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Naoki Suzuki, M.D.,Ph.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Inoue-Shibui A, Niihori T, Kobayashi M, Suzuki N, Izumi R, Warita H, Hara K, Shirota M, Funayama R, Nakayama K, Nishino I, Aoki M, Aoki Y. A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy. J Hum Genet. 2021 Mar 20. PMID: 33744911.
    Citations:    Fields:    
  2. Amato AA, Hanna MG, Machado PM, Badrising UA, Chinoy H, Benveniste O, Karanam AK, Wu M, Tankó LB, Schubert-Tennigkeit AA, Papanicolaou DA, Lloyd TE, Needham M, Liang C, Reardon KA, de Visser M, Ascherman DP, Barohn RJ, Dimachkie MM, Miller JAL, Kissel JT, Oskarsson B, Joyce NC, Van den Bergh P, Baets J, De Bleecker JL, Karam C, David WS, Mirabella M, Nations SP, Jung HH, Pegoraro E, Maggi L, Rodolico C, Filosto M, Shaibani AI, Sivakumar K, Goyal NA, Mori-Yoshimura M, Yamashita S, Suzuki N, Aoki M, Katsuno M, Morihata H, Murata K, Nodera H, Nishino I, Romano CD, Williams VSL, Vissing J, Zhang Auberson L. Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT. Neurology. 2021 Mar 23; 96(12):e1595-e1607. PMID: 33597289.
    Citations: 1     Fields:    
  3. Osana S, Kitajima Y, Suzuki N, Nunomiya A, Takada H, Kubota T, Murayama K, Nagatomi R. Puromycin-sensitive aminopeptidase is required for C2C12 myoblast proliferation and differentiation. J Cell Physiol. 2021 Jul; 236(7):5293-5305. PMID: 33378552.
    Citations:    Fields:    
  4. Oikawa Y, Izumi R, Koide M, Hagiwara Y, Kanzaki M, Suzuki N, Kikuchi K, Matsuhashi T, Akiyama Y, Ichijo M, Watanabe S, Toyohara T, Suzuki T, Mishima E, Akiyama Y, Ogata Y, Suzuki C, Hayashi H, Kodama EN, Hayashi KI, Itoi E, Aoki M, Kure S, Abe T. Mitochondrial dysfunction underlying sporadic inclusion body myositis is ameliorated by the mitochondrial homing drug MA-5. PLoS One. 2020; 15(12):e0231064. PMID: 33264289.
    Citations:    Fields:    Translation:HumansCells
  5. Osana S, Kitajima Y, Suzuki N, Xu Y, Murayama K, Nagatomi R. siRNA knockdown of alanine aminopeptidase impairs myoblast proliferation and differentiation. Exp Cell Res. 2020 12 01; 397(1):112337. PMID: 33091420.
    Citations:    Fields:    
  6. Suzuki N, Soga T, Izumi R, Toyoshima M, Shibasaki M, Sato I, Kudo Y, Aoki M, Kato M. Hybrid Assistive Limb® for sporadic inclusion body myositis: A case series. J Clin Neurosci. 2020 Nov; 81:92-94. PMID: 33222978.
    Citations:    Fields:    Translation:Humans
  7. Nakamura R, Misawa K, Tohnai G, Nakatochi M, Furuhashi S, Atsuta N, Hayashi N, Yokoi D, Watanabe H, Watanabe H, Katsuno M, Izumi Y, Kanai K, Hattori N, Morita M, Taniguchi A, Kano O, Oda M, Shibuya K, Kuwabara S, Suzuki N, Aoki M, Ohta Y, Yamashita T, Abe K, Hashimoto R, Aiba I, Okamoto K, Mizoguchi K, Hasegawa K, Okada Y, Ishihara T, Onodera O, Nakashima K, Kaji R, Kamatani Y, Ikegawa S, Momozawa Y, Kubo M, Ishida N, Minegishi N, Nagasaki M, Sobue G. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. Commun Biol. 2020 Sep 23; 3(1):526. PMID: 32968195.
    Citations: 2     
  8. Kitajima Y, Yoshioka K, Suzuki N. The ubiquitin-proteasome system in regulation of the skeletal muscle homeostasis and atrophy: from basic science to disorders. J Physiol Sci. 2020 Sep 16; 70(1):40. PMID: 32938372.
    Citations: 2     Fields:    
  9. Kitajima Y, Suzuki N, Yoshioka K, Izumi R, Tateyama M, Tashiro Y, Takahashi R, Aoki M, Ono Y. Inducible Rpt3, a Proteasome Component, Knockout in Adult Skeletal Muscle Results in Muscle Atrophy. Front Cell Dev Biol. 2020; 8:859. PMID: 32984340.
    Citations:    
  10. Watanabe Y, Nakagawa T, Akiyama T, Nakagawa M, Suzuki N, Warita H, Aoki M, Nakayama K. An Amyotrophic Lateral Sclerosis-Associated Mutant of C21ORF2 Is Stabilized by NEK1-Mediated Hyperphosphorylation and the Inability to Bind FBXO3. iScience. 2020 Aug 21; 23(9):101491. PMID: 32891887.
    Citations: 1     
  11. Ishigaki S, Riku Y, Fujioka Y, Endo K, Iwade N, Kawai K, Ishibashi M, Yokoi S, Katsuno M, Watanabe H, Mori K, Akagi A, Yokota O, Terada S, Kawakami I, Suzuki N, Warita H, Aoki M, Yoshida M, Sobue G. Aberrant interaction between FUS and SFPQ in neurons in a wide range of FTLD spectrum diseases. Brain. 2020 08 01; 143(8):2398-2405. PMID: 32770214.
    Citations: 3     Fields:    Translation:HumansCells
  12. Izumi R, Takahashi T, Suzuki N, Niihori T, Ono H, Nakamura N, Katada S, Kato M, Warita H, Tateyama M, Aoki Y, Aoki M. The genetic profile of dysferlinopathy in a cohort of 209 cases: Genotype-phenotype relationship and a hotspot on the inner DysF domain. Hum Mutat. 2020 Sep; 41(9):1540-1554. PMID: 32400077.
    Citations: 2     Fields:    
  13. Leventoux N, Morimoto S, Hara K, Nakamura S, Ozawa F, Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Warita H, Aoki M, Okano H. Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation. Stem Cell Res. 2020 Jun 28; 47:101896. PMID: 32659732.
    Citations:    Fields:    
  14. Samukawa M, Nakamura N, Hirano M, Morikawa M, Sakata H, Nishino I, Izumi R, Suzuki N, Kuroda H, Shiga K, Saigoh K, Aoki M, Kusunoki S. Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review. Eur Neurol. 2020; 83(3):317-322. PMID: 32564019.
    Citations:    Fields:    Translation:Humans
  15. Suzuki N, Akiyama T, Warita H, Aoki M. Omics Approach to Axonal Dysfunction of Motor Neurons in Amyotrophic Lateral Sclerosis (ALS). Front Neurosci. 2020; 14:194. PMID: 32269505.
