Sugiura S, Kamita M, Ono M, Hattori K, Yoshida S, Goto YI, Urakami K, et al.
    Source:
      Mol Med Rep. 16:3034-40, 2017;
    PMID:
      28714010
  20. Author(s):
      Nakamori M, Hamanaka K, Thomas JD, Wang ET, Hayashi YK, Takahashi MP, Swanson MS, Nishino I, Mochizuki H.
    Source:
      CELL REPORTS 21:1240-1252, 2017
    PMID:
      29091763
  21. Author(s):
      Nakamura K, Hamaguchi T, Sakai K, Noto D, Ono K, Hayashi YK, Nishino I, Yamada M.
    Source:
      Neuromuscul Disord. 27(2):183-184. 2017.
    PMID:
      27919547
  22. Author(s):
      Nishikawa A, Mitsuhashi S, Miyata N, Nishino I.
    Source:
      J Med Genet. 54(2):104-110. 2017.
    PMID:
      27600705
  23. Author(s):
      Noguchi E, Uruha A, Suzuki S, Hamanaka K, Ohnuki Y, Tsugawa J, Watanabe Y, Nakahara J, Shiina T, et al.
    Source:
      JAMA NEUROLOGY 74:992-999, 2017
    PMID:
      28586844
  24. Author(s):
      Ogawa S, Koga N, Hattori K, Matsuo J, Ota M, Hori H, Sasayama D, Teraishi T, Ishida I, et al.
    Source:
      J Psychiatr Res. 96:23-32, 2018
    PMID:
      28950111
  25. Author(s):
      Oguri M, Saito Y, Okazaki T, Matsumura W, Ohno K, Togawa M, Fukuda C, Saito Y, Nishino I, et al.
    Source:
      BRAIN & DEVELOPMENT 39:617-620, 2017
    PMID:
      28318780
  26. Author(s):
      Okubo M, Goto K, Komaki H, Nakamura H, Mori-Yoshimura M, Hayashi YK, Mitsuhashi S, Noguchi S, Kimura E, et al.
    Source:
      ORPHANET JOURNAL OF RARE DISEASES 12:149-149, 2017
    PMID:
      28859693
  27. Author(s):
      Sasayama D, Hattori K, Ogawa S, Yokota Y, Matsumura R, Teraishi T, Hori H, Ota M, Yoshida S, et al.
    Source:
      Hum Mol Genet. 26(1):44-51. 2017.
    PMID:
      28031287
  28. Author(s):
      Suzuki S, Uruha A, Suzuki N, Nishino I.
    Source:
      AUTOIMMUNITY REVIEWS 16:693-700, 2017
    PMID:
      28479486
  29. Author(s):
      Takeshita E, Minami N, Minami K, Suzuki M, Awashima T, Ishiyama A, Komaki H, Nishino I, Sasaki M.
    Source:
      NEUROMUSCULAR DISORDERS 27:569-573, 2017
    PMID:
      28434908
  30. What is the third serological marker associated with immune-mediated necrotizing myopathy?
    Author(s):
      Tanaka T, Suzuki S, Nishino I, Hamaguchi Y, Fujimoto T.
    Source:
      Scand J Rheumatol. 9:1-2. 2017.
