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NCNPの2022年の発表、掲載論文に関する検索結果

Search results

Item: 3

No. Publication
  1. Author(s):
      Araki W, Kanemaru K, Hattori K, Tsukamoto T, Saito Y, Yoshida S, Takano H, Sakata M, Yokoi Y, et al.
    Source:
      Aging Clin Exp Res.
    PMID:
      34283410
  2. Author(s):
      Tabata K, Ishiyama A, Nakamura Y, Sasaki M, Inoue K, Goto YI.
    Source:
      Eur J Med Genet.
    PMID:
      35134569
  3. Author(s):
      Kawazoe T, Tobisawa S, Sugaya K, Uruha A, Miyamoto K, Komori T, Goto YI, Nishino I, Yoshihashi H, et al.
    Source:
      Intern Med
    PMID:
      34433719

NCNPの2021年の発表、掲載論文に関する検索結果

Search results

Item: 12

No. Publication
  1. Author(s):
      Chihiro Abe-Hatano,Aritoshi Iida,Shunichi Kosugi,Yukihide Momozawa,Chikashi Terao,Keiko Ishikawa,Mariko Okubo,Yasuo Hachiya,Hiroya Nishida, et al.
    Source:
      AMERICAN JOURNAL OF MEDICAL GENETICS Part A. 185(5):1468-1480, 2021
    PMID:
      33624935
  2. Author(s):
      Saito K, Hattori K, Hidese S, Sasayama D, Miyakawa T, Matsumura R, Tatsumi M, Yokota Y, Ota M, et al.
    Source:
      Metabolites.
    PMID:
      33923144
  3. Author(s):
      Idemoto K, Niitsu T, Hata T, Ishima T, Yoshida S, Hattori K, Horai T, Otsuka I, Yamamori H, et al.
    Source:
      Psychiatry Res.
    PMID:
      33990070
  4. Author(s):
      Omori W, Kano K, Hattori K, Kajitani N, Okada-Tsuchioka M, Boku S, Kunugi H, Aoki J, Takebayashi M.
    Source:
      Int J Neuropsychopharmacol.
    PMID:
      34214158
  5. Author(s):
      Kageyama Y, Deguchi Y, Hattori K, Yoshida S, Goto YI, Inoue K, Kato T.
    Source:
      Brain Behav.
    PMID:
      33599392
  6. Author(s):
      Ishigaki H, Sato N, Kimura Y, Takeshita E, Komaki H, Chiba E, Shigemoto Y, Goto YI, Mori-Yoshimura M, et al.
    Source:
      Brain Dev.
    PMID:
      34049744
  7. Author(s):
      Bonora E, Chakrabarty S, Kellaris G, Tsutsumi M, Bianco F, Bergamini C, Ullah F, Isidori F, Liparulo I, et al.
    Source:
      Brain
    PMID:
      33855352
  8. Author(s):
      Kumutpongpanich T, Ogasawara M, Ozaki A, Ishiura H, Tsuji S, Minami N, Hayashi S, Noguchi S, Iida A, et al.
    Source:
      JAMA Neurol
    PMID:
      34047774
  9. Author(s):
      Toki T, Shimizu-Motohashi Y, Komaki H, Takeshita E, Ishiyama A, Saito T, Mori-Yoshimura M, Sumitomo N, Hirasawa-Inoue A, et al.
    Source:
      Pediat Neurol 114: 1-4, 2021
    PMID:
      33189023
  10. Author(s):
      Abe-Hatano C, Iida A, Kosugi S, Momozawa Y, Terao C, Ishikawa K, Okubo M, Hachiya Y, Nishida H, et al.
    Source:
      Am J Med Genet Part A 185: 1468-1480, 2021
    PMID:
      33624935
  11. Author(s):
      Raveney BJE, Sato W, Takewaki D, Zhang C, Kanazawa T, Lin Y, Okamoto T, Araki M, Kimura Y, et al.
    Source:
      Proc Natl Acad Sci U S A. 2021 Mar 16; 118(11): e2021818118, 2021
    PMID:
      33836594
  12. Author(s):
      Hidese S. Hattori K. Sasayama D. Tsumagari T. Miyakawa T. Matsumura R. Yokota Y. Ishida I. Matsuo J. et al.
    Source:
      Frontiers in Pharmacology, 11:594394, 2021
    PMID:
      33708113