    Citations: 3     
  16. Ono H, Suzuki N, Kanno SI, Kawahara G, Izumi R, Takahashi T, Kitajima Y, Osana S, Nakamura N, Akiyama T, Ikeda K, Shijo T, Mitsuzawa S, Nagatomi R, Araki N, Yasui A, Warita H, Hayashi YK, Miyake K, Aoki M. AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy. Mol Ther. 2020 04 08; 28(4):1133-1153. PMID: 32087766.
    Citations: 1     Fields:    
  17. Hayashi N, Atsuta N, Yokoi D, Nakamura R, Nakatochi M, Katsuno M, Izumi Y, Kanai K, Hattori N, Taniguchi A, Morita M, Kano O, Shibuya K, Kuwabara S, Suzuki N, Aoki M, Aiba I, Mizoguchi K, Oda M, Kaji R, Sobue G. Prognosis of amyotrophic lateral sclerosis patients undergoing tracheostomy invasive ventilation therapy in Japan. J Neurol Neurosurg Psychiatry. 2020 03; 91(3):285-290. PMID: 31937581.
    Citations: 1     Fields:    Translation:Humans
  18. Mori-Yoshimura M, Yamashita S, Suzuki N, Katsuno M, Murata K, Nodera H, Teshima R, Inamura T, Nishino I, Aoki M. [Late phase II/III study of BYM338 in patients with sporadic inclusion body myositis (RESILIENT): Japanese cohort data]. Rinsho Shinkeigaku. 2019 Dec 25; 59(12):806-813. PMID: 31761834.
    Citations:    Fields:    Translation:HumansCTClinical Trials
  19. Suzuki N, Nishiyama A, Kato M, Warita H, Aoki M. [Familial Amyotrophic Lateral Sclerosis]. Brain Nerve. 2019 Nov; 71(11):1169-1181. PMID: 31722303.
    Citations: 2     Fields:    Translation:HumansAnimalsCells
  20. Aoki M, Warita H, Kato M, Suzuki N. [Application of Hepatocyte Growth Factor for Amyotrophic Lateral Sclerosis]. Brain Nerve. 2019 Nov; 71(11):1253-1260. PMID: 31722311.
    Citations:    Fields:    Translation:HumansAnimalsCells
  21. Yu Y, Nakagawa T, Morohoshi A, Nakagawa M, Ishida N, Suzuki N, Aoki M, Nakayama K. Pathogenic mutations in the ALS gene CCNF cause cytoplasmic mislocalization of Cyclin F and elevated VCP ATPase activity. Hum Mol Genet. 2019 10 15; 28(20):3486-3497. PMID: 31577344.
    Citations: 6     Fields:    Translation:AnimalsCells
  22. Nakamura N, Izumi R, Hoshi Y, Takai Y, Ono R, Suzuki N, Nagai T, Ishii Y, Ishii T, Harigae H, Okada S, Aiba S, Okiyama N, Fujimoto M, Kuroda H, Tateyama M, Aoki M. FDG-PET detects extensive calcinosis cutis in anti-NXP2 antibody-positive dermatomyositis. Rheumatology (Oxford). 2019 10 01; 58(10):1888. PMID: 30879053.
    Citations:    Fields:    Translation:Humans
  23. Hanna MG, Badrising UA, Benveniste O, Lloyd TE, Needham M, Chinoy H, Aoki M, Machado PM, Liang C, Reardon KA, de Visser M, Ascherman DP, Barohn RJ, Dimachkie MM, Miller JAL, Kissel JT, Oskarsson B, Joyce NC, Van den Bergh P, Baets J, De Bleecker JL, Karam C, David WS, Mirabella M, Nations SP, Jung HH, Pegoraro E, Maggi L, Rodolico C, Filosto M, Shaibani AI, Sivakumar K, Goyal NA, Mori-Yoshimura M, Yamashita S, Suzuki N, Katsuno M, Murata K, Nodera H, Nishino I, Romano CD, Williams VSL, Vissing J, Auberson LZ, Wu M, de Vera A, Papanicolaou DA, Amato AA. Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial. Lancet Neurol. 2019 09; 18(9):834-844. PMID: 31397289.
    Citations: 11     Fields:    Translation:HumansCTClinical Trials
  24. Chen W, Nyasha MR, Koide M, Tsuchiya M, Suzuki N, Hagiwara Y, Aoki M, Kanzaki M. In vitro exercise model using contractile human and mouse hybrid myotubes. Sci Rep. 2019 08 15; 9(1):11914. PMID: 31417107.
    Citations: 4     Fields:    Translation:HumansAnimalsCells
  25. Akiyama T, Suzuki N, Ishikawa M, Fujimori K, Sone T, Kawada J, Funayama R, Fujishima F, Mitsuzawa S, Ikeda K, Ono H, Shijo T, Osana S, Shirota M, Nakagawa T, Kitajima Y, Nishiyama A, Izumi R, Morimoto S, Okada Y, Kamei T, Nishida M, Nogami M, Kaneda S, Ikeuchi Y, Mitsuhashi H, Nakayama K, Fujii T, Warita H, Okano H, Aoki M. Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons. EBioMedicine. 2019 Jul; 45:362-378. PMID: 31262712.
    Citations: 7     Fields:    Translation:HumansAnimalsCells
  26. Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata KY, Mori M, Inamori Y, Matsui N, Kimura E, Kusaka H, Kondo T, Ito H, Higuchi I, Hashiguchi A, Nodera H, Kaji R, Tateyama M, Izumi R, Ono H, Kato M, Warita H, Takahashi T, Nishino I, Aoki M. The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan. Orphanet J Rare Dis. 2019 06 26; 14(1):155. PMID: 31242950.
    Citations: 1     Fields:    Translation:Humans
  27. Takeda T, Iijima M, Shimizu Y, Yoshizawa H, Miyashiro M, Onizuka H, Yamamoto T, Nishiyama A, Suzuki N, Aoki M, Shibata N, Kitagawa K. p.N345K mutation in TARDBP in a patient with familial amyotrophic lateral sclerosis: An autopsy case. Neuropathology. 2019 Aug; 39(4):286-293. PMID: 31124595.
    Citations:    Fields:    Translation:HumansCells
  28. Inoue-Shibui A, Kato M, Suzuki N, Kobayashi J, Takai Y, Izumi R, Kawauchi Y, Kuroda H, Warita H, Aoki M. Interstitial pneumonia and other adverse events in riluzole-administered amyotrophic lateral sclerosis patients: a retrospective observational study. BMC Neurol. 2019 Apr 27; 19(1):72. PMID: 31029113.
    Citations: 1     Fields:    Translation:Humans
  29. Eura N, Sugie K, Suzuki N, Kiriyama T, Izumi T, Shimakura N, Kato M, Aoki M. A juvenile sporadic amyotrophic lateral sclerosis case with P525L mutation in the FUS gene: A rare co-occurrence of autism spectrum disorder and tremor. J Neurol Sci. 2019 Mar 15; 398:67-68. PMID: 30684766.
    Citations: 3     Fields:    Translation:Humans
  30. Miyabayashi T, Ochiai T, Suzuki N, Aoki M, Inui T, Okubo Y, Sato R, Togashi N, Takashima H, Ishiura H, Tsuji S, Koh K, Takiyama Y, Haginoya K. A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy. J Hum Genet. 2019 Feb; 64(2):171-176. PMID: 30467354.
