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Items: 1 to 50 of 136

1.

Adult-onset vocal cord paralysis in slow-channel congenital myasthenic syndrome.

Nakamura H, Komiya H, Uematsu E, Nakae Y, Tanaka K, Kunii M, Tada M, Joki H, Koyano S, Matsumoto N, Doi H, Takeuchi H, Tanaka F.

Neurol Clin Pract. 2019 Oct;9(5):e45-e47. doi: 10.1212/CPJ.0000000000000599. No abstract available.

PMID:
31750034
2.

Proteomic analysis of exosome-enriched fractions derived from cerebrospinal fluid of amyotrophic lateral sclerosis patients.

Hayashi N, Doi H, Kurata Y, Kagawa H, Atobe Y, Funakoshi K, Tada M, Katsumoto A, Tanaka K, Kunii M, Nakamura H, Takahashi K, Takeuchi H, Koyano S, Kimura Y, Hirano H, Tanaka F.

Neurosci Res. 2019 Oct 24. pii: S0168-0102(19)30487-0. doi: 10.1016/j.neures.2019.10.010. [Epub ahead of print]

PMID:
31669371
3.

Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.

Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, Takeuchi H, Kawamoto M, Kohara N, Ando T, Ieda T, Kita Y, Kokubun N, Tsuboi Y, Katoh K, Kino Y, Katsuno M, Iwasaki Y, Yoshida M, Tanaka F, Suzuki IK, Frith MC, Matsumoto N, Sobue G.

Nat Genet. 2019 Aug;51(8):1215-1221. doi: 10.1038/s41588-019-0459-y. Epub 2019 Jul 22.

PMID:
31332381
4.

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42.

Hashiguchi S, Doi H, Kunii M, Nakamura Y, Shimuta M, Suzuki E, Koyano S, Okubo M, Kishida H, Shiina M, Ogata K, Hirashima F, Inoue Y, Kubota S, Hayashi N, Nakamura H, Takahashi K, Katsumoto A, Tada M, Tanaka K, Sasaoka T, Miyatake S, Miyake N, Saitsu H, Sato N, Ozaki K, Ohta K, Yokota T, Mizusawa H, Mitsui J, Ishiura H, Yoshimura J, Morishita S, Tsuji S, Takeuchi H, Ishikawa K, Matsumoto N, Ishikawa T, Tanaka F.

Neurobiol Dis. 2019 Oct;130:104516. doi: 10.1016/j.nbd.2019.104516. Epub 2019 Jun 20.

PMID:
31229688
5.

Novel VRK1 Mutations in a Patient with Childhood-onset Motor Neuron Disease.

Yamaura G, Higashiyama Y, Kusama K, Kunii M, Tanaka K, Koyano S, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Iwahashi Y, Joki H, Matsumoto N, Doi H, Tanaka F.

Intern Med. 2019 Sep 15;58(18):2715-2719. doi: 10.2169/internalmedicine.2126-18. Epub 2019 Jun 7.

6.

Evaluation of the indirect and IgM-capture anti-human cytomegalovirus IgM ELISA methods as confirmed by cytomegalovirus IgG avidity.

Ikuta K, Koshizuka T, Kanno R, Inoue N, Kubo T, Koyano S, Suzutani T.

Microbiol Immunol. 2019 May;63(5):172-178. doi: 10.1111/1348-0421.12683. Epub 2019 May 22.

PMID:
31012489
7.

Concentrations of POPs based wood preservatives in waste timber from demolished buildings and its recycled products in Japan.

Koyano S, Ueno D, Yamamoto T, Kajiwara N.

Waste Manag. 2019 Feb 15;85:445-451. doi: 10.1016/j.wasman.2018.12.039. Epub 2019 Jan 16.

PMID:
30803600
8.

A Case of McLeod Syndrome with A Novel XK Missense Mutation.

Komiya H, Takasu M, Hashiguchi S, Uematsu E, Fukai R, Tanaka K, Tada M, Joki H, Takahashi T, Koyano S, Doi H, Takeuchi H, Tanaka F.

Mov Disord Clin Pract. 2018 Apr 6;5(3):333-336. doi: 10.1002/mdc3.12614. eCollection 2018 May-Jun. No abstract available.

