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Items: 1 to 50 of 245

1.

Spinocerebellar Ataxia Type 17.

Toyoshima Y, Onodera O, Yamada M, Tsuji S, Takahashi H.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2005 Mar 29 [updated 2019 Sep 12].

2.

Shrinkage of the myenteric neurons of the small intestine in patients with multiple system atrophy.

Ozawa T, Shimizu H, Matsui H, Onodera O, Kakita A.

Auton Neurosci. 2019 Aug 22;221:102583. doi: 10.1016/j.autneu.2019.102583. [Epub ahead of print]

PMID:
31476714
3.

HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.

Uemura M, Nozaki H, Koyama A, Sakai N, Ando S, Kanazawa M, Kato T, Onodera O.

Front Neurol. 2019 Jun 28;10:693. doi: 10.3389/fneur.2019.00693. eCollection 2019.

4.

Non-genetically modified models exhibit TARDBP mRNA increase due to perturbed TDP-43 autoregulation.

Sugai A, Kato T, Koyama A, Koike Y, Konno T, Ishihara T, Onodera O.

Neurobiol Dis. 2019 Oct;130:104534. doi: 10.1016/j.nbd.2019.104534. Epub 2019 Jul 13.

PMID:
31310801
5.

Ectopic Expression Induces Abnormal Somatodendritic Distribution of Tau in the Mouse Brain.

Kubo A, Ueda S, Yamane A, Wada-Kakuda S, Narita M, Matsuyama M, Nomori A, Takashima A, Kato T, Onodera O, Goto M, Ito M, Tomiyama T, Mori H, Murayama S, Ihara Y, Misonou H, Miyasaka T.

J Neurosci. 2019 Aug 21;39(34):6781-6797. doi: 10.1523/JNEUROSCI.2845-18.2019. Epub 2019 Jun 24.

PMID:
31235644
6.

Is the population of Sado Island genetically close to the population of western Japan?

Misawa K, Watanabe H, Yokoseki A, Wakasugi M, Onodera O, Narita I, Momotsu T, Sato K, Endo N.

Hum Genome Var. 2019 Jun 4;6:26. doi: 10.1038/s41439-019-0058-6. eCollection 2019.

7.

Angiogenesis in the ischemic core: A potential treatment target?

Kanazawa M, Takahashi T, Ishikawa M, Onodera O, Shimohata T, Del Zoppo GJ.

J Cereb Blood Flow Metab. 2019 May;39(5):753-769. doi: 10.1177/0271678X19834158. Epub 2019 Mar 6.

PMID:
30841779
8.

Duplication and deletion upstream of LMNB1 in autosomal dominant adult-onset leukodystrophy.

Mezaki N, Miura T, Ogaki K, Eriguchi M, Mizuno Y, Komatsu K, Yamazaki H, Suetsugi N, Kawajiri S, Yamasaki R, Ishiguro T, Konno T, Nozaki H, Kasuga K, Okuma Y, Kira JI, Hara H, Onodera O, Ikeuchi T.

Neurol Genet. 2018 Dec 7;4(6):e292. doi: 10.1212/NXG.0000000000000292. eCollection 2018 Dec.

9.

Globular glial tauopathy Type II: Clinicopathological study of two autopsy cases.

Tanaka H, Kawakatsu S, Toyoshima Y, Miura T, Mezaki N, Mano A, Sanpei K, Kobayashi R, Hayashi H, Otani K, Ikeuchi T, Onodera O, Kakita A, Takahashi H.

Neuropathology. 2019 Apr;39(2):111-119. doi: 10.1111/neup.12532. Epub 2019 Jan 15.

PMID:
30646429
10.

Retinal Vasculopathy With Cerebral Leukodystrophy: Clinicopathologic Features of an Autopsied Patient With a Heterozygous TREX 1 Mutation.

Saito R, Nozaki H, Kato T, Toyoshima Y, Tanaka H, Tsubata Y, Morioka T, Horikawa Y, Oyanagi K, Morita T, Onodera O, Kakita A.

J Neuropathol Exp Neurol. 2019 Feb 1;78(2):181-186. doi: 10.1093/jnen/nly115.