    Citations: 1     Fields:    Translation:Humans
  31. Kitajima Y, Suzuki N, Nunomiya A, Osana S, Yoshioka K, Tashiro Y, Takahashi R, Ono Y, Aoki M, Nagatomi R. The Ubiquitin-Proteasome System Is Indispensable for the Maintenance of Muscle Stem Cells. Stem Cell Reports. 2018 12 11; 11(6):1523-1538. PMID: 30416048.
    Citations: 13     Fields:    Translation:AnimalsCells
  32. Kawaguchi N, Izumi R, Kobayashi M, Tateyama M, Suzuki N, Fujishima F, Fujimori J, Aoki M, Nakashima I. Extranodal NK/T-cell Lymphoma Mimicking Granulomatous Myositis. Intern Med. 2019 Jan 15; 58(2):277-282. PMID: 30146568.
    Citations: 1     Fields:    Translation:Humans
  33. Shijo T, Warita H, Suzuki N, Ikeda K, Mitsuzawa S, Akiyama T, Ono H, Nishiyama A, Izumi R, Kitajima Y, Aoki M. Antagonizing bone morphogenetic protein 4 attenuates disease progression in a rat model of amyotrophic lateral sclerosis. Exp Neurol. 2018 09; 307:164-179. PMID: 29932880.
    Citations: 3     Fields:    Translation:HumansAnimals
  34. Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Kato M, Warita H, Izumi R, Osana S, Koyama S, Kato T, Suzuki Y, Aoki M. TARDBP p.G376D mutation, found in rapid progressive familial ALS, induces mislocalization of TDP-43. eNeurologicalSci. 2018 Jun; 11:20-22. PMID: 29928714.
    Citations: 1     
  35. Shibata S, Izumi R, Hara T, Ohshima R, Nakamura N, Suzuki N, Kato K, Katori Y, Tateyama M, Kuroda H, Aoki M. Five-year history of dysphagia as a sole initial symptom in inclusion body myositis. J Neurol Sci. 2017 10 15; 381:325-327. PMID: 28991709.
    Citations: 3     Fields:    Translation:Humans
  36. Shijo T, Warita H, Suzuki N, Kitajima Y, Ikeda K, Akiyama T, Ono H, Mitsuzawa S, Nishiyama A, Izumi R, Aoki M. Aberrant astrocytic expression of chondroitin sulfate proteoglycan receptors in a rat model of amyotrophic lateral sclerosis. J Neurosci Res. 2018 02; 96(2):222-233. PMID: 28752900.
    Citations: 2     Fields:    Translation:HumansAnimalsCells
  37. Tawara N, Yamashita S, Zhang X, Korogi M, Zhang Z, Doki T, Matsuo Y, Nakane S, Maeda Y, Sugie K, Suzuki N, Aoki M, Ando Y. Pathomechanisms of anti-cytosolic 5'-nucleotidase 1A autoantibodies in sporadic inclusion body myositis. Ann Neurol. 2017 Apr; 81(4):512-525. PMID: 28318044.
    Citations: 9     Fields:    Translation:HumansAnimalsCells
  38. Nishiyama A, Niihori T, Warita H, Izumi R, Akiyama T, Kato M, Suzuki N, Aoki Y, Aoki M. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. Neurobiol Aging. 2017 05; 53:194.e1-194.e8. PMID: 28160950.
    Citations: 11     Fields:    Translation:Humans
  39. Suzuki N, Izumi R, Kato M, Warita H, Aoki M. [Therapeutic development for GNE myopathy.] Clin Calcium. 2017; 27(3):429-434. PMID: 28232658.
    Citations:    Fields:    Translation:Humans
  40. Suwa Y, Suzuki N, Soga T, Harada R, Shibui A, Kuroda H, Izumi R, Tateyama M, Nakashima I, Sonoo M, Aoki M. Sporadic Inclusion Body Myositis Manifesting as Isolated Muscle Weakness of the Finger Flexors Three Years after Disease Onset. Intern Med. 2016; 55(23):3521-3524. PMID: 27904121.
    Citations: 1     Fields:    Translation:Humans
  41. Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata KY, Inamori Y, Matsui N, Kimura E, Kusaka H, Kondo T, Higuchi I, Kaji R, Tateyama M, Izumi R, Ono H, Kato M, Warita H, Takahashi T, Nishino I, Aoki M. Multicenter questionnaire survey for sporadic inclusion body myositis in Japan. Orphanet J Rare Dis. 2016 11 08; 11(1):146. PMID: 27821140.
    Citations: 2     Fields:    Translation:Humans
  42. Tian F, Yang W, Mordes DA, Wang JY, Salameh JS, Mok J, Chew J, Sharma A, Leno-Duran E, Suzuki-Uematsu S, Suzuki N, Han SS, Lu FK, Ji M, Zhang R, Liu Y, Strominger J, Shneider NA, Petrucelli L, Xie XS, Eggan K. Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging. Nat Commun. 2016 10 31; 7:13283. PMID: 27796305.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  43. Nishiyama A, Warita H, Takahashi T, Suzuki N, Nishiyama S, Tano O, Akiyama T, Watanabe Y, Takahashi K, Kuroda H, Kato M, Tateyama M, Niihori T, Aoki Y, Aoki M. Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutation. Clin Neurol Neurosurg. 2016 Nov; 150:194-196. PMID: 27543311.
    Citations:    Fields:    Translation:Humans
  44. Burberry A, Suzuki N, Wang JY, Moccia R, Mordes DA, Stewart MH, Suzuki-Uematsu S, Ghosh S, Singh A, Merkle FT, Koszka K, Li QZ, Zon L, Rossi DJ, Trowbridge JJ, Notarangelo LD, Eggan K. Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease. Sci Transl Med. 2016 07 13; 8(347):347ra93. PMID: 27412785.
    Citations: 73     Fields:    Translation:Animals
  45. Aizawa H, Hideyama T, Yamashita T, Kimura T, Suzuki N, Aoki M, Kwak S. Deficient RNA-editing enzyme ADAR2 in an amyotrophic lateral sclerosis patient with a FUS(P525L) mutation. J Clin Neurosci. 2016 Oct; 32:128-9. PMID: 27343041.
    Citations: 9     Fields:    Translation:HumansCells
  46. Richards WD, Tsujimura T, Miara LJ, Wang Y, Kim JC, Ong SP, Uechi I, Suzuki N, Ceder G. Design and synthesis of the superionic conductor Na10SnP2S12. Nat Commun. 2016 Mar 17; 7:11009. PMID: 26984102.
    Citations: 10     Fields:    
  47. Ichiyanagi N, Fujimori K, Yano M, Ishihara-Fujisaki C, Sone T, Akiyama T, Okada Y, Akamatsu W, Matsumoto T, Ishikawa M, Nishimoto Y, Ishihara Y, Sakuma T, Yamamoto T, Tsuiji H, Suzuki N, Warita H, Aoki M, Okano H. Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells. Stem Cell Reports. 2016 Apr 12; 6(4):496-510. PMID: 26997647.