    PMID:
      28067601
  31. Author(s):
      Thomas JD, Sznajder LJ, Bardhi O, Aslam FN, Anastasiadis ZP, Scotti MM, Nishino I, Nakamori M, Wang ET, et al.
    Source:
      GENES & DEVELOPMENT 31:1122-1133, 2017
    PMID:
      28698297
  32. A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.
    Author(s):
      Tsunoda K, Yamashita T, Motokura E, Takahashi Y, Sato K, Takemoto M, Hishikawa N, Ohta Y, Nishikawa A, et al.
    Source:
      J Neurol Sci. 373(2017):254-257. 2017.
    PMID:
      28131200
  33. Author(s):
      Uruha A, Nishikawa A, Tsuburaya RS, Hamanaka K, Kuwana M, Watanabe Y, Suzuki S, Suzuki N, Nishino I.
    Source:
      Neurology. 88(5):493-500. 2017.
    PMID:
      28039312
  34. Author(s):
      Uruha A, Suzuki S, Nishino I.
    Source:
      JOURNAL OF CLINICAL & EXPERIMENTAL NEUROIMMUNOLOGY 8:302-312, 2017
    DOI:
      10.1111/cen3.12419
  35. Author update: Sarcoplasmic MxA expression: A valuable marker of dermatomyositis
    Author(s):
      Uruha A, Suzuki S, Nishino I.
    Source:
      NEUROLOGY 89:215-215, 2017
    PMID:
      28696934
  36. Author(s):
      Yokota M, Hatakeyama H, Ono Y, Kanazawa M, Goto Y.
    Source:
      Cell Death Dis. 8(1):e2551. 2017.
    PMID:
      28079893
  37. Author(s):
      Yoon HS, Hattori K, Ogawa S, Sasayama D, Ota M, Teraishi T, Kunugi H.
    Source:
      J Clin Psychiatry. 78:e947-e56, 2017
    PMID:
      28749090
  38. Author(s):
      Zhu W, Mitsuhashi S, Yonekawa T, Noguchi S, Huei JCY, Nalini A, Preethish-Kumar V, Yamamoto M, Murakata K, et al.
    Source:
      J Hum Genet. 62(2):159-166. 2017.
    PMID:
      27829678
  39. 自己免疫性甲状腺疾患とシェーグレン症候群を合併している慢性ミオパチー型筋サルコイドーシスの1例:症例報告及び筋サルコイドーシス自験例の検討
    Author(s):
      磯部 隆,森まどか,大矢 寧,齊藤祐子,村田美穂,西野一三,高橋祐二.
    Source:
      臨床神経学 57:220-224, 2017
    DOI:
      10.5692/clinicalneurol.cn-001012
  40. 顕著な左右非対称性の下肢遠位優位の筋委縮を呈したネマリンミオパチーの2症例
    Author(s):
      水野 由輝郎,森 まどか,大矢 寧,西川 敦子,西野 一三,髙橋 祐二.
    Source:
      臨床神経学 57:691-697, 2017
    DOI:
      10.5692/clinicalneurol.cn-001024
  41. 筋ジストロフィーとの鑑別を要した,慢性経過の小児期発症抗HMGCR(3-hydroxy-3-methyl-glutaryl-CoA reductase) 抗体陽性懐死性ミオパチーの1例
    Author(s):
      濵 由香,森まどか,小牧宏文,鈴木重明,上阪 等,西野一三,髙橋祐二.
    Source:
      臨床神経学 57:567-572, 2017
    DOI:
      10.5692/clinicalneurol.cn-001040