PMID:
30561700
11.

Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophy.

Kato K, Maemura R, Wakamatsu M, Yamamori A, Hamada M, Kataoka S, Narita A, Miwata S, Sekiya Y, Kawashima N, Suzuki K, Narita K, Doisaki S, Muramatsu H, Sakaguchi H, Matsumoto K, Koike Y, Onodera O, Kaga M, Shimozawa N, Yoshida N.

Mol Genet Metab Rep. 2018 Nov 20;18:1-6. doi: 10.1016/j.ymgmr.2018.11.001. eCollection 2019 Mar.

12.

Clinicopathologic Features of Two Patients With Sporadic Amyotrophic Lateral Sclerosis Who Maintained Communication Ability for Over 30 Years.

Ito J, Shimada T, Tada M, Shimizu H, Wakabayashi M, Yokoseki A, Onodera O, Takahashi H, Kakita A.

J Neuropathol Exp Neurol. 2018 Nov 1;77(11):981-986. doi: 10.1093/jnen/nly082.

PMID:
30239892
13.

Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.

Miura T, Mezaki N, Konno T, Iwasaki A, Hara N, Miura M, Funayama M, Unai Y, Tashiro Y, Okita K, Kihara T, Ito N, Kanatsuka Y, Jones DT, Hara N, Ishiguro T, Tokutake T, Kasuga K, Nozaki H, Dickson DW, Onodera O, Wszolek ZK, Ikeuchi T.

J Neurol. 2018 Oct;265(10):2415-2424. doi: 10.1007/s00415-018-9017-2. Epub 2018 Aug 22.

14.

Low serum 25-hydroxyvitamin D increases cognitive impairment in elderly people.

Sakuma M, Kitamura K, Endo N, Ikeuchi T, Yokoseki A, Onodera O, Oinuma T, Momotsu T, Sato K, Nakamura K, Narita I.

J Bone Miner Metab. 2019 Mar;37(2):368-375. doi: 10.1007/s00774-018-0934-z. Epub 2018 Jun 14.

PMID:
29948345
15.

CADM1 is a diagnostic marker in early-stage mycosis fungoides: Multicenter study of 58 cases.

Yuki A, Shinkuma S, Hayashi R, Fujikawa H, Kato T, Homma E, Hamade Y, Onodera O, Matsuoka M, Shimizu H, Iwata H, Abe R.

J Am Acad Dermatol. 2018 Dec;79(6):1039-1046. doi: 10.1016/j.jaad.2018.06.025. Epub 2018 Jun 19.

PMID:
29928911
16.

Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation.

Ito J, Nozaki H, Toyoshima Y, Abe T, Sato A, Hashidate H, Igarashi S, Onodera O, Takahashi H, Kakita A.

Neuropathology. 2018 May 25. doi: 10.1111/neup.12473. [Epub ahead of print]

PMID:
29797751
17.

Predictors of cognitive impairment in multiple system atrophy.

Hatakeyama M, Sato T, Takahashi T, Kanazawa M, Onodera O, Nishizawa M, Shimohata T.

J Neurol Sci. 2018 May 15;388:128-132. doi: 10.1016/j.jns.2018.03.017. Epub 2018 Mar 10.

PMID:
29627006
18.

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.

Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S.

Nat Genet. 2018 Apr;50(4):581-590. doi: 10.1038/s41588-018-0067-2. Epub 2018 Mar 5.

PMID:
29507423
19.

Robustness and Vulnerability of the Autoregulatory System That Maintains Nuclear TDP-43 Levels: A Trade-off Hypothesis for ALS Pathology Based on in Silico Data.

Sugai A, Kato T, Koyama A, Koike Y, Kasahara S, Konno T, Ishihara T, Onodera O.

Front Neurosci. 2018 Feb 1;12:28. doi: 10.3389/fnins.2018.00028. eCollection 2018.

20.

Loss of Motor Neurons Innervating Cervical Muscles in Patients With Multiple System Atrophy and Dropped Head.

Saito R, Tada M, Toyoshima Y, Nishizawa M, Onodera O, Takahashi H, Kakita A.