    Citations: 26     Fields:    Translation:HumansCells
  48. Intoh A, Suzuki N, Koszka K, Eggan K. SLC52A3, A Brown-Vialetto-van Laere syndrome candidate gene is essential for mouse development, but dispensable for motor neuron differentiation. Hum Mol Genet. 2016 05 01; 25(9):1814-23. PMID: 26976849.
    Citations: 7     Fields:    Translation:HumansAnimalsCells
  49. Akiyama T, Warita H, Kato M, Nishiyama A, Izumi R, Ikeda C, Kamada M, Suzuki N, Aoki M. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan. Muscle Nerve. 2016 09; 54(3):398-404. PMID: 26823199.
    Citations: 5     Fields:    Translation:Humans
  50. Sasaki A, Sato N, Suzuki N, Kano M, Tanaka Y, Kanazawa M, Aoki M, Fukudo S. Associations between Single-Nucleotide Polymorphisms in Corticotropin-Releasing Hormone-Related Genes and Irritable Bowel Syndrome. PLoS One. 2016; 11(2):e0149322. PMID: 26882083.
    Citations: 5     Fields:    Translation:Humans
  51. Komuro H, Sato N, Sasaki A, Suzuki N, Kano M, Tanaka Y, Yamaguchi-Kabata Y, Kanazawa M, Warita H, Aoki M, Fukudo S. Corticotropin-Releasing Hormone Receptor 2 Gene Variants in Irritable Bowel Syndrome. PLoS One. 2016; 11(1):e0147817. PMID: 26808377.
    Citations: 5     Fields:    Translation:Humans
  52. Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, Agnello M, Agostinis P, Aguilar PV, Aguirre-Ghiso J, Airoldi EM, Ait-Si-Ali S, Akematsu T, Akporiaye ET, Al-Rubeai M, Albaiceta GM, Albanese C, Albani D, Albert ML, Aldudo J, Algül H, Alirezaei M, Alloza I, Almasan A, Almonte-Beceril M, Alnemri ES, Alonso C, Altan-Bonnet N, Altieri DC, Alvarez S, Alvarez-Erviti L, Alves S, Amadoro G, Amano A, Amantini C, Ambrosio S, Amelio I, Amer AO, Amessou M, Amon A, An Z, Anania FA, Andersen SU, Andley UP, Andreadi CK, Andrieu-Abadie N, Anel A, Ann DK, Anoopkumar-Dukie S, Antonioli M, Aoki H, Apostolova N, Aquila S, Aquilano K, Araki K, Arama E, Aranda A, Araya J, Arcaro A, Arias E, Arimoto H, Ariosa AR, Armstrong JL, Arnould T, Arsov I, Asanuma K, Askanas V, Asselin E, Atarashi R, Atherton SS, Atkin JD, Attardi LD, Auberger P, Auburger G, Aurelian L, Autelli R, Avagliano L, Avantaggiati ML, Avrahami L, Awale S, Azad N, Bachetti T, Backer JM, Bae DH, Bae JS, Bae ON, Bae SH, Baehrecke EH, Baek SH, Baghdiguian S, Bagniewska-Zadworna A, Bai H, Bai J, Bai XY, Bailly Y, Balaji KN, Balduini W, Ballabio A, Balzan R, Banerjee R, Bánhegyi G, Bao H, Barbeau B, Barrachina MD, Barreiro E, Bartel B, Bartolomé A, Bassham DC, Bassi MT, Bast RC, Basu A, Batista MT, Batoko H, Battino M, Bauckman K, Baumgarner BL, Bayer KU, Beale R, Beaulieu JF, Beck GR, Becker C, Beckham JD, Bédard PA, Bednarski PJ, Begley TJ, Behl C, Behrends C, Behrens GM, Behrns KE, Bejarano E, Belaid A, Belleudi F, Bénard G, Berchem G, Bergamaschi D, Bergami M, Berkhout B, Berliocchi L, Bernard A, Bernard M, Bernassola F, Bertolotti A, Bess AS, Besteiro S, Bettuzzi S, Bhalla S, Bhattacharyya S, Bhutia SK, Biagosch C, Bianchi MW, Biard-Piechaczyk M, Billes V, Bincoletto C, Bingol B, Bird SW, Bitoun M, Bjedov I, Blackstone C, Blanc L, Blanco GA, Blomhoff HK, Boada-Romero E, Böckler S, Boes M, Boesze-Battaglia K, Boise LH, Bolino A, Boman A, Bonaldo P, Bordi M, Bosch J, Botana LM, Botti J, Bou G, Bouché M, Bouchecareilh M, Boucher MJ, Boulton ME, Bouret SG, Boya P, Boyer-Guittaut M, Bozhkov PV, Brady N, Braga VM, Brancolini C, Braus GH, Bravo-San Pedro JM, Brennan LA, Bresnick EH, Brest P, Bridges D, Bringer MA, Brini M, Brito GC, Brodin B, Brookes PS, Brown EJ, Brown K, Broxmeyer HE, Bruhat A, Brum PC, Brumell JH, Brunetti-Pierri N, Bryson-Richardson RJ, Buch S, Buchan AM, Budak H, Bulavin DV, Bultman SJ, Bultynck G, Bumbasirevic V, Burelle Y, Burke RE, Burmeister M, Bütikofer P, Caberlotto L, Cadwell K, Cahova M, Cai D, Cai J, Cai Q, Calatayud S, Camougrand N, Campanella M, Campbell GR, Campbell M, Campello S, Candau R, Caniggia I, Cantoni L, Cao L, Caplan AB, Caraglia M, Cardinali C, Cardoso SM, Carew JS, Carleton LA, Carlin CR, Carloni S, Carlsson SR, Carmona-Gutierrez D, Carneiro LA, Carnevali O, Carra S, Carrier A, Carroll B, Casas C, Casas J, Cassinelli G, Castets P, Castro-Obregon S, Cavallini G, Ceccherini I, Cecconi F, Cederbaum AI, Ceña V, Cenci S, Cerella C, Cervia D, Cetrullo S, Chaachouay H, Chae HJ, Chagin AS, Chai CY, Chakrabarti G, Chamilos G, Chan EY, Chan MT, Chandra D, Chandra P, Chang CP, Chang RC, Chang TY, Chatham JC, Chatterjee S, Chauhan S, Che Y, Cheetham ME, Cheluvappa R, Chen CJ, Chen G, Chen GC, Chen G, Chen H, Chen JW, Chen JK, Chen M, Chen M, Chen P, Chen Q, Chen Q, Chen SD, Chen S, Chen SS, Chen W, Chen WJ, Chen WQ, Chen W, Chen X, Chen YH, Chen YG, Chen Y, Chen Y, Chen Y, Chen YJ, Chen YQ, Chen Y, Chen Z, Chen Z, Cheng A, Cheng CH, Cheng H, Cheong H, Cherry S, Chesney J, Cheung CH, Chevet E, Chi HC, Chi SG, Chiacchiera F, Chiang HL, Chiarelli R, Chiariello M, Chieppa M, Chin LS, Chiong M, Chiu GN, Cho DH, Cho SG, Cho WC, Cho YY, Cho YS, Choi AM, Choi EJ, Choi EK, Choi J, Choi ME, Choi SI, Chou TF, Chouaib S, Choubey D, Choubey V, Chow KC, Chowdhury K, Chu CT, Chuang TH, Chun T, Chung H, Chung T, Chung YL, Chwae YJ, Cianfanelli V, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 2016; 12(1):1-222. PMID: 26799652.