NCNPの2020年の発表、掲載論文に関する検索結果

Search results

Item: 12

No. Publication
  1. Author(s):
      Nagao T, Shintani Y, Hayashi T, Koika H, Kato H, Nishida Y, Yamazaki S, Tsukamoto O, Yashirogi S, et al.
    Source:
      FASEB J 34:1859-1871, 2020
    PMID:
      31914602
  2. Author(s):
      Miura M, Ishiyama A, Sumitomo N, Takeshita E, Hotohashi Y, Saito T, Komaki H, Nakagawa E, Sasaki M, et al.
    Source:
      Bran Dev 42:581-586, 2020
    PMID:
      32507666
  3. Author(s):
      Tarasaki A, Nakamura M, Urata Y, Hiwatahi H, Yokoyama I, Yasuda T, Onuma T, Wada K, Kaneko S, et al.
    Source:
      J Hum Genet 66: 419-429, 2020
    PMID:
      33040085
  4. Author(s):
      Kobayashi H, Hatakeyama H, Nishimura H, Yokota M, Suzuki S, Tomabechi Y, Shirouzu M, Osada H, Mimaki M, et al.
    Source:
      Nat Chem Bio 17: 335-343, 2021
    PMID:
      33168978
  5. Author(s):
      Hayase Y, Amano S, Hashizume K, Tominaga T, Miyamoto H, Kanno Y, Ueno-Inoue Y, Inoue T, Yamada M, et al.
    Source:
      Acta Neuropathol Commun. 8: 206, 2020
    PMID:
      33256836
  6. Author(s):
      Omori W, Hattori K, Kajitani N, Tsuchioka MO, Boku S, Kunugi H, Okamoto Y, Takebayashi M.
    Source:
      Int J Neuropsychopharmacol 16;23:713-720, 2020
    PMID:
      32671384
  7. Author(s):
      Sasayama D, Hattori K, Yokota Y, Matsumura R, Teraishi T, Yoshida S, Kunugi H.
    Source:
      Neuropsychopharmacol Rep. 40:201-205, 2020
    PMID:
      32426945
  8. Author(s):
      Saito K, Hattori K, Andou T, Satomi Y, Gotou M, Kobayashi H, Hidese S, Kunugi H.
    Source:
      Metabolites. 10:185, 2020
    PMID:
      32384774
  9. Author(s):
      Hidese S, Hattori K, Sasayama D, Tsumagari T, Miyakawa T, Matsumura R, Yokota Y, Ishida I, Matsuo J, et al.
    Source:
      Transl Psychiatry. 10:161, 2020
    PMID:
      32439851
  10. Author(s):
      Ogawa S, Hattori K, Ota M, Hidese S, Miyakawa T, Matsumura R, Yokota Y, Ishida I, Matsuo J, et al.
    Source:
      Psychiatry Clin Neurosci 74:204-210, 2020
    PMID:
      31841251
  11. A novel homoplasmic mitochondrial DNA mutation (m.13376T>C, p.I347T) of MELAS presenting characteristic medial temporal lobe atrophy
    Author(s):
      Sasaki R, Ohta Y, Hatanaka N, Tadokoro K, Nomura E, Shang J, Takemoto M, Hishikawa N, Yamashita T, et al.
    Source:
      J Neurol Sci 408:116460, 2020
    PMID:
      31689606
  12. A novel pathogenic NFIX variant in a Malan syndrome patient associated with hindbrain overcrowding
    Author(s):
      Tabata K, Iida A, Takeshita E, Nakagawa E, Sato N, Sasaki M, Inoue K,Goto YI.
    Source:
      J Neurol Sci 412:116758, 2020
    PMID:
      32193017