NCNPの2016年の発表、掲載論文に関する検索結果

Search results

Item: 33

No. Publication
  1. Author(s):
      Aizawa E, Tsuji H, Asahara T, Takahashi T, Teraishi T, Yoshida S, Ota M, Koga N, Hattori K, et al.
    Source:
      J Affect Disord. 202:254-7. 2016.
    PMID:
      27288567
  2. Author(s):
      Furuta M, Sumi-Akamaru H, Takahashi MP, Hayashi YK, Nishino I, Mochizuki H.
    Source:
      Neuromuscul Disord. 26(9):593-597. 2016.
    PMID:
      27220833
  3. Author(s):
      Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I.
    Source:
      Neuromuscul Disord. 26(4-5):300-308. Apr-May. 2016
    PMID:
      27061275
  4. Muscle from a 20-week-old myotubular myopathy fetus is not myotubular.
    Author(s):
      Hamanaka K, Inami I, Wada T, Mitsuhashi S, Noguchi S, Hayashi YK, Nishino I.
    Source:
      Neuromuscul Disord. 26(3):234-235. 2016
    PMID:
      26898940
  5. Author(s):
      Hatakeyama H, Goto Y.
    Source:
      Stem Cells. 34(4):801-808. 2016.
    PMID:
      26850516
  6. Author(s):
      Hori H, Sasayama D, Teraishi T, Yamamoto N, Nakamura S, Ota M, Hattori K, Kim Y, Higuchi T, et al.
    Source:
      Sci Rep. 6:18776. 2016.
    PMID:
      26728011
  7. Author(s):
      Ikeda K, Mori-Yoshimura M, Yamamoto T, Sonoo M, Suzuki S, Kondo Y, Nakamura H, Mitsuhashi K, Maeda MH, et al.
    Source:
      J Clin Neuromuscul Dis. 17(4):197-206. 2016.
    PMID:
      27224434
  8. Author(s):
      Inoue T, Murakami N, Ayabe T, Oto Y, Nishino I, Goto YI, Koga Y, Sakuta R.
    Source:
      J Clin Endocrinol Metab. 101(5):1924-6. 2016.
    PMID:
      26885883
  9. Author(s):
      Kim Y, Koide R, Isozaki E, Goto Y.
    Source:
      Neurol Clin Neurosci 4(1):34-35. 2016.
    DOI:
      10.1111/ncn3.12033
  10. Author(s):
      Lee JM, Noguchi S.
    Source:
      Int J Mol Sci. 17(11):E1952. 2016.
    PMID:
      27879676
  11. Author(s):
      Liang WC, Chou PC, Hung CC, Su YN, Kan TM, Chen WZ, Hayashi YK, Nishino I, Jong YJ.
    Source:
      J Neurol Sci. 26(3): 234-235. 2016
    PMID:
      26944168
  12. Author(s):
      Ling F, Niu R, Hatakeyama H, Goto Y, Shibata T, Yoshida M.
    Source:
      Mol Biol Cell. 27(5):1684-1693. 2016
    PMID:
      27009201
  13. Author(s):
      Matsubara S, Shimizu T, Komori T, Mori-Yoshimura M, Minami N, Hayashi YK.
    Source:
      Neuromuscul Disord. 26(7):436-440. 2016.
    PMID:
      27209344
  14. Author(s):
      Matsuoka T, Miwa Y, Tajika M, Sawada M, Fujimaki K, Soga T, Tomita H, Uemura S, Nishino I, et al.
    Source:
      Mol Genet Metab Rep. 9(2016): 98-105. 2016
    PMID:
      27896132
  15. Author(s):
      Miyake N, Fukai R, Ohba C, Chihara T, Miura M, Shimizu H, Kakita A, Imagawa E, Shiina M, et al.
    Source:
      Am J Hum Genet. 99(4):950-961. 2016.
    PMID:
      27666374
  16. Author(s):
      Mizuguchi Y, Hatakeyama H, Sueoka K, Tanaka M, Goto Y.
    Source:
      Mitochondrion. 34:43-48. 2017.
    PMID:
      28093354
  17. Author(s):
      Narumi S, Natori T, Miyazawa H, Kato T, Yonezawa H, Nishino I, Nakamura M, Sano A, Terayama Y.
    Source:
      Neurology and Clinical Neuroscience. 4(3):115-117. 2016.
    DOI:
      10.1111/ncn3.12042
  18. Author(s):
      Ninomiya-Baba M, Matsuo J, Sasayama D, Hori H, Teraishi T, Ota M, Hattori K, Noda T, Ishida I, et al.