    Citations: 1890     Fields:    Translation:HumansAnimals
  53. Izumi R, Niihori T, Takahashi T, Suzuki N, Tateyama M, Watanabe C, Sugie K, Nakanishi H, Sobue G, Kato M, Warita H, Aoki Y, Aoki M. Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing. Neurol Genet. 2015 Dec; 1(4):e36. PMID: 27066573.
    Citations: 3     
  54. Suzuki N, Aoki M, Warita H, Kato M, Mizuno H, Shimakura N, Akiyama T, Furuya H, Hokonohara T, Iwaki A, Togashi S, Konno H, Itoyama Y. FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion. J Hum Genet. 2015 Oct; 60(10):653-4. PMID: 26500017.
    Citations:    Fields:    
  55. Izumi R, Warita H, Niihori T, Takahashi T, Tateyama M, Suzuki N, Nishiyama A, Shirota M, Funayama R, Nakayama K, Mitsuhashi S, Nishino I, Aoki Y, Aoki M. Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutation. Neurol Genet. 2015 Oct; 1(3):e23. PMID: 27066560.
    Citations: 6     
  56. Kitajima Y, Tashiro Y, Suzuki N, Warita H, Kato M, Tateyama M, Ando R, Izumi R, Yamazaki M, Abe M, Sakimura K, Ito H, Urushitani M, Nagatomi R, Takahashi R, Aoki M. Proteasome dysfunction induces muscle growth defects and protein aggregation. J Cell Sci. 2014 Dec 15; 127(Pt 24):5204-17. PMID: 25380823.
    Citations: 15     Fields:    Translation:AnimalsCells
  57. Izumi R, Niihori T, Suzuki N, Sasahara Y, Rikiishi T, Nishiyama A, Nishiyama S, Endo K, Kato M, Warita H, Konno H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Nakayama K, Kure S, Matsubara Y, Aoki Y, Aoki M. GNE myopathy associated with congenital thrombocytopenia: a report of two siblings. Neuromuscul Disord. 2014 Dec; 24(12):1068-72. PMID: 25257349.
    Citations: 12     Fields:    Translation:HumansCells
  58. de Boer AS, Koszka K, Kiskinis E, Suzuki N, Davis-Dusenbery BN, Eggan K. Genetic validation of a therapeutic target in a mouse model of ALS. Sci Transl Med. 2014 Aug 06; 6(248):248ra104. PMID: 25100738.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  59. Aoki M, Suzuki N. [Sporadic inclusion body myositis and amyloid]. Brain Nerve. 2014 Jul; 66(7):739-48. PMID: 24998819.
    Citations:    Fields:    Translation:Humans
  60. Akaishi T, Tateyama M, Kato K, Miura E, Izumi R, Endo K, Sugeno N, Suzuki N, Baba T, Misu T, Kikuchi A, Hasegawa T, Konosu-Fukaya S, Fujishima F, Suzuki H, Nakashima I, Aoki M. An autopsy case involving a 12-year history of amyotrophic lateral sclerosis with CIDP-like polyneuropathy. Intern Med. 2014; 53(12):1371-5. PMID: 24930660.
    Citations:    Fields:    Translation:Humans
  61. Aoki M, Suzuki N, Kato M, Warita H. [Recent progress in diagnosis and pathomechanism of inclusion body myositis]. Rinsho Shinkeigaku. 2014; 54(12):1115-8. PMID: 25672724.
    Citations:    Fields:    Translation:Humans
  62. Suzuki N, Maroof AM, Merkle FT, Koszka K, Intoh A, Armstrong I, Moccia R, Davis-Dusenbery BN, Eggan K. The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD. Nat Neurosci. 2013 Dec; 16(12):1725-7. PMID: 24185425.
    Citations: 38     Fields:    Translation:HumansAnimalsCells
  63. Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y. Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure. J Hum Genet. 2013 May; 58(5):259-66. PMID: 23446887.
    Citations: 12     Fields:    Translation:Humans
  64. Suzuki N, Hattori A, Ieiri S, Tomikawa M, Kenmotsu H, Hashizume M. Formulation of wire control mechanism for surgical robot to create virtual reality environment aimed at conducting surgery inside the body. Stud Health Technol Inform. 2013; 184:424-30. PMID: 23400196.
    Citations: 2     Fields:    Translation:Humans
  65. Takahashi T, Aoki M, Suzuki N, Tateyama M, Yaginuma C, Sato H, Hayasaka M, Sugawara H, Ito M, Abe-Kondo E, Shimakura N, Ibi T, Kuru S, Wakayama T, Sobue G, Fujii N, Saito T, Matsumura T, Funakawa I, Mukai E, Kawanami T, Morita M, Yamazaki M, Hasegawa T, Shimizu J, Tsuji S, Kuzuhara S, Tanaka H, Yoshioka M, Konno H, Onodera H, Itoyama Y. Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B. J Neurol Neurosurg Psychiatry. 2013 Apr; 84(4):433-40. PMID: 23243261.
    Citations: 16     Fields:    Translation:Humans
  66. Kawaguchi N, Suzuki N, Tateyama M, Takai Y, Misu T, Nakashima I, Itoyama Y, Aoki M. Two cases of elderly-onset hereditary neuropathy with liability to pressure palsy manifesting bilateral peroneal nerve palsies. Case Rep Neurol. 2012 Sep; 4(3):149-55. PMID: 23185166.
    Citations: 3     
  67. Gallagher A, Tanaka N, Suzuki N, Liu H, Thiele EA, Stufflebeam SM. Diffuse cerebral language representation in tuberous sclerosis complex. Epilepsy Res. 2013 Mar; 104(1-2):125-33. PMID: 23092910.
    Citations: 2     Fields:    Translation:Humans
  68. Sato N, Suzuki N, Sasaki A, Aizawa E, Obayashi T, Kanazawa M, Mizuno T, Kano M, Aoki M, Fukudo S. Corticotropin-releasing hormone receptor 1 gene variants in irritable bowel syndrome. PLoS One. 2012; 7(9):e42450. PMID: 22957021.
    Citations: 12     Fields:    Translation:Humans
  69. Suzuki N, Kato S, Kato M, Warita H, Mizuno H, Kato M, Shimakura N, Akiyama H, Kobayashi Z, Konno H, Aoki M. FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation. J Neuropathol Exp Neurol. 2012 Sep; 71(9):779-88. PMID: 22878663.
    Citations: 11     Fields:    Translation:HumansCells
  70. Gallagher A, Tanaka N, Suzuki N, Liu H, Thiele EA, Stufflebeam SM. Decreased language laterality in tuberous sclerosis complex: a relationship between language dominance and tuber location as well as history of epilepsy. Epilepsy Behav. 2012 Sep; 25(1):36-41. PMID: 22980079.