NCNPの2019年の発表、掲載論文に関する検索結果

Search results

Item: 20

No. Publication
  1. Author(s):
      Gotoh L, Yamada M, Hattori K, Sasayama D, Noda T, Yoshida S, Kunugi H,Yamada M.
    Source:
      Heliyon 5:e01699, 2019
    PMID:
      31193411
  2. Author(s):
      Hirasawa-Inoue A, Takeshita E, Shimizu-Motohashi Y, Ishiyama A, Saito T, Komaki H, Nakagawa E, Sugai K, Inoue K, et al.
    Source:
      Neuropediatrics 50:387-390, 2019
    PMID:
      31370080
  3. Author(s):
      Iida A, Takano K, Takeshita E, Abe-Hatano C, Hirabayashi S, Inaba Y, Kosugi S, Kamatani Y, Momozawa Y, et al.
    Source:
      Cold Spring Harb Mol Case Stud 5:2019
    PMID:
      31444167
  4. Author(s):
      Inoue M, Uchino S, Iida A, Noguchi S, Hayashi S, Takahashi T, Fujii K, Komaki H, Takeshita E, et al.
    Source:
      Ann Neurol 86:193-202, 2019
    PMID:
      31155743
  5. Author(s):
      Itagaki K, Takebayashi M, Abe H, Shibasaki C, Kajitani N, Okada-Tsuchioka M, Hattori K, Yoshida S, Kunugi H, et al.
    Source:
      Int J Neuropsychopharmacol 22:261-269, 2019
    PMID:
      30715387
  6. Author(s):
      Iwama K, Mizuguchi T, Takeshita E, Nakagawa E, Okazaki T, Nomura Y, Iijima Y, Kajiura I, Sugai K, et al.
    Source:
      J Med Genet 56:396-407, 2019
    PMID:
      30842224
  7. Author(s):
      Kadowaki A, Saga R, Lin Y, Sato W,Yamamura T.
    Source:
      Brain 142:916-931, 2019
    PMID:
      30770703
  8. Author(s):
      Koga N, Ogura J, Yoshida F, Hattori K, Hori H, Aizawa E, Ishida I,Kunugi H.
    Source:
      Transl Psychiatry 9:208, 2019
    PMID:
      31455761
  9. Author(s):
      Mizui T, Hattori K, Ishiwata S, Hidese S, Yoshida S, Kunugi H,Kojima M.
    Source:
      J Psychiatr Res 113:190-198, 2019
    PMID:
      30986693
  10. A unique Japanese CPEO family with a novel homozygous m.14819T>G (p. S25A) substitution
    Author(s):
      Nomura E, Ohta Y, Tadokoro K, Sato K, Sasaki R, Takahashi Y, Yamashita T, Takemoto M, Hishikawa N, et al.
    Source:
      J Neurol Sci 400:145-147, 2019
    PMID:
      30951992
  11. 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:
      Schizophr Res 208:462-464, 2019
    PMID:
      30852115
  12. Author(s):
      Sasayama D, Hattori K,Kunugi H.
    Source:
      Methods Mol Biol 2044:365-376, 2019
    PMID:
      31432426
  13. Author(s):
      Takeshita E, Iida A, Abe-Hatano C, Nakagawa E, Sasaki M, Inoue K,Goto YI.
    Source:
      Hum Genome Var 6:48, 2019
    PMID:
      31645986
  14. Author(s):
      Tsuchimine S, Hattori K, Ota M, Hidese S, Teraishi T, Sasayama D, Hori H, Noda T, Yoshida S, et al.
    Source:
      Neuropsychiatr Dis Treat 15:2221-2230, 2019
    PMID:
      31496705
  15. Author(s):
      Uchino S, Iida A, Sato A, Ishikawa K, Mimaki M, Nishino I,Goto YI.
    Source:
      Hum Genome Var 6:19, 2019
    PMID:
      31016024
  16. 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
  17. Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome
    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
  18. Levels of lysophosphatidic acid in cerebrospinal fluid and plasma of patients with schizophrenia
    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
  19. Reduced Serum and Cerebrospinal Fluid Levels of Autotaxin in Major Depressive Disorder
    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
  20. 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. Efficacy of Prednisolone in Generated Myotubes Derived From Fibroblasts of Duchenne Muscular Dystrophy Patients
    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. A patient-derived iPSC model revealed oxidative stress increases facioscapulohumeral muscular dystrophy-causative DUX4
    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. Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552∗)
    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. Interpretation of acid α-glucosidase activity in creatine kinase elevation: A case of Becker muscular dystrophy
    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. Quantification of lectin fluorescence in GNE myopathy muscle biopsies
    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. Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance (SLONM-MGUS): An alternative treatment using cyclophosphamide-thalidomide-dexamethasone (CTD) regimen
    Author(s):
      Kumutpongpanich T, Owattanapanich W, Tanboon J, Nishino I, Boonyapisit K.
    Source:
      NEUROMUSCULAR DISORDERS 28:610-613, 2018
    PMID:
      29910095
  9. A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy
    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. Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy
