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Items: 1 to 50 of 238

1.

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 Jan 15. doi: 10.1111/neup.12532. [Epub ahead of print]

PMID:
30646429
2.

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
3.

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.

4.

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
5.

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.

6.

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. 2018 Jun 14. doi: 10.1007/s00774-018-0934-z. [Epub ahead of print]

PMID:
29948345
7.

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
8.

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
9.

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
10.

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
11.

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.

12.

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
13.

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.

PMID:
29411683
14.

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
15.

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.

16.

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
17.

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.

18.

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
19.

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.

20.

[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
21.

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
22.

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
23.

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
24.

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.

25.

[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
26.

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.

27.

[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
28.

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
29.

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.

30.

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.

31.

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
32.

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.

33.

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.

34.

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
35.

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
36.

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.

37.

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.

38.

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
39.

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.

40.

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
41.

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
42.

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
43.

Variants associated with Gaucher disease in multiple system atrophy.

Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, Tsuji S.

Ann Clin Transl Neurol. 2015 Apr;2(4):417-26. doi: 10.1002/acn3.185. Epub 2015 Feb 28.

44.

Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems.

Tada M, Nishizawa M, Onodera O.

J Neurol Neurosurg Psychiatry. 2015 Aug;86(8):922-8. doi: 10.1136/jnnp-2013-307225. Epub 2015 Jan 30. Review.

PMID:
25637456
45.

[Aberration of the spliceosome in amyotrophic lateral sclerosis].

Ishihara T, Kakita A, Takahashi H, Onodera O, Nishizawa M.

Rinsho Shinkeigaku. 2014;54(12):1155-7. Review. Japanese.

PMID:
25519968
46.

CARASIL.

Onodera O, Nozaki H, Fukutake T.

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.
2010 Apr 27 [updated 2014 Sep 11].

47.

A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease.

Tamiya G, Makino S, Hayashi M, Abe A, Numakura C, Ueki M, Tanaka A, Ito C, Toshimori K, Ogawa N, Terashima T, Maegawa H, Yanagisawa D, Tooyama I, Tada M, Onodera O, Hayasaka K.

Am J Hum Genet. 2014 Sep 4;95(3):294-300. doi: 10.1016/j.ajhg.2014.07.013. Epub 2014 Aug 21.

48.

Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

Nozaki H, Nishizawa M, Onodera O.

Stroke. 2014 Nov;45(11):3447-53. doi: 10.1161/STROKEAHA.114.004236. Epub 2014 Aug 12. Review. No abstract available.

PMID:
25116877
49.

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.

Yasui K, Yabe I, Yoshida K, Kanai K, Arai K, Ito M, Onodera O, Koyano S, Isozaki E, Sawai S, Adachi Y, Sasaki H, Kuwabara S, Hattori T, Sobue G, Mizusawa H, Tsuji S, Nishizawa M, Nakashima K.

Orphanet J Rare Dis. 2014 Jul 23;9:118. doi: 10.1186/s13023-014-0118-4.

50.

C9ORF72 repeat-associated non-ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9ALS.

Konno T, Tada M, Shiga A, Tsujino A, Eguchi H, Masuda-Suzukake M, Hasegawa M, Nishizawa M, Onodera O, Kakita A, Takahashi H.

Neuropathol Appl Neurobiol. 2014 Oct;40(6):783-8. doi: 10.1111/nan.12157. No abstract available.

PMID:
24861677

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