    Source:
      Acta Neuropsychiatr. 7:1-10. 2016
    PMID:
      27923415
  19. Author(s):
      Nishikawa A, Mori-Yoshimura M, Segawa K, Hayashi YK, Takahashi T, Saito Y, Nonaka I, Krahn M, Levy N, et al.
    Source:
      Muscle Nerve. 53(3):394-401. 2016.
    PMID:
      26088049
  20. HLA-DRB1 alleles in Immune-mediated necrotizing myopathy.
    Author(s):
      Ohnuki Y, Suzuki S, Shiina T, Uruha A, Watanabe Y, Suzuki S, Izumi S, Nakahara J, Hamanaka K, et al.
    Source:
      Neurology. 87(18):1954-1955. 2016.
    PMID:
      27581220
  21. Author(s):
      Okubo M, Minami N, Goto K, Goto YI, Noguchi S, Mitsuhashi S, Nishino I.
    Source:
      J Hum Genet. 61(6):483-9. 2016.
    PMID:
      26911353
  22. Author(s):
      Ota M, Hori H, Sato N, Yoshida F, Hattori K, Teraishi T, Kunugi H.
    Source:
      Psychiatry Clin Neurosci. 70(11):498-506. 2016.
    PMID:
      27488254
  23. Author(s):
      Setoyama D, Kato TA, Hashimoto R, Kunugi H, Hattori K, Hayakawa K, Sato-Kasai M, Shimokawa N, Kaneko S, et al.
    Source:
      PLoS One. 11(12):e0165267. 2016.
    PMID:
      27984586
  24. Author(s):
      Sugie K, Yoshizawa H, Onoue K, Nakanishi Y, Eura N, Ogawa M, Nakano T, Sakaguchi Y, Hayashi YK, et al.
    Source:
      Neuropathology. 36(6): 561-565. 2016.
    PMID:
      27145725
  25. Author(s):
      Sumida K, Inoue K, Takanashi J, Sasaki M, Watanabe K, Suzuki M, Kurahashi H, Omata T, Tanaka M, et al.
    Source:
      Brain Dev. 38(6):571-80. 2016.
    PMID:
      26774704
  26. Author(s):
      Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata KY, Inamori Y, Matsui N, Kimura E, Kusaka H, et al.
    Source:
      Orphanet J Rare Dis. 11(1):146. 2016.
    PMID:
      27821140
  27. Author(s):
      Takayama K, Mitsuhashi S, Shin JY, Tanaka R, Fujii T, Tsuburaya R, Mukaida S, Noguchi S, Nonaka I, et al.
    Source:
      Neuromuscul Disord. 26(9):604-609. 2016.
    PMID:
      27460346
  28. Author(s):
      Termglinchan T, Hisamatsu S, Ohmori J, Suzumura H, Sumitomo N, Imataka G, Arisaka O, Murakami N, Minami N, et al.
    Source:
      Neurol Genet. 2(5): e95. eCollection. Oct. 2016
    PMID:
      27660820
  29. Author(s):
      Uezumi A, Nakatani M, Ikemoto-Uezumi M, Yamamoto N, Morita M, Yamaguchi A, Yamada H, Kasai T, Masuda S, et al.
    Source:
      Stem Cell Reports. 7(2):263-278. 2016.
    PMID:
      27509136
  30. Perifascicular necrosis in anti-synthetase syndrome beyond anti-Jo-1.
    Author(s):
      Uruha A, Suzuki S, Suzuki N, Nishino I.
    Source:
      Brain. 139(Pt 9):e50. 2016.
    PMID:
      27267378
  31. Author(s):
      Van den Boogaard ML, Lemmers RJ, Balog J, Wohlgemuth M, Auranen M, Mitsuhashi S, van der Vliet PJ, Straasheijm KR, van den Akker RF, et al.
    Source:
      Am J Hum Genet. 98(5):1020-1029. 2016.
    PMID:
      27153398
  32. Author(s):
      Watanabe Y, Uruha A, Suzuki S, Nakahara J, Hamanaka K, Takayama K, Suzuki N, Nishino I.
    Source:
      J Neurol Neurosurg Psychiatry. 87(10):1038-1044. 2016.
    PMID:
      27147697
  33. DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
    Author(s):
      Zaha K, Matsumoto H, Itoh M, Saitsu H, Kato K, Kato M, Ogata S, Murayama K, Kishita Y, et al.
    Source:
      Clin Genet. 90(5):472-474. 2016.
    PMID:
      27301544