    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. NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy
    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. Genetic and functional analysis of the RYR1 mutation p.Thr84Met revealed a susceptibility to malignant hyperthermia
    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. The relationship between circulating mitochondrial DNA and inflammatory cytokines in patients with major depression
    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. CO2-sensitive tRNA modification associated with human mitochondrial disease
    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. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights
    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. A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation
    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. 13 C-phenylalanine breath test and serum biopterin in schizophrenia, bipolar disorder and major depressive disorder
    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. Low cocaine- and amphetamine-regulated transcript (CART) peptide levels in human cerebrospinal fluid of major depressive disorder (MDD) patients
    Author(s):
      Yoon HS, Hattori K, Sasayama D, Kunugi H.
    Source:
      JOURNAL OF AFFECTIVE DISORDERS 232:134-138, 2018
    PMID:
      29486339
  23. Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect
    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:
      JOURNAL OF THE NEUROLOGICAL SCIENCES. 340(1-2):94-98. 2014.
    PMID:
      24642510
  11. Author(s):
      Miyashita A,Wen Y,Kitamura N,Matsubara E,Kawarabayashi T,Shoji M,Tomita N, Furukawa K,Arai H, et al.
    Source:
      Journal of Alzheimer's Disease. 41(4):1031-1038. 2014.
    PMID:
      24762945
  12. Author(s):
      Miyatake S, Koshimizu E, Hayashi YK, Miya K, Shiina M, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, et al.
    Source:
      NEUROMUSCULAR DISORDERS. 24(7):642-647. 2014.
    PMID:
      24852243
  13. Author(s):
      Mori-Yoshimura M, Hayashi YK, Yonemoto N, Nakamura H, Murata M, Takeda SI, Nishino I, Kimura E.
    Source:
      ORPHANET JOURNAL OF RARE DISEASES. 9:150. 2014.
    PMID:
      25303967
  14. Author(s):
      Mori-Yoshimura M, Oya Y, Yajima H, Yonemoto N, Kobayashi Y, Hayashi YK, Noguchi S, Nishino I, Murata M.
    Source:
      NEUROMUSCULAR DISORDERS. 24(5):380-386. 2014.
    PMID:
      24656604
  15. A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency
    Author(s):
      Murata KY, Sugie H, Nishino I, Kondo T, Ito H.
    Source:
      Muscle Nerve. 49(2):295-6. 2014.
    PMID:
      23966064
  16. Author(s):
      Noguchi S, Ogawa M, Kawahara G, Malicdan MC, Nishino I.
    Source:
      MOLECULAR THERAPY-NUCLEIC ACIDS. 3:e171. 2014
    PMID:
      24959844
  17. Author(s):
      Ogawa S, Fujii T, Koga N, Hori H, Teraishi T, Hattori K, Noda T, Higuchi T, Motohashi N, et al.
    Source:
      Journal of Clinical Psychiatry. 75(9):e906-e915. 2014.
    PMID:
      25295433
  18. Author(s):
      Ohnuki Y, Takahashi K, Iijima E, Takahashi W, Suzuki S, Ozaki Y, Kitao R, Mihara M, Ishihara T, et al.
    Source:
      Inter Med. 53:1365-1369. 2014
    PMID:
      24930659
  19. Author(s):
      Ojima K, Ono Y, Hata S, Noguchi S, Nishino I, Sorimachi H.
    Source:
      GENES TO CELLS. 19(11):830-841. 2014.
    PMID:
      25252031
  20. Author(s):
      Saitsu H, Tohyama J, Walsh T, Kato M, Kobayashi Y, Lee M, Tsurusaki Y, Miyake N, Goto YI, et al.
    Source:
      JOURNAL OF HUMAN GENETICS. 59(10):581-3. 2014.
    PMID:
      25102098
  21. Author(s):
      Sasayama D, Hori H, Yamamoto N, Nakamura S, Teraishi T, Tatsumi M, Hattori K, Ota M, Higuchi T, et al.
    Source:
      J Psychiatr Res. 50:79-83. 2014.
    PMID:
      24373612
  22. Author(s):
      Sugiura T, Kawaguchi Y, Goto K, Hayashi Y, Gono T, Furuya T, Nishino I, Yamanaka H.
    Source:
      PLoS One. 9(3):e90019. 2014.
    PMID:
      24632671
  23. Author(s):
      Suzuki S, Yonekawa T, Kuwana M, Hayashi YK, Okazaki Y, Kawaguchi Y, Suzuki N, Nishino I.
    Source:
      JOURNAL OF NEUROIMMUNOLOGY. 274(1-2):202-208. 2014.
    PMID:
      25064497
  24. Author(s):
      Yonekawa T, Malicdan MC, Cho A, Hayashi YK, Nonaka I, Mine T, Yamamoto T, Nishino I, Noguchi S.
    Source:
      BRAIN. 137(10):2670-2679. 2014.
    PMID:
      25062695
  25. Author(s):
      Yuen M, Sandaradura SA, Dowling JJ, Kostyukova AS, Moroz N, Quinlan KG, Lehtokari VL, Ravenscroft G, Todd EJ, et al.
    Source:
      THE JOURNAL OF CLINICAL INVESTIGATION. 124(11):4693-4708. 2014.
    PMID:
      25250574