J Neuropathol Exp Neurol. 2018 Apr 1;77(4):317-324. doi: 10.1093/jnen/nly007.

PMID:
29420736
21.

Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease.

Saito N, Ishihara T, Kasuga K, Nishida M, Ishiguro T, Nozaki H, Shimohata T, Onodera O, Nishizawa M.

Prion. 2018 Mar 4;12(2):147-149. doi: 10.1080/19336896.2018.1436926. Epub 2018 Mar 9.

22.

Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosis.

Tohnai G, Nakamura R, Sone J, Nakatochi M, Yokoi D, Katsuno M, Watanabe H, Watanabe H, Ito M, Li Y, Izumi Y, Morita M, Taniguchi A, Kano O, Oda M, Kuwabara S, Abe K, Aiba I, Okamoto K, Mizoguchi K, Hasegawa K, Aoki M, Hattori N, Onodera O, Naruse H, Mitsui J, Takahashi Y, Goto J, Ishiura H, Morishita S, Yoshimura J, Doi K, Tsuji S, Nakashima K, Kaji R, Atsuta N, Sobue G; Japanese Consortium for Amyotrophic Lateral Sclerosis Research (JaCALS).

Neurobiol Aging. 2018 Apr;64:158.e15-158.e19. doi: 10.1016/j.neurobiolaging.2017.12.005. Epub 2017 Dec 11.

PMID:
29398122
23.

Operation of a P300-based brain-computer interface in patients with Duchenne muscular dystrophy.

Utsumi K, Takano K, Okahara Y, Komori T, Onodera O, Kansaku K.

Sci Rep. 2018 Jan 29;8(1):1753. doi: 10.1038/s41598-018-20125-6.

24.

CARASIL families from India with 3 novel null mutations in the HTRA1 gene.

Preethish-Kumar V, Nozaki H, Tiwari S, Vengalil S, Bhat M, Prasad C, Onodera O, Uemura M, Doniparthi S, Saini J, Nashi S, Polavarapu K, Nalini A.

Neurology. 2017 Dec 5;89(23):2392-2394. doi: 10.1212/WNL.0000000000004710. Epub 2017 Nov 3. No abstract available.

PMID:
29101275
25.

New diagnostic criteria for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy in Japan.

Mizuta I, Watanabe-Hosomi A, Koizumi T, Mukai M, Hamano A, Tomii Y, Kondo M, Nakagawa M, Tomimoto H, Hirano T, Uchino M, Onodera O, Mizuno T.

J Neurol Sci. 2017 Oct 15;381:62-67. doi: 10.1016/j.jns.2017.08.009. Epub 2017 Aug 8.

26.

Apparent diffusion coefficient reduction might be a predictor of poor outcome in patients with posterior reversible encephalopathy syndrome.

Ninomiya I, Kanazawa M, Akaiwa Y, Shimohata T, Okamoto K, Onodera O, Nishizawa M.

J Neurol Sci. 2017 Oct 15;381:1-3. doi: 10.1016/j.jns.2017.08.002. Epub 2017 Aug 7.

PMID:
28991655
27.

Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation.

Konno T, Yoshida K, Mizuta I, Mizuno T, Kawarai T, Tada M, Nozaki H, Ikeda SI, Onodera O, Wszolek ZK, Ikeuchi T.

Eur J Neurol. 2018 Jan;25(1):142-147. doi: 10.1111/ene.13464. Epub 2017 Oct 19.

28.

[Overview of Hereditary Spinocerebellar Ataxias in Japan].

Tada M, Yokoseki A, Onodera O.

Brain Nerve. 2017 Aug;69(8):879-890. doi: 10.11477/mf.1416200839. Japanese.

PMID:
28819072
29.

A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review.

Ibrahimi M, Nozaki H, Lee A, Onodera O, Reichwein R, Wicklund M, El-Ghanem M.

Cerebrovasc Dis. 2017;44(3-4):135-140. doi: 10.1159/000477358. Epub 2017 Jun 21. Review.

PMID:
28628911
30.

The Clinical Features, Risk Factors, and Surgical Treatment of Cervicogenic Headache in Patients With Cervical Spine Disorders Requiring Surgery.