NCNPの2015年の発表、掲載論文に関する検索結果

Search results

Item: 36

No. Publication
  1. Author(s):
      Dong M, Noguchi S, Endo Y, Hayashi YK, Yoshida S, Nonaka I, Nishino I.
    Source:
      Neurology. 84(3).273-279. 2015.
    PMID:
      25503980
  2. Author(s):
      Endo Y, Dong M, Noguchi S, Ogawa M, Hayashi YK, Kuru S, Sugiyama K, Nagai S, Ozasa S, et al.
    Source:
      Neurol Genet. 1(4): e33. 2015.
    PMID:
      27066570
  3. Author(s):
      Endo Y, Noguchi S, Hara Y, Hayashi YK, Motomura K, Miyatake S, Murakami N, Tanaka S, Yamashita S, et al.
    Source:
      HUMAN MOLECULAR GENETICS. 24(3):637-648. 2015.
    PMID:
      25227914
  4. Author(s):
      Fukasawa T, Kubota T, Maruyama S, Saito Y, Itoh M, Kakita A, Sugai K, Otsuki T, Kato M, et al.
    Source:
      Pediatr Int. 57:472-475. 2015.
    PMID:
      26012518
  5. Author(s):
      Furuta A, Kikuchi H, Fujita H, Yamada D, Fujiwara Y, Kabuta T, Nishino I, Wada K, Uchiyama Y.
    Source:
      Am J Pathol. 185(6):1713-1723. 2015.
    PMID:
      25998250
  6. Author(s):
      Gage BK, Asadi A, Baker RK, Webber TD, Wang R, Itoh M, Hayashi M, Miyata R, Akashi T, et al.
    Source:
      PLoS One. 10(12):e0144100. 2015.
    PMID:
      26633894
  7. Author(s):
      Hatakeyama H, Katayama A, Komaki H, Nishino I, Goto Y.
    Source:
      Acta Neuropathol Commun. 3:52. 2015.
    PMID:
      26297375
  8. Author(s):
      Hattori K, Ota M, Sasayama D, Yoshida S, Matsumura R, Miyakawa T, Yokota Y, Yamaguchi S, Noda T, et al.
    Source:
      Sci Rep. 17:11412. 2015.
    PMID:
      26081315
  9. Author(s):
      Ito Y, Inoue N, Inoue YU, Nakamura S, Matsuda Y, Inagaki M, Ohkubo T, Asami J, Terakawa YW, et al.
    Source:
      Neurobiol Dis 80:1-14. 2015
    PMID:
      25959061
  10. Author(s):
      Izumi R, Warita H, Niihori T, Takahashi T, Tateyama M, Suzuki N, Nishiyama A, Shirota M, Funayama R, et al.
    Source:
      Neurol Genet. 1(3): e23. 2015
    PMID:
      27066560
  11. Author(s):
      Kawasaki Y, Naba I, Azuma S, Yaka K, Moriya M, Nakano M, Nishino I, Tatsumi C.
    Source:
      Neurology and Clinical Neuroscience. 3(4):131-133. 2015.
    DOI:
      10.1111/ncn3.162
  12. Author(s):
      Kawase K, Nishino I, Sugimoto M, Kouwaki M, Koyama N, Yokochi K.
    Source:
      BRAIN & DEVELOPMENT. 37(2):265-269. 2015.
    PMID:
      24787270
  13. Author(s):
      Kawase K, Nishino I, Sugimoto M, Togawa T, Sugiura T, Kouwaki M, Kibe T, Koyama N, Yokochi K.
    Source:
      Brain Dev. 37(9):887-890. 2015.
    PMID:
      25721947
  14. Author(s):
      Kida H, Sano K, Yorita A, Miura S, Ayabe M, Hayashi YK, Nishino I, Taniwaki T.
    Source:
      Neurology and Clinical Neuroscience. 3(4):150-152. 2015.
    DOI:
      10.1111/ncn3.175
  15. Author(s):
      Kimura H, Tsuboi D, Wang C, Kushima I, Koide T, Ikeda M, Iwayama Y, Toyota T, Yamamoto N, et al.
    Source:
      Schizophr Bull. 41:744-753. 2015.
    PMID:
      25332407
  16. Author(s):
      Kunugi H,Hori H, Ogawa S.
    Source:
      Psychiatry and Clinical Neurosciences. 69(10):597-608. 2015.
    PMID:
      25825158
  17. Author(s):
      Liang WC, Zhu WH, Mitsuhashi S, Noguchi S, Sacher M, Ogawa M, Shin HH, Jong YJ, Nishino I.
    Source:
      Skeletal Muscle. 5:29.eCollection. 2015.
    PMID:
      26322222
  18. Author(s):
      Matsuda C, Kiyosue K, Nishino I, Hayashi YK.
    Source:
      PLoS Curr. pii:ecurrents.md.5865add2d766f39a0e0411d38a7ba09c. 2015.
    PMID:
      26579332
  19. Author(s):