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
  1. Author(s):
      Balan S, Yamada K, Iwayama Y, Toyota T, Ohnishi T, Maekawa M, Toyoshima M, Iwata Y, Suzuki K, et al.
    Source:
      Gene. 526(2):246-50. 2013.
    PMID:
      23747400
  2. Author(s):
      Chou PC, Liang WC, Nonaka I, Mitsuhashi S, Nishino I, Jong YJ.
    Source:
      Brain Dev. 35(7):686-9. 2013.
    PMID:
      23102861
  3. An association analysis of the cardiomyopathy-associated 5 (CMYA5) gene with schizophrenia in a Japanese population
    Author(s):
      Furukawa M, Tochigi M, Otowa T, Arinami T, Inada T, Ujike H, Watanabe Y, Iwata N, Itokawa M, et al.
    Source:
      Psychiatr Genet. 23(4):179-80. 2013.
    PMID:
      23528614
  4. Author(s):
      Gupta VA, Ravenscroft G, Shaheen R, Todd EJ, Swanson LC, Shiina M, Ogata K, Hsu C, Clarke NF, et al.
    Source:
      Am J Hum Genet. 93(6):1108-17. 2013.
    PMID:
      24268659
  5. Author(s):
      Hida A, Kitamura S, Ohsawa Y, Enomoto M, Katayose Y, Motomura Y, Moriguchi Y, Nozaki K, Watanabe M, et al.
    Source:
      Sci Rep. 3:2074. 2013.
    PMID:
      23797865
  6. Author(s):
      Hori H, Teraishi T, Sasayama D, Hattori K, Hashikura M, Higuchi T, Kunugi H.
    Source:
      J Affect Disord. 147(1-3):128-36. 2013.
    PMID:
      23178186
  7. Author(s):
      Ishiyama A, Komaki H, Saito T, Saito Y, Nakagawa E, Sugai K, Itagaki Y, Matsuzaki K, Nakura M, et al.
    Source:
      Brain Dev. 35(7):654-9. 2013.
    PMID:
      23182449
  8. Additional evidence that the ryanodine receptor gene (RYR1) causes malignant hyperthermia and severe skeletal malformations
    Author(s):
      Kakisaka Y, Haginoya K, Takahashi Y, Ochiai T, Fujiwara I, Kikuchi A, Wakusawa K, Kobayashi S, Kikuchi H, et al.
    Source:
      Am J Med Genet A. 161A(1):234-5. 2013.
    PMID:
      23239586
  9. Author(s):
      Kurashige T, Takahashi T, Yamazaki Y, Nagano Y, Kondo K, Nakamura T, Yamawaki T, Tsuburaya R, Hayashi YK, et al.
    Source:
      Neuromuscul Disord. 23(11):911-6. 2013.
    PMID:
      23850239
  10. Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy
    Author(s):
      Matsuura T, Kurosaki T, Omote Y, Minami N, Hayashi YK, Nishino I, Abe K.
    Source:
      J Hum Genet. 58(8):564-5. 2013.
    PMID:
      23677060
  11. Author(s):
      Mitsuhashi S, Nishino I.
    Source:
      Curr Opin Neurol. 26(5):536-43. 2013.
    PMID:
      23945283
  12. Author(s):
      Miyake N, Yano S, Sakai C, Hatakeyama H, Matsushima Y, Shiina M, Watanabe Y, Bartley J, Abdenur JE, et al.
    Source:
      Hum Mutat. 34(3):446-52. 2013.
    PMID:
      23281071
  13. Author(s):
      Mori-Yoshimura M, Oya Y, Hayashi YK, Noguchi S, Nishino I, Murata M.
    Source:
      Neuromuscul Disord. 23(1):84-8. 2013.
    PMID:
      23127962
  14. Author(s):
      Motoki T, Fukuda M, Nakano T, Matsukage S, Fukui A, Akiyoshi S, Hayashi YK, Ishii E, Nishino I.
    Source:
      Neuromuscul Disord. 23(11):917-21. 2013.
    PMID:
      24011703
  15. Author(s):
      Murakami N, Hayashi YK, Oto Y, Shiraishi M, Itabashi H, Kudo K, Nishino I, Nonaka I, Nagai T.
    Source:
      Neuromuscul Disord. 23(5):441-4. 2013.
    PMID:
      23489663
  16. Author(s):
      Ravenscroft G, Miyatake S, Lehtokari VL, Todd EJ, Vornanen P, Yau KS, Hayashi YK, Miyake N, Tsurusaki Y, et al.
    Source:
      Am J Hum Genet. 93(1):6-18. 2013.
    PMID:
      23746549
  17. Author(s):
      Saitsu H, Nishimura T, Muramatsu K, Kodera H, Kumada S, Sugai K, Kasai-Yoshida E, Sawaura N, Nishida H, et al.
    Source:
      Nat Genet. 45(4):445-9. 2013.
    PMID:
      23435086
  18. Author(s):
      Shibata H, Yamamoto K, Sun Z, Oka A, Inoko H, Arinami T, Inada T, Ujike H, Itokawa M, et al.
    Source:
      Psychiatr Genet. 23(3):117-23. 2013.
    PMID:
      23474461
  19. Juvenile autophagic vacuolar myopathy - a new entity or variant?
    Author(s):
      Stenzel W, Nishino I, von Moers A, Kadry MA, Glaeser D, Heppner FL, Goebel HH.
    Source:
      Neuropathol Appl Neurobiol. 39(4):449-53. 2013.