9.

Genetic characterization of Lassa virus strains isolated from 2012 to 2016 in southeastern Nigeria.

Oloniniyi OK, Unigwe US, Okada S, Kimura M, Koyano S, Miyazaki Y, Iroezindu MO, Ajayi NA, Chukwubike CM, Chika-Igwenyi NM, Ndu AC, Nwidi DU, Abe H, Urata S, Kurosaki Y, Yasuda J.

PLoS Negl Trop Dis. 2018 Nov 30;12(11):e0006971. doi: 10.1371/journal.pntd.0006971. eCollection 2018 Nov.

10.

Genetic analysis of adult leukoencephalopathy patients using a custom-designed gene panel.

Kunii M, Doi H, Ishii Y, Ohba C, Tanaka K, Tada M, Fukai R, Hashiguchi S, Kishida H, Ueda N, Kudo Y, Kugimoto C, Nakano T, Udaka N, Miyatake S, Miyake N, Saitsu H, Ito Y, Takahashi K, Nakamura H, Tomita-Katsumoto A, Takeuchi H, Koyano S, Matsumoto N, Tanaka F.

Clin Genet. 2018 Aug;94(2):232-238. doi: 10.1111/cge.13371. Epub 2018 Jun 8.

PMID:
29700822
11.

A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies.

Yahikozawa H, Miyatake S, Sakai T, Uehara T, Yamada M, Hanyu N, Futatsugi Y, Doi H, Koyano S, Tanaka F, Suzuki A, Matsumoto N, Yoshida K.

Cerebellum. 2018 Oct;17(5):525-530. doi: 10.1007/s12311-018-0941-6.

PMID:
29687291
12.

Two cases of anaphylactic shock by methylprednisolone in neuromyelitis optica.

Takahashi K, Asano T, Higashiyama Y, Koyano S, Doi H, Takeuchi H, Tanaka F.

Mult Scler. 2018 Oct;24(11):1514-1516. doi: 10.1177/1352458518763099. Epub 2018 Apr 19.

PMID:
29671689
13.

Cerebrospinal fluid level of Nogo receptor 1 antagonist lateral olfactory tract usher substance (LOTUS) correlates inversely with the extent of neuroinflammation.

Takahashi K, Takeuchi H, Kurihara Y, Doi H, Kunii M, Tanaka K, Nakamura H, Fukai R, Tomita-Katsumoto A, Tada M, Higashiyama Y, Joki H, Koyano S, Takei K, Tanaka F.

J Neuroinflammation. 2018 Feb 17;15(1):46. doi: 10.1186/s12974-018-1084-x.

14.

White matter hyperintensities on MRI in dementia with Lewy bodies, Parkinson's disease with dementia, and Alzheimer's disease.

Joki H, Higashiyama Y, Nakae Y, Kugimoto C, Doi H, Kimura K, Kishida H, Ueda N, Nakano T, Takahashi T, Koyano S, Takeuchi H, Tanaka F.

J Neurol Sci. 2018 Feb 15;385:99-104. doi: 10.1016/j.jns.2017.12.018. Epub 2017 Dec 19.

PMID:
29406924
15.

Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations.

Doi H, Koyano S, Miyatake S, Nakajima S, Nakazawa Y, Kunii M, Tomita-Katsumoto A, Oda K, Yamaguchi Y, Fukai R, Ikeda S, Kato R, Ogata K, Kubota S, Hayashi N, Takahashi K, Tada M, Tanaka K, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Ogi T, Aihara M, Takeuchi H, Matsumoto N, Tanaka F.

J Hum Genet. 2018 Apr;63(4):417-423. doi: 10.1038/s10038-017-0408-5. Epub 2018 Feb 5.

PMID:
29403087
16.

Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis.

Tada M, Doi H, Koyano S, Kubota S, Fukai R, Hashiguchi S, Hayashi N, Kawamoto Y, Kunii M, Tanaka K, Takahashi K, Ogawa Y, Iwata R, Yamanaka S, Takeuchi H, Tanaka F.

Am J Pathol. 2018 Feb;188(2):507-514. doi: 10.1016/j.ajpath.2017.10.007. Epub 2017 Nov 9.