      Montassir H, Maegaki Y, Murayama K, Yamazaki T, Kohda M, Ohtake A, Iwasa H, Yatsuka Y, Okazaki Y, et al.
    Source:
      Brain Dev. 37:719-724. 2015.
    PMID:
      25466440
  20. Congenital autophagic vacuolar myopathy is allelic to X-linked myopathy with excessive autophagy.
    Author(s):
      Munteanu I, Ramachandran N, Ruggieri A, Awaya T, Nishino I, Minassian BA.
    Source:
      Neurology. 84(16):1714-1716. 2015.
    PMID:
      25817839
  21. Author(s):
      Ogawa S, Hattori K, Sasayama D, Yokota Y, Matsumura R, Matsuo J, Ota M, Hori H, Teraishi T, et al.
    Source:
      Sci Rep. 5:7796. 2015.
    PMID:
      25589364
  22. Author(s):
      Ohsawa N, Koebis M, Mitsuhashi H, Nishino I, Ishiura S.
    Source:
      GENES TO CELLS 20(2). 121-134. 2015.
    PMID:
      25403273
  23. Author(s):
      Omata T, Nagai J, Shimbo H, Koizume S, Miyagi Y, Kurosawa K, Yamashita S, Osaka H, Inoue K.
    Source:
      Brain Dev. 38(6):581-4. 2015.
    PMID:
      26725305
  24. Author(s):
      Osaka H, Inoue K.
    Source:
      Expert Opinion on Orphan Drugs. 3:1447-1459. 2015.
    DOI:
      10.1517/21678707.2015.1106315
  25. Author(s):
      Sakai C, Yamaguchi S, Sasaki M, Miyamoto Y, Matsushima Y, Goto Y.
    Source:
      Hum Mut. 36(2):232-9. 2015
    PMID:
      25393721
  26. Author(s):
      Sanmaneechai O, Likasitwattanakul S, Sangruchi T, Nishino I.
    Source:
      Brain Dev. 37(4):459-462. 2015.
    PMID:
      25112543
  27. Author(s):
      Sasayama D, Hori H, Nakamura S, Yamamoto N, Hattori K, Teraishi T, Ota M, Kunugi H.
    Source:
      Horm Metab Res. 47:433-438. 2015
    PMID:
      25011018
  28. Author(s):
      Suzuki S, Nishikawa A, Kuwana M, Nishimura H, Watanabe Y, Nakahara J, Hayashi YK, Suzuki N, Nishino I.
    Source:
      Orphanet J Rare Dis. 10(1):61. 2015.
    PMID:
      25963141
  29. Kyphoscoliosis and easy fatigability in a 14-year-old boy
    Author(s):
      Tanboon J, Hayashi YK, Nishino I, Sangruchi T.
    Source:
      Neuropathology. 35(1).91-3. 2015.
    PMID:
      25168271
  30. 2 Month-Old Male with Hypotonia.
    Author(s):
      Tanboon J, Viravan S, Hayashi YK, Nishino I, Sangruchi T.
    Source:
      Brain Pathol. 25(5):651-652. 2015.
    PMID:
      26276028
  31. Family with centronuclear myopathy as a result of a novel p.R369G DNM2 mutation.
    Author(s):
      Toyooka K, Kubo K, Fujimura H, Sakoda S, Tominaga K, Nishino I.
    Source:
      Neurology and Clinical Neuroscience. 3(4):161-162. 2015.
    DOI:
      10.1111/ncn3.176
  32. Author(s):
      Tsujimura K, Irie K, Nakashima H, Egashira Y, Fukao Y, Fujiwara M, Itoh M, Uesaka M, Imamura T, et al.
    Source:
      Cell Reports. 12:1887-1901. 2015.
    PMID:
      26344767
  33. Author(s):
      Uruha A, Hayashi YK, Oya Y, Mori-Yoshimura M, Kanai M, Murata M, Kawamura M, Ogata K, Matsumura T, et al.
    Source:
      J Neurol Neurosurg Psychiatry. 86(5):483-489. 2015.
    PMID:
      25253871
  34. Author(s):
      Wang CH, Liang WC, Minami N, Nishino I, Jong YJ.
    Source:
      PEDIATRICS AND NEONATOLOGY 56(1).62-65. 2015.
    PMID:
      23597518
  35. Author(s):
      Yokota M, Hatakeyama H, Okabe S, Ono Y, Goto Y.
    Source:
      Hum Mol. Genet. 24:4698-4709. 2015
    PMID:
      26025377
  36. Author(s):
      Zhao Y, Ogawa H, Yonekura SI, Mitsuhashi H, Mitsuhashi S, Nishino I, Toyoshima C, Ishiura S.
    Source:
      Biochim Biophys Acta. 1852(10):2042-2047. 2015.
    PMID:
      26170059