    PMID:
      23324055
  20. Author(s):
      Takeuchi F, Yonemoto N, Nakamura H, Shimizu R, Komaki H, Mori-Yoshimura M, Hayashi YK, Nishino I, Kawai M, et al.
    Source:
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  22. Replication in a Japanese population that a MIR30E gene variation is associated with schizophrenia
    Author(s):
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    Source:
      Schizophr Res. 150(2-3):596-7. 2013.
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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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      Brain Res. 1470:89-97. 2012.
    PMID:
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  2. Author(s):
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    Source:
      J Neurol Sci. 314(1-2):92-6. 2012.
    PMID:
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    Source:
      Neurogenetics. 13(2):115-24. 2012.
    PMID:
      22371254
  4. Author(s):
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    Source:
      J Psychiatr Res. 46(4):555-9. 2012.
    PMID:
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  5. Author(s):
      Hattori A, Komaki H, Kawatani M, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Hayashi YK, et al.
    Source:
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    PMID:
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  6. Author(s):
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    Source:
      Biol Psychol. 89(1):117-22. 2012.
    PMID:
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  7. Author(s):
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    Source:
      J Hum Genet. 57(1):73-7. 2012.
    PMID:
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  8. Author(s):
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    Source:
      Sci Rep. 2:634. 2012.
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    Source:
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    PMID:
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    Source:
      Case Rep Neurol. 4(2):120-5. 2012.
    PMID:
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  11. Author(s):
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    Source:
      Brain Dev. 34(10):877-80. 2012.
    PMID:
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  12. Author(s):
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    Source:
      J Neurol Sci. 318(1-2):163-7. 2012.
    PMID:
      22541254
  13. Author(s):
      Kondo E, Nishimura T, Kosho T, Inaba Y, Mitsuhashi S, Ishida T, Baba A, Koike K, Nishino I, et al.
    Source:
      Am J Med Genet A. 158A(4):772-8. 2012.
    PMID:
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  14. Author(s):
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    Source:
      J Neurol. 259(11):2329-34. 2012.
    PMID:
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  15. Myotonic dystrophy type 2 is rare in the Japanese population
    Author(s):
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    Source:
      J Hum Genet. 57(3):219-20. 2012.
    PMID:
      22258159
  16. Author(s):
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      PLoS One. 7(12):e52002. 2012.
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      23251671
  17. Author(s):
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      Clin Neurol Neurosurg. 114(6):678-83. 2012.
    PMID:
      22613877
  18. Author(s):
      Sakakibara T, Sukigara S, Otsuki T, Takahashi A, Kaneko Y, Kaido T, Saito Y, Sato N, Nakagawa E, et al.
    Source:
      J Neurol Sci. 323(1-2):128-33. 2012.
    PMID:
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  19. Author(s):
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    Source:
      J Neuropathol Exp Neurol. 71(8):741-9. 2012.
    PMID:
      22805777
  20. Author(s):
      Sangatsuda Y, Nakamura M, Tomiyasu A, Deguchi A, Toyota Y, Goto Y, Nishino I, Ueno S, Sano A.
    Source:
      Mitochondrion. 12(6):617-22. 2012.
    PMID:
      23063709
  21. Author(s):
      Sasayama D, Hattori K, Teraishi T, Hori H, Ota M, Yoshida S, Arima K, Higuchi T, Amano N, et al.
    Source:
      Schizophr Res. 139(1-3):201-6. 2012.
    PMID:
      22742979
  22. Author(s):
      Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Matsuo J, Kawamoto Y, Kinoshita Y, Amano N, et al.
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      J Neural Transm. 119(3):313-8. 2012.
    PMID:
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  23. Author(s):
      Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Matsuo J, Kawamoto Y, Kinoshita Y, Hashikura M, et al.
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      J Affect Disord. 136(3):1047-52. 2012.
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      22169250
  24. Author(s):
      Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Tatsumi M, Higuchi T, Amano N, Kunugi H.
    Source:
      Prog Neuropsychopharmacol Biol Psychiatry. 38(2):341-4. 2012.
    PMID:
      22609474
  25. Author(s):
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      Alzheimers Res Ther. 4(4):33. 2012.
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      22898310
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      Neuropathol Appl Neurobiol. 38(2):132-41. 2012.
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      Eur J Neurol. 19(3):501-9. 2012.
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      J Med Genet. 49(12):777-84. 2012.
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  29. Teaching NeuroImages: unilateral arm and contralateral leg amyotrophy in FSHD: unusual presentation
    Author(s):
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      Neurology. 79(5):e46. 2012.
    PMID:
      22851725
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      Ann Rheum Dis. 71(10):1646-50. 2012.
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      Sukigara S, Liang WC, Komaki H, Fukuda T, Miyamoto T, Saito T, Saito Y, Nakagawa E, Sugai K, et al.
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      Neuromuscul Disord. 22(2):162-5. 2012.
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      Brain Dev. 34(9):776-9. 2012.
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      22269148
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      Tsuburaya RS, Monma K, Oya Y, Nakayama T, Fukuda T, Sugie H, Hayashi YK, Nonaka I, Nishino I.
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      Neuromuscul Disord. 22(5):389-93. 2012.
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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
  1. Author(s):
      Fujii T, Uchiyama H, Yamamoto N, Hori H, Tatsumi M, Ishikawa M, Arima K, Higuchi T, Kunugi H.
    Source:
      J Psychiatr Res. 45(1):47-53. 2011.
    PMID:
      20684831
  2. Author(s):
      Fujii T, Yamamoto N, Hori H, Hattori K, Sasayama D, Teraishi T, Hashikura M, Tatsumi M, Okamoto N, et al.
    Source:
      J Hum Genet. 56(11):806-9. 2011.
    PMID:
      21938001
  3. Author(s):
      Kawashima H1, Ishii C, Yamanaka G, Ioi H, Nishimata S, Kashiwagi Y, Takekuma K, Miyajima T, Hoshika A, et al.
    Source:
      Pediatr Int. 53(2):159-61. 2011.
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      21501304
  4. Author(s):
      Komaki H, Hayashi YK, Tsuburaya R, Sugie K, Kato M, Nagai T, Imataka G, Suzuki S, Saitoh S, et al.
    Source:
      Neuromuscul Disord. 21(8):563-8. 2011.
    PMID:
      21632249
  5. Author(s):
      Mitsuhashi S, Hatakeyama H, Karahashi M, Koumura T, Nonaka I, Hayashi YK, Noguchi S, Sher RB, Nakagawa Y, et al.
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      Hum Mol. Genet. 20(19):3841-51. 2011.
    PMID:
      21750112
  6. Author(s):
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      Am J Hum Genet. 88(6):845-51. 2011.
    PMID:
      21665002
  7. Author(s):
      Ota M, Fujii T, Nemoto K, Tatsumi M, Moriguchi Y, Hashimoto R, Sato N, Iwata N, Kunugi H.
    Source:
      Prog Neuropsychopharmacol Biol Psychiatry. 35(8):1877-83. 2011.
    PMID:
      21839797
  8. Author(s):
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    Source:
      Cereb Cortex. 21(3):588-96. 2011.
    PMID:
      20624841
  9. Author(s):
      Saito Y, Komaki H, Hattori A, Takeuchi F, Sasaki M, Kawabata K, Mitsuhashi S, Tominaga K, Hayashi YK, et al.
    Source:
      Neuromuscul Disord. 21(7):489-93. 2011.
    PMID:
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  10. Author(s):
      Sasaki M, Matsufuji H, Inui T, Arima K.
    Source:
      Brain Dev. 33(5):390-3. 2011.
    PMID:
      20826074
  11. Author(s):
      Sasayama D, Hori H, Iijima Y, Teraishi T, Hattori K, Ota M, Fujii T, Higuchi T, Amano N, et al.
    Source:
      Behav Brain Funct. 7:23. 2011.
    PMID:
      21726461
  12. Author(s):
      Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Iijima Y, Tatsumi M, Higuchi T, Amano N, et al.
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      Behav Brain Funct. 7:35. 2011.
    PMID:
      21843369
  13. Author(s):
      Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Matsuo J, Kawamoto Y, Kinoshita Y, Hashikura M, et al.
    Source:
      J Affect Disord. 132(3):319-24. 2011.
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      J Hum Genet. 56(8):613-6. 2011.
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    PMID:
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      Takeshita E, Saito Y, Nakagawa E, Komaki H, Sugai K, Sasaki M, Nezu A, Kitamura J, Itoh M, et al.
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      J Neurol Sci. 308(1-2):168-72. 2011.
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  20. Lobulated fibers in a patient with 46-year history of limb-girdle muscle weakness
    Author(s):
      Tsuburaya R, Suzuki T, Saiki K, Nonaka I, Sugita H, Hayashi YK, Nishino I.
    Source:
      Neuropathology. 31(4):455-7. 2011.
    PMID:
      21518015
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      Waga C, Okamoto N, Ondo Y, Fukumura-Kato R, Goto Y, Kohsaka S, Uchino S.
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    PMID:
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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
  1. Author(s):
      Amagane H, Watanabe Y, Kaneko N, Nunokawa A, Muratake T, Ishiguro H, Arinami T, Ujike H, Inada T, et al.
    Source:
      Schizophr Res. 118(1-3):106-12. 2010.
    PMID:
      20188514
  2. Author(s):
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      Seizure. 19(5):274-9. 2010.
    PMID:
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      World J Biol Psychiatry. 11(2 Pt 2):431-8. 2010.
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      J Hum Genet. 55(9):590-9. 2010.
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      20613765
  5. Author(s):
      Kim H, Cho A, Lim BC, Kim MJ, Kim KJ, Nishino I, Hwang YS, Chae JH.
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      Muscle Nerve. 41(6):879-82. 2010.
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      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:
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  7. Author(s):
      Mitsuhashi H, Hayashi YK, Matsuda C, Noguchi S, Wakatsuki S, Araki T, Nishino I.
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      J Cell Sci. 123(Pt 22):3893-900. 2010.
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  8. Author(s):
      Osaka H, Hamanoue H, Yamamoto R, Nezu A, Sasaki M, Saitsu H, Kurosawa K, Shimbo H, Matsumoto N, et al.
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      Ann Neurol. 68(2):250-4. 2010.
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      Prog Neuropsychopharmacol Biol Psychiatry. 34(2):401-5. 2010.
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    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.
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      Acta Neuropathol. 119(4):481-6. 2010.
    PMID:
      20179953

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