    Citations: 4     Fields:    Translation:Humans
  71. Hara M, Minami M, Kamei S, Suzuki N, Kato M, Aoki M. Lower motor neuron disease caused by a novel FUS/TLS gene frameshift mutation. J Neurol. 2012 Oct; 259(10):2237-9. PMID: 22619056.
    Citations: 6     Fields:    Translation:HumansCells
  72. Nakata N, Suzuki N, Hattori A, Hirai N, Miyamoto Y, Fukuda K. Informatics in radiology: Intuitive user interface for 3D image manipulation using augmented reality and a smartphone as a remote control. Radiographics. 2012 Jul-Aug; 32(4):E169-74. PMID: 22556316.
    Citations: 1     Fields:    
  73. Aoki M, Suzuki N. [Sporadic inclusion body myositis in Japan]. Nihon Rinsho. 2012 May; 70(5):895-906. PMID: 22620019.
    Citations:    Fields:    Translation:Humans
  74. Mori-Yoshimura M, Monma K, Suzuki N, Aoki M, Kumamoto T, Tanaka K, Tomimitsu H, Nakano S, Sonoo M, Shimizu J, Sugie K, Nakamura H, Oya Y, Hayashi YK, Malicdan MC, Noguchi S, Murata M, Nishino I. Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations. J Neurol Sci. 2012 Jul 15; 318(1-2):100-5. PMID: 22507750.
    Citations: 19     Fields:    Translation:HumansCells
  75. Suzuki N, Takahashi T, Suzuki Y, Narikawa K, Kudo S, Suzuki H, Tateyama M, Aoki M. An autopsy case of a dysferlinopathy patient with cardiac involvement. Muscle Nerve. 2012 Feb; 45(2):298-9. PMID: 22246893.
    Citations: 1     Fields:    Translation:Humans
  76. Warita H, Kato M, Suzuki N, Itoyama Y, Aoki M. [Clinical translation of hepatocyte growth factor for amyotrophic lateral sclerosis]. Rinsho Shinkeigaku. 2012; 52(11):1214-7. PMID: 23196568.
    Citations:    Fields:    Translation:HumansAnimals
  77. Aoki M, Warita H, Suzuki N, Kato M. [Clinical genetics of amyotrophic lateral sclerosis in Japan: an update]. Rinsho Shinkeigaku. 2012; 52(11):844-7. PMID: 23196439.
    Citations:    Fields:    Translation:Humans
  78. Suzuki N, Hattori A. System development for unrestrictive view and 4D shape acquisition in abdominal cavity operation using virtual space. Stud Health Technol Inform. 2012; 173:506-11. PMID: 22357045.
    Citations:    Fields:    Translation:Humans
  79. Hattori A, Suzuki N, Ieiri S, Tomikawa M, Kenmotsu H, Hashizume M. Training system for NOTES and SPS surgery robot that enables spatiotemporal retrospective analysis of the training process. Stud Health Technol Inform. 2012; 173:166-70. PMID: 22356980.
    Citations:    Fields:    
  80. Suzuki N, Aoki M. [Amyotrophic lateral sclerosis (ALS) and fused in sarcoma/translocated in liposarcoma (FUS/TLS)]. Nihon Rinsho. 2011 Dec; 69 Suppl 10 Pt 2:389-93. PMID: 22755220.
    Citations:    Fields:    Translation:Humans
  81. Aoki M, Warita H, Suzuki N, Kato M, Itoyama Y. [Regenerative therapies for amyotrophic lateral sclerosis using hepatocyte growth factor]. Rinsho Shinkeigaku. 2011 Nov; 51(11):1195-8. PMID: 22277532.
    Citations:    Fields:    Translation:HumansAnimals
  82. Suzuki N, Tateyama M, Warita H, Izumi R, Nishino I, Aoki M. [Pathomechanism and prevalence of sporadic inclusion body myositis (sIBM)]. Rinsho Shinkeigaku. 2011 Nov; 51(11):964-6. PMID: 22277440.
    Citations:    Fields:    Translation:Humans
  83. Suzuki N, Aoki M. [Inclusion body myositis]. Brain Nerve. 2011 Nov; 63(11):1205-15. PMID: 22068473.
    Citations:    Fields:    Translation:HumansAnimalsCells
  84. Izumi R, Suzuki N, Nagata M, Hasegawa T, Abe Y, Saito Y, Mochizuki H, Tateyama M, Aoki M. A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure. Intern Med. 2011; 50(21):2663-8. PMID: 22041377.
    Citations: 7     Fields:    Translation:Humans
  85. Suzuki N, Akiyama T, Takahashi T, Komuro H, Warita H, Tateyama M, Itoyama Y, Aoki M. Continuous administration of poloxamer 188 reduces overload-induced muscular atrophy in dysferlin-deficient SJL mice. Neurosci Res. 2012 Feb; 72(2):181-6. PMID: 22044584.
    Citations: 9     Fields:    Translation:AnimalsCells
  86. Suzuki N, Aoki M, Mori-Yoshimura M, Hayashi YK, Nonaka I, Nishino I. Increase in number of sporadic inclusion body myositis (sIBM) in Japan. J Neurol. 2012 Mar; 259(3):554-6. PMID: 21800140.
    Citations: 11     Fields:    Translation:Humans
  87. Ito H, Fujita K, Nakamura M, Wate R, Kaneko S, Sasaki S, Yamane K, Suzuki N, Aoki M, Shibata N, Togashi S, Kawata A, Mochizuki Y, Mizutani T, Maruyama H, Hirano A, Takahashi R, Kawakami H, Kusaka H. Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease. Acta Neuropathol. 2011 Apr; 121(4):555-7. PMID: 21327942.
    Citations: 16     Fields:    Translation:HumansCells
  88. Aoki M, Warita H, Mizuno H, Suzuki N, Yuki S, Itoyama Y. Feasibility study for functional test battery of SOD transgenic rat (H46R) and evaluation of edaravone, a free radical scavenger. Brain Res. 2011 Mar 25; 1382:321-5. PMID: 21276427.
    Citations: 7     Fields:    Translation:Animals
  89. Kasama S, Ogawa T, Ikawa T, Shigeta Y, Hirai S, Fukushima S, Hattori A, Suzuki N. Influence of metal artifacts on the creation of individual 3D cranio-mandibular models. Stud Health Technol Inform. 2011; 163:261-3. PMID: 21335800.
    Citations:    Fields:    Translation:Humans
  90. Hayashi S, Ohsawa Y, Takahashi T, Suzuki N, Okada T, Rikimaru M, Murakami T, Aoki M, Sunada Y. Rapid screening for Japanese dysferlinopathy by fluorescent primer extension. Intern Med. 2010; 49(24):2693-6. PMID: 21173544.
    Citations: 4     Fields:    Translation:HumansCells
  91. Jeret JS, Suzuki N, Takahashi T, Fujihara K. Neuromyelitis optica preceded by hyperCKemia episode. Neurology. 2010 Dec 14; 75(24):2253 author reply 2253-4. PMID: 21172851.