NCNPの2014年の発表、掲載論文に関する検索結果

Search results

Item: 25

No. Publication
  1. Absence of beta-amyloid deposition in the central nervous system of a transgenic mouse model of distal myopathy with rimmed vacuoles
    Author(s):
      Anada RP, Wong KT, Malicdan MC, Goh KJ, Hayashi YK, Nishino I, Noguchi S.
    Source:
      AMYLOID. 21(2):138-9. 2014.
    PMID:
      24601867
  2. Author(s):
      Cho A, Hayashi YK, Monma K, Oya Y, Noguchi S, Nonaka I, Nishino I.
    Source:
      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 85(8):914-917. 2014.
    PMID:
      24027297
  3. Author(s):
      Fujii T, Hayashi S, Kawamura N, Higuchi MA, Tsugawa J, Ohyagi Y, Hayashi YK, Nishino I, Kira JI.
    Source:
      JOURNAL OF THE NEUROLOGICAL SCIENCES. 343(1-2):206-10. 2014.
    PMID:
      24928078
  4. Author(s):
      Fujii T, Hori H, Ota M, Hattori K, Teraishi T, Sasayama D, Yamamoto N, Higuchi T, Kunugi H.
    Source:
      Psychoneuroendocrinology. 42:89-97. 2014.
    PMID:
      24636505
  5. Author(s):
      Goto M, Komaki H, Saito T, Saito Y, Nakagawa E, Sugai K, Sasaki M, Nishino I, Goto Y.
    Source:
      Brain Dev. 36(2):180-2. 2014.
    PMID:
      23582502
  6. Author(s):
      Goto M, Okada M, Komaki H, Sugai K, Sasaki M, Noguchi S, Nonaka I, Nishino I, Hayashi YK.
    Source:
      ORPHANET JOURNAL OF RARE DISEASES. 9(1):58. 2014
    PMID:
      24755310
  7. Author(s):
      Hori H, Teraishi T, Ota M, Hattori K, Matsuo J, Kinoshita Y, Ishida I, Nagashima A, Koga N, et al.
    Source:
      J Affect Disord. 152-154:441-7. 2014.
    PMID:
      24210627
  8. Author(s):
      Hori H, Yamamoto N, Teraishi T, Ota M, Fujii T, Sasayama D, Matsuo J, Kinoshita Y, Hattori K, et al.
    Source:
      J Affect Disord. 158:90-6. 2014.
    PMID:
      24655771
  9. GNE myopathy: New name and new mutation nomenclature
    Author(s):
      Huizing M, Carrillo-Carrasco N, Malicdan MC, Noguchi S, Gahl WA, Mitrani-Rosenbaum S, Argov Z, Nishino I.
    Source:
      NEUROMUSCULAR DISORDERS. 24(5):387-389. 2014.
    PMID:
      24685570
  10. Author(s):
      Kajino S, Ishihara K, Goto K, Ishigaki K, Noguchi S, Nonaka I, Osawa M, Nishino I, Hayashi YK.
    Source:
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NCNPの2013年の発表、掲載論文に関する検索結果