Shimohata K, Hasegawa K, Onodera O, Nishizawa M, Shimohata T.

Headache. 2017 Jul;57(7):1109-1117. doi: 10.1111/head.13123. Epub 2017 Jun 5.

PMID:
28581034
31.

Evidence that phosphorylated ubiquitin signaling is involved in the etiology of Parkinson's disease.

Shiba-Fukushima K, Ishikawa KI, Inoshita T, Izawa N, Takanashi M, Sato S, Onodera O, Akamatsu W, Okano H, Imai Y, Hattori N.

Hum Mol Genet. 2017 Aug 15;26(16):3172-3185. doi: 10.1093/hmg/ddx201.

PMID:
28541509
32.

Multiple system atrophy: clinicopathological characteristics in Japanese patients.

Ozawa T, Onodera O.

Proc Jpn Acad Ser B Phys Biol Sci. 2017;93(5):251-258. doi: 10.2183/pjab.93.016. Review.

33.

[PRES: Posterior Reversible Encephalopathy Syndrome].

Okamoto K, Motohashi K, Fujiwara H, Ishihara T, Ninomiya I, Onodera O, Fujii Y.

Brain Nerve. 2017 Feb;69(2):129-141. doi: 10.11477/mf.1416200653. Review. Japanese.

PMID:
28202821
34.

Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats.

Kanazawa M, Miura M, Toriyabe M, Koyama M, Hatakeyama M, Ishikawa M, Nakajima T, Onodera O, Takahashi T, Nishizawa M, Shimohata T.

Sci Rep. 2017 Feb 14;7:42582. doi: 10.1038/srep42582.

35.

[Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL)].

Uemura M, Nozaki H, Onodera O.

Brain Nerve. 2017 Jan;69(1):25-33. doi: 10.11477/mf.1416200631. Japanese.

PMID:
28126975
36.

Association between dialysis treatment and cognitive decline: A study from the Project in Sado for Total Health (PROST), Japan.

Watanabe Y, Kitamura K, Nakamura K, Sanpei K, Wakasugi M, Yokoseki A, Kabasawa K, Onodera O, Ikeuchi T, Kuwano R, Momotsu T, Narita I, Endo N.

Geriatr Gerontol Int. 2017 Oct;17(10):1584-1587. doi: 10.1111/ggi.12937. Epub 2016 Nov 21.

PMID:
27869346
37.

Clinicopathological characteristics of patients with amyotrophic lateral sclerosis resulting in a totally locked-in state (communication Stage V).

Hayashi K, Mochizuki Y, Takeuchi R, Shimizu T, Nagao M, Watabe K, Arai N, Oyanagi K, Onodera O, Hayashi M, Takahashi H, Kakita A, Isozaki E.

Acta Neuropathol Commun. 2016 Sep 30;4(1):107.

38.

Modifiable Factors Associated with Cognitive Impairment in 1,143 Japanese Outpatients: The Project in Sado for Total Health (PROST).

Kitamura K, Watanabe Y, Nakamura K, Sanpei K, Wakasugi M, Yokoseki A, Onodera O, Ikeuchi T, Kuwano R, Momotsu T, Narita I, Endo N.

Dement Geriatr Cogn Dis Extra. 2016 Aug 12;6(2):341-349. eCollection 2016 May-Aug.

39.

Performance of a real-time PCR-based approach and droplet digital PCR in detecting human parechovirus type 3 RNA.

Aizawa Y, Koyama A, Ishihara T, Onodera O, Saitoh A.

J Clin Virol. 2016 Nov;84:27-31. doi: 10.1016/j.jcv.2016.09.009. Epub 2016 Sep 23.

PMID:
27690140
40.

Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.

Konno T, Yoshida K, Mizuno T, Kawarai T, Tada M, Nozaki H, Ikeda SI, Nishizawa M, Onodera O, Wszolek ZK, Ikeuchi T.

Eur J Neurol. 2017 Jan;24(1):37-45. doi: 10.1111/ene.13125. Epub 2016 Sep 29.

41.

Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia.

Konno T, Broderick DF, Mezaki N, Isami A, Kaneda D, Tashiro Y, Tokutake T, Keegan BM, Woodruff BK, Miura T, Nozaki H, Nishizawa M, Onodera O, Wszolek ZK, Ikeuchi T.