    Citations: 5     Fields:    Translation:Humans
  92. Izumi R, Suzuki N, Kato K, Warita H, Tateyama M, Nakashima I, Itoyama Y. A case of McArdle disease: efficacy of vitamin B6 on fatigability and impaired glycogenolysis. Intern Med. 2010; 49(15):1623-5. PMID: 20686302.
    Citations: 3     Fields:    Translation:HumansCells
  93. Suzuki N, Mizuno H, Warita H, Takeda S, Itoyama Y, Aoki M. Neuronal NOS is dislocated during muscle atrophy in amyotrophic lateral sclerosis. J Neurol Sci. 2010 Jul 15; 294(1-2):95-101. PMID: 20435320.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  94. Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Mutations of optineurin in amyotrophic lateral sclerosis. Nature. 2010 May 13; 465(7295):223-6. PMID: 20428114.
    Citations: 412     Fields:    Translation:HumansCells
  95. Suzuki N, Aoki M, Warita H, Kato M, Mizuno H, Shimakura N, Akiyama T, Furuya H, Hokonohara T, Iwaki A, Togashi S, Konno H, Itoyama Y. FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion. J Hum Genet. 2010 Apr; 55(4):252-4. PMID: 20224596.
    Citations: 23     Fields:    Translation:HumansCells
  96. Endo K, Suzuki N, Ikenishi T, Aoki M, Itoyama Y. Intravenous immunoglobulin treatment successfully improved subacute progressive polyradiculoneuropathy with polyclonal gammopathy. Intern Med. 2009; 48(23):2037-9. PMID: 19952488.
    Citations:    Fields:    Translation:Humans
  97. Aoki M, Warita H, Suzuki N, Itoyama Y. [Development of motor neuron restorative therapy in amyotrophic lateral sclerosis using hepatocyte growth factor]. Rinsho Shinkeigaku. 2009 Nov; 49(11):814-7. PMID: 20030218.
    Citations:    Fields:    Translation:HumansAnimalsCells
  98. Endo K, Suzuki N, Misu T, Aoki M, Itoyama Y. Dorsal-roots enhancement and Wallerian degeneration of dorsal cord in the patient of acute sensory ataxic neuropathy. J Neurol. 2009 Oct; 256(10):1765-6. PMID: 19479165.
    Citations:    Fields:    Translation:Humans
  99. Ono H, Suzuki N, Mizuno H, Tateyama M, Aoki M, Itoyama Y. [Elevated serum aldolase activity in a patient of non-eosinophilic myofasciitis and synovitis with perifascicular atrophy]. Rinsho Shinkeigaku. 2009 Feb-Mar; 49(2-3):119-22. PMID: 19348178.
    Citations:    Fields:    Translation:Humans
  100. Nezu M, Suzuki N, Mizuno H, Takai Y, Misu T, Aoki M, Nakashima I, Itoyama Y. [Case of Neuro-Behçet disease resembling bacterial meningitis]. Rinsho Shinkeigaku. 2008 Oct; 48(10):750-3. PMID: 19086433.
    Citations:    Fields:    Translation:Humans
  101. Tanihata J, Suzuki N, Miyagoe-Suzuki Y, Imaizumi K, Takeda S. Downstream utrophin enhancer is required for expression of utrophin in skeletal muscle. J Gene Med. 2008 Jun; 10(6):702-13. PMID: 18338831.
    Citations: 2     Fields:    Translation:AnimalsCells
  102. Dagvajantsan B, Aoki M, Warita H, Suzuki N, Itoyama Y. Up-regulation of insulin-like growth factor-II receptor in reactive astrocytes in the spinal cord of amyotrophic lateral sclerosis transgenic rats. Tohoku J Exp Med. 2008 Apr; 214(4):303-10. PMID: 18441505.
    Citations: 7     Fields:    Translation:AnimalsCells
  103. Kato K, Suzuki N, Aoki M, Warita H, Jin K, Itoyama Y. [Massive bleeding from tracheoarterial fistula in an amyotrophic lateral sclerosis patient treated with long-term invasive ventilation: an autopsy case report]. Rinsho Shinkeigaku. 2008 Jan; 48(1):60-2. PMID: 18386635.
    Citations:    Fields:    Translation:Humans
  104. Suzuki S, Suzuki N, Hattori A, Otake Y, Hashizume M. Telecontrol function of an endoscopic surgical robot with two hands for tele-NOTES surgery. Stud Health Technol Inform. 2008; 132:511-3. PMID: 18391358.
    Citations: 1     Fields:    Translation:Humans
  105. Otake Y, Suzuki N, Hattori A, Miki H, Yamamura M, Yonenobu K, Ochi T, Sugano N. Hip motion analysis using multi phase (virtual and physical) simulation of the patient-specific hip joint dynamics. Stud Health Technol Inform. 2008; 132:339-44. PMID: 18391317.
    Citations:    Fields:    Translation:Humans
  106. Saito H, Suzuki N, Ishiguro H, Hirota K, Itoyama Y, Takahashi T, Aoki M. Distal anterior compartment myopathy with early ankle contractures. Muscle Nerve. 2007 Oct; 36(4):525-7. PMID: 17614318.
    Citations: 4     Fields:    Translation:Humans
  107. Suzuki N, Motohashi N, Uezumi A, Fukada S, Yoshimura T, Itoyama Y, Aoki M, Miyagoe-Suzuki Y, Takeda S. NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS. J Clin Invest. 2007 Sep; 117(9):2468-76. PMID: 17786240.
    Citations: 78     Fields:    Translation:AnimalsCells
  108. Suzuki S, Eto K, Hattori A, Yanaga K, Suzuki N. Surgery simulation using patient-specific models for laparoscopic colectomy. Stud Health Technol Inform. 2007; 125:464-6. PMID: 17377327.
    Citations: 6     Fields:    Translation:Humans
  109. Otake Y, Suzuki N, Hattori A, Miki H, Yamamura M, Yonenobu K, Ochi T, Sugano N. System for intraoperative evaluation of soft-tissue-generated forces during total hip arthroplasty by measurement of the pressure distribution in artificial joints. Comput Aided Surg. 2007 Jan; 12(1):53-9. PMID: 17364659.
    Citations:    Fields:    Translation:Humans
  110. Suzuki N, Hattori A, Suzuki S, Otake Y. Development of a surgical robot system for endovascular surgery with augmented reality function. Stud Health Technol Inform. 2007; 125:460-3. PMID: 17377326.
    Citations: 1     Fields:    Translation:Humans
  111. Hayashibe M, Suzuki N, Hattori A, Otake Y, Suzuki S, Nakata N. Surgical navigation display system using volume rendering of intraoperatively scanned CT images. Comput Aided Surg. 2006 Sep; 11(5):240-6. PMID: 17127649.
    Citations: 1     Fields:    Translation:Humans
  112. Hayashibe M, Suzuki N, Hashizume M, Konishi K, Hattori A. Robotic surgery setup simulation with the integration of inverse-kinematics computation and medical imaging. Comput Methods Programs Biomed. 2006 Jul; 83(1):63-72. PMID: 16828195.