PMID:
29128563
17.

Congenital cytomegalovirus in Japan: More than 2 year follow up of infected newborns.

Koyano S, Morioka I, Oka A, Moriuchi H, Asano K, Ito Y, Yoshikawa T, Yamada H, Suzutani T, Inoue N; Japanese Congenital Cytomegalovirus Study Group.

Pediatr Int. 2018 Jan;60(1):57-62. doi: 10.1111/ped.13433. Epub 2017 Dec 19.

PMID:
29032597
18.

Newborn Congenital Cytomegalovirus Screening Based on Clinical Manifestations and Evaluation of DNA-based Assays for In Vitro Diagnostics.

Fujii T, Oka A, Morioka I, Moriuchi H, Koyano S, Yamada H, Saito S, Sameshima H, Nagamatsu T, Tsuchida S, Inoue N; Japanese Congenital Cytomegalovirus Study Group.

Pediatr Infect Dis J. 2017 Oct;36(10):942-946. doi: 10.1097/INF.0000000000001630.

PMID:
28471866
19.

Whole genome analysis on the genetic backgrounds associated with the secondary failure to etanercept in patients with rheumatoid arthritis.

Funahashi K, Koyano S, Echizen H, Matsubara T.

Mod Rheumatol. 2017 Mar;27(2):271-277. doi: 10.1080/14397595.2016.1206172. Epub 2016 Jul 14.

PMID:
27416107
20.

Scedosporium prolificans Endocarditis: Case Report and Literature Review.

Wakabayashi Y, Okugawa S, Tatsuno K, Ikeda M, Misawa Y, Koyano S, Tsuji E, Yanagimoto S, Hatakeyama S, Moriya K, Yotsuyanagi H.

Intern Med. 2016;55(1):79-82. doi: 10.2169/internalmedicine.55.5592. Review.

21.

Surveys of Viruliferous Alate Aphid of Plum pox virus in Prunus mume Orchards in Japan.

Kimura K, Usugi T, Hoshi H, Kato A, Ono T, Koyano S, Kagiwada S, Nishio T, Tsuda S.

Plant Dis. 2016 Jan;100(1):40-48. doi: 10.1094/PDIS-05-15-0540-RE. Epub 2015 Nov 11.

PMID:
30688586
22.

Interleukin 10 Level in the Cerebrospinal Fluid as a Possible Biomarker for Lymphomatosis Cerebri.

Hashiguchi S, Momoo T, Murohashi Y, Endo M, Shimamura M, Kawasaki T, Kanada S, Nozawa A, Tada M, Koyano S, Tanaka F.

Intern Med. 2015;54(12):1547-52. doi: 10.2169/internalmedicine.54.3283. Epub 2015 Jun 15.

23.

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.

24.

A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease.

Taniguchi R, Koyano S, Suzutani T, Goishi K, Ito Y, Morioka I, Nakamura H, Yamada H, Oka A, Inoue N.

Infection. 2015 Jun;43(3):353-9. doi: 10.1007/s15010-015-0774-x. Epub 2015 Apr 10.

PMID:
25861030
25.

An Aerodynamic Study of Phonations in Patients With Parkinson Disease (PD).

Ikui Y, Nakamura H, Sano D, Hyakusoku H, Kishida H, Kudo Y, Joki H, Koyano S, Yamauchi A, Takano S, Tayama N, Hirose H, Oridate N, Tanaka F.

J Voice. 2015 May;29(3):273-80. doi: 10.1016/j.jvoice.2014.08.012. Epub 2015 Mar 17.

PMID:
25795370
26.

A Case of Liver Abscess with Desulfovibrio desulfuricans Bacteremia.

Koyano S, Tatsuno K, Okazaki M, Ohkusu K, Sasaki T, Saito R, Okugawa S, Moriya K.

Case Rep Infect Dis. 2015;2015:354168. doi: 10.1155/2015/354168. Epub 2015 Jan 8.

27.

Evaluation of a simple phenotypic method for the detection of carbapenemase-producing Enterobacteriaceae.

Saito R, Koyano S, Dorin M, Higurashi Y, Misawa Y, Nagano N, Kaneko T, Moriya K.