AJNR Am J Neuroradiol. 2017 Jan;38(1):77-83. doi: 10.3174/ajnr.A4938. Epub 2016 Sep 15.

42.

Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids.

Tada M, Konno T, Tada M, Tezuka T, Miura T, Mezaki N, Okazaki K, Arakawa M, Itoh K, Yamamoto T, Yokoo H, Yoshikura N, Ishihara K, Horie M, Takebayashi H, Toyoshima Y, Naito M, Onodera O, Nishizawa M, Takahashi H, Ikeuchi T, Kakita A.

Ann Neurol. 2016 Oct;80(4):554-65. doi: 10.1002/ana.24754. Epub 2016 Sep 4.

PMID:
27490250
43.

Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.

Jiang H, Shimizu H, Shiga A, Tanaka M, Onodera O, Kakita A, Takahashi H.

Neuropathology. 2017 Feb;37(1):69-77. doi: 10.1111/neup.12324. Epub 2016 Jul 22.

PMID:
27444855
44.

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes.

Takeuchi R, Tada M, Shiga A, Toyoshima Y, Konno T, Sato T, Nozaki H, Kato T, Horie M, Shimizu H, Takebayashi H, Onodera O, Nishizawa M, Kakita A, Takahashi H.

Acta Neuropathol Commun. 2016 Jun 23;4(1):61. doi: 10.1186/s40478-016-0335-2.

45.

Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43.

Koyama A, Sugai A, Kato T, Ishihara T, Shiga A, Toyoshima Y, Koyama M, Konno T, Hirokawa S, Yokoseki A, Nishizawa M, Kakita A, Takahashi H, Onodera O.

Nucleic Acids Res. 2016 Jul 8;44(12):5820-36. doi: 10.1093/nar/gkw499. Epub 2016 Jun 2.

46.

Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.

Nozaki H, Kato T, Nihonmatsu M, Saito Y, Mizuta I, Noda T, Koike R, Miyazaki K, Kaito M, Ito S, Makino M, Koyama A, Shiga A, Uemura M, Sekine Y, Murakami A, Moritani S, Hara K, Yokoseki A, Kuwano R, Endo N, Momotsu T, Yoshida M, Nishizawa M, Mizuno T, Onodera O.

Neurology. 2016 May 24;86(21):1964-74. doi: 10.1212/WNL.0000000000002694. Epub 2016 Apr 27.

PMID:
27164673
47.

Elevated C-Reactive Protein Is Associated with Cognitive Decline in Outpatients of a General Hospital: The Project in Sado for Total Health (PROST).

Watanabe Y, Kitamura K, Nakamura K, Sanpei K, Wakasugi M, Yokoseki A, Onodera O, Ikeuchi T, Kuwano R, Momotsu T, Narita I, Endo N.

Dement Geriatr Cogn Dis Extra. 2016 Jan 19;6(1):10-9. doi: 10.1159/000442585. eCollection 2016 Jan-Apr.

48.

Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias.

Tada M, Nishizawa M, Onodera O.

Neurochem Int. 2016 Mar;94:1-8. doi: 10.1016/j.neuint.2016.01.007. Epub 2016 Jan 28. Review.

PMID:
26827887
49.

Characteristic features and progression of abnormalities on MRI for CARASIL.

Nozaki H, Sekine Y, Fukutake T, Nishimoto Y, Shimoe Y, Shirata A, Yanagawa S, Hirayama M, Tamura M, Nishizawa M, Onodera O.

Neurology. 2015 Aug 4;85(5):459-63. doi: 10.1212/WNL.0000000000001803. Epub 2015 Jul 2.

PMID:
26138950
50.

Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.

Yokoyama Y, Toyoshima Y, Shiga A, Tada M, Kitamura H, Hasegawa K, Onodera O, Ikeuchi T, Someya T, Nishizawa M, Kakita A, Takahashi H.

Brain Pathol. 2016 Mar;26(2):155-66. doi: 10.1111/bpa.12265. Epub 2015 Jun 4.

PMID:
25974705

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