    Citations:    Fields:    
  113. Hayashibe M, Suzuki N, Nakamura Y. Laser-scan endoscope system for intraoperative geometry acquisition and surgical robot safety management. Med Image Anal. 2006 Aug; 10(4):509-19. PMID: 16624612.
    Citations: 6     Fields:    Translation:Animals
  114. Otake Y, Suzuki N, Hattori A, Hayashibe M, Miki H, Yamamura M, Sugano N, Yonenobu K, Ochi T. Soft-tissue balance evaluation system for total hip arthroplasty by intraoperative contact pressure measurement at the hip joint. Stud Health Technol Inform. 2006; 119:416-21. PMID: 16404090.
    Citations:    Fields:    Translation:Humans
  115. Suzuki N, Aoki M, Mizuno H, Onodera Y, Takahashi T, Nagata T, Tateyama M, Itoyama Y. Late-onset distal myopathy with rimmed vacuoles without mutation in the GNE or dysferlin genes. Muscle Nerve. 2005 Dec; 32(6):812-4. PMID: 16116644.
    Citations: 2     Fields:    Translation:HumansCells
  116. Kondo C, Mori S, Endo M, Kusakabe K, Suzuki N, Hattori A, Kusakabe M. Real-time volumetric imaging of human heart without electrocardiographic gating by 256-detector row computed tomography: initial experience. J Comput Assist Tomogr. 2005 Sep-Oct; 29(5):694-8. PMID: 16163045.
    Citations: 11     Fields:    Translation:Humans
  117. Suzuki N, Aoki M, Hinuma Y, Takahashi T, Onodera Y, Ishigaki A, Kato M, Warita H, Tateyama M, Itoyama Y. Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL). Neurosci Res. 2005 May; 52(1):47-60. PMID: 15811552.
    Citations: 12     Fields:    Translation:Animals
  118. Otake Y, Suzuki N, Hattori A, Miki H, Yamamura M, Nakamura N, Sugano N, Yonenobu K, Ochi T. Estimation of dislocation after total hip arthroplasty by 4-dimensional. Stud Health Technol Inform. 2005; 111:372-7. PMID: 15718763.
    Citations:    Fields:    Translation:Humans
  119. Suzuki S, Suzuki N, Hayashibe M, Hattori A, Konishi K, Kakeji Y, Hashizume M. Tele-surgical simulation system for training in the use of da Vinci surgery. Stud Health Technol Inform. 2005; 111:543-8. PMID: 15718794.
    Citations: 6     Fields:    Translation:Humans
  120. Hayashibe M, Suzuki N, Hattori A, Suzuki S, Konishi K, Kakeji Y, Hashizume M. Surgical robot setup simulation with consistent kinematics and haptics for abdominal surgery. Stud Health Technol Inform. 2005; 111:164-6. PMID: 15718720.
    Citations: 1     Fields:    Translation:Humans
  121. Hayashibe M, Suzuki N, Kobayashi S, Nakata N, Hattori A, Nakamura Y. Development of a 3D visualization system for surgical field deformation with geometric pattern projection. Stud Health Technol Inform. 2005; 111:172-7. PMID: 15718722.
    Citations: 2     Fields:    
  122. Hattori A, Suzuki N, Hayashibe M, Suzuki S, Otake Y, Tajiri H, Kobayashi S. Development of a navigation function for an endosocopic robot surgery system. Stud Health Technol Inform. 2005; 111:167-71. PMID: 15718721.
    Citations: 1     Fields:    Translation:Humans
  123. Otake Y, Suzuki N, Hattori A, Hagio K, Sugano N, Yonenobu K, Ochi T. Four-dimensional model of the lower extremity after total hip arthroplasty. J Biomech. 2005 Dec; 38(12):2397-405. PMID: 16214487.
    Citations: 1     Fields:    Translation:Humans
  124. Suzuki S, Suzuki N, Hattori A, Uchiyama A, Kobayashi S. Sphere-filled organ model for virtual surgery system. IEEE Trans Med Imaging. 2004 Jun; 23(6):714-22. PMID: 15191146.
    Citations: 2     Fields:    Translation:HumansAnimals
  125. Suzuki N, Aoki M, Takahashi T, Takano D, Asano M, Shiga Y, Onodera Y, Tateyama M, Itoyama Y. Novel dysferlin mutations and characteristic muscle atrophy in late-onset Miyoshi myopathy. Muscle Nerve. 2004 May; 29(5):721-3. PMID: 15116377.
    Citations: 2     Fields:    Translation:Humans
  126. Sumiyama K, Suzuki N, Tajiri H. A linear-array freehand 3-D endoscopic ultrasound. Ultrasound Med Biol. 2003 Jul; 29(7):1001-6. PMID: 12878246.
    Citations:    Fields:    Translation:HumansAnimals
  127. Sanjo A, Satoi J, Ohnishi A, Maruno J, Fukata M, Suzuki N. Role of elevated platelet-associated immunoglobulin G and hypersplenism in thrombocytopenia of chronic liver diseases. J Gastroenterol Hepatol. 2003 Jun; 18(6):638-44. PMID: 12753144.
    Citations: 18     Fields:    Translation:HumansCells
  128. Otake Y, Hagio K, Suzuki N, Hattori A, Sugano N, Yonenobu K, Ochi T. 4-dimensional computer-based motion simulation after Total Hip Arthroplasty. Stud Health Technol Inform. 2003; 94:251-7. PMID: 15455903.
    Citations:    Fields:    Translation:Humans
  129. Hattori A, Suzuki N, Hashizume M, Akahoshi T, Konishi K, Yamaguchi S, Shimada M, Hayashibe M. A robotic surgery system (da Vinci) with image guided function--system architecture and cholecystectomy application. Stud Health Technol Inform. 2003; 94:110-6. PMID: 15455874.
    Citations: 3     Fields:    Translation:Humans
  130. Suzuki N, Hattori A, Hayashibe M, Suzuki S, Otake Y. Development of Dynamic Spatial Video Camera (DSVC) for 4D observation, analysis and modeling of human body locomotion. Stud Health Technol Inform. 2003; 94:346-8. PMID: 15455921.
    Citations:    Fields:    Translation:Humans
  131. Suzuki S, Suzuki N, Hattori A, Uchiyama A. Dynamic deformation of elastic organ model and the VR cockpit for virtual surgery and tele-surgery. Stud Health Technol Inform. 2003; 94:354-6. PMID: 15455923.
    Citations:    Fields:    Translation:Humans
  132. Suzuki N, Jin K, Shiga Y, Kato H, Itoyama Y. [A case of neuralgic amyotrophy manifesting bilateral anterior interosseous nerve syndrome]. No To Shinkei. 2002 Jul; 54(7):605-8. PMID: 12187720.
    Citations:    Fields:    Translation:Humans
  133. Sumiyama K, Suzuki N, Kakutani H, Hino S, Tajiri H, Suzuki H, Aoki T. A novel 3-dimensional EUS technique for real-time visualization of the volume data reconstruction process. Gastrointest Endosc. 2002 May; 55(6):723-8. PMID: 11979259.
    Citations: 1     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.