Search results

Item: 23

No. Publication
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  3. An association analysis of the cardiomyopathy-associated 5 (CMYA5) gene with schizophrenia in a Japanese population
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  8. Additional evidence that the ryanodine receptor gene (RYR1) causes malignant hyperthermia and severe skeletal malformations
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  10. Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy
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NCNPの2012年の発表、掲載論文に関する検索結果

Search results

Item: 34

No. Publication
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  15. Myotonic dystrophy type 2 is rare in the Japanese population
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  29. Teaching NeuroImages: unilateral arm and contralateral leg amyotrophy in FSHD: unusual presentation
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NCNPの2011年の発表、掲載論文に関する検索結果

Search results

Item: 21

No. Publication
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      Fujii T, Uchiyama H, Yamamoto N, Hori H, Tatsumi M, Ishikawa M, Arima K, Higuchi T, Kunugi H.
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  20. Lobulated fibers in a patient with 46-year history of limb-girdle muscle weakness
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NCNPの2010年の発表、掲載論文に関する検索結果

Search results

Item: 11

No. Publication
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      Amagane H, Watanabe Y, Kaneko N, Nunokawa A, Muratake T, Ishiguro H, Arinami T, Ujike H, Inada T, et al.
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      Seizure. 19(5):274-9. 2010.
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      20452788
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      World J Biol Psychiatry. 11(2 Pt 2):431-8. 2010.
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      19353385
  4. Author(s):
      Honda S, Hayashi S, Imoto I, Toyama J, Okazawa H, Nakagawa E, Goto Y, Inazawa J.
    Source:
      J Hum Genet. 55(9):590-9. 2010.
    PMID:
      20613765
  5. Author(s):
      Kim H, Cho A, Lim BC, Kim MJ, Kim KJ, Nishino I, Hwang YS, Chae JH.
    Source:
      Muscle Nerve. 41(6):879-82. 2010.
    PMID:
      20513107
  6. Author(s):
      Mimaki M, Hatakeyama H, Komaki H, Yokoyama M, Arai H, Kirino Y, Suzuki T, Nishino I, Nonaka I, et al.
    Source:
      Ann Neurol. 68(6):845-54. 2010.
    PMID:
      21194154
  7. Author(s):
      Mitsuhashi H, Hayashi YK, Matsuda C, Noguchi S, Wakatsuki S, Araki T, Nishino I.
    Source:
      J Cell Sci. 123(Pt 22):3893-900. 2010.
    PMID:
      20980393
  8. Author(s):
      Osaka H, Hamanoue H, Yamamoto R, Nezu A, Sasaki M, Saitsu H, Kurosawa K, Shimbo H, Matsumoto N, et al.
    Source:
      Ann Neurol. 68(2):250-4. 2010.
    PMID:
      20695017
  9. Author(s):
      Ozeki Y, Fujii K, Kurimoto N, Yamada N, Okawa M, Aoki T, Takahashi J, Ishida N, Horie M, et al.
    Source:
      Prog Neuropsychopharmacol Biol Psychiatry. 34(2):401-5. 2010.
    PMID:
      20079791
  10. Author(s):
      Takebayashi M, Hashimoto R, Hisaoka K, Tsuchioka M, Kunugi H.
    Source:
      J Neural Transm. 117(9):1119-22. 2010.
    PMID:
      20690032
  11. Author(s):
      Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I.
    Source:
      Acta Neuropathol. 119(4):481-6. 2010.
    PMID:
      20179953

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