J Microbiol Methods. 2015 Jan;108:45-8. doi: 10.1016/j.mimet.2014.11.008. Epub 2014 Nov 20.

PMID:
25451461
28.

[Literature review of intravascular lymphomatosis].

Koyano S, Hashiguchi S, Tanaka F.

Brain Nerve. 2014 Aug;66(8):927-46. Review. Japanese.

PMID:
25082315
29.

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.

30.

Diversity of vancomycin-resistant enterococci in a low endemicity area.

Suzuki M, Koyano S, Okugawa S, Okazaki M, Seki G, Moriya K.

J Glob Antimicrob Resist. 2014 Jun;2(2):115-118. doi: 10.1016/j.jgar.2014.02.001. Epub 2014 Feb 22.

PMID:
27873589
31.

Construction of a scoring system for predicting the risk of severe gastrointestinal involvement in Henoch-Schönlein Purpura.

Nagamori T, Oka H, Koyano S, Takahashi H, Oki J, Sato Y, Murono K, Iseki K, Takeguchi R, Takeda T, Sato M, Sugai R, Kitamura H, Kajino H, Miura Y, Ishioka T, Azuma H.

Springerplus. 2014 Apr 2;3:171. doi: 10.1186/2193-1801-3-171. eCollection 2014.

32.

Quantitative analysis of upper-limb ataxia in patients with spinocerebellar degeneration.

Ueda N, Hakii Y, Koyano S, Higashiyama Y, Joki H, Baba Y, Suzuki Y, Kuroiwa Y, Tanaka F.

J Neurol. 2014 Jul;261(7):1381-6. doi: 10.1007/s00415-014-7353-4. Epub 2014 Apr 30.

PMID:
24781836
33.
34.

First report of KPC-2 Carbapenemase-producing Klebsiella pneumoniae in Japan.

Saito R, Takahashi R, Sawabe E, Koyano S, Takahashi Y, Shima M, Ushizawa H, Fujie T, Tosaka N, Kato Y, Moriya K, Tohda S, Tojo N, Koike R, Kubota T.

Antimicrob Agents Chemother. 2014 May;58(5):2961-3. doi: 10.1128/AAC.02072-13. Epub 2014 Feb 24.

35.

Virological analysis of a regional mumps outbreak in the northern island of Japan-mumps virus genotyping and clinical description.

Okajima K, Iseki K, Koyano S, Kato A, Azuma H.

Jpn J Infect Dis. 2013;66(6):561-3. No abstract available.

36.

Antimicrobial susceptibility and mechanisms of high-level macrolide resistance in clinical isolates of Moraxella nonliquefaciens.

Nonaka S, Matsuzaki K, Kazama T, Nishiyama H, Ida Y, Koyano S, Sonobe K, Okamura N, Saito R.

J Med Microbiol. 2014 Feb;63(Pt 2):242-7. doi: 10.1099/jmm.0.061788-0. Epub 2013 Nov 6.

PMID:
24196134
37.

Cytomegalovirus (CMV) glycoprotein H-based serological analysis in Japanese healthy pregnant women, and in neonates with congenital CMV infection and their mothers.

Ikuta K, Minematsu T, Inoue N, Kubo T, Asano K, Ishibashi K, Imamura T, Nakai H, Yoshikawa T, Moriuchi H, Fujiwara S, Koyano S, Suzutani T.

J Clin Virol. 2013 Oct;58(2):474-8. doi: 10.1016/j.jcv.2013.07.004. Epub 2013 Aug 1.

PMID:
23916379
38.

Polymorphisms in TLR-2 are associated with congenital cytomegalovirus (CMV) infection but not with congenital CMV disease.

Taniguchi R, Koyano S, Suzutani T, Goishi K, Ito Y, Morioka I, Oka A, Nakamura H, Yamada H, Igarashi T, Inoue N.

Int J Infect Dis. 2013 Dec;17(12):e1092-7. doi: 10.1016/j.ijid.2013.06.004. Epub 2013 Jul 29.

39.

Identification of a novel homozygous SPG7 mutation in a Japanese patient with spastic ataxia: making an efficient diagnosis using exome sequencing for autosomal recessive cerebellar ataxia and spastic paraplegia.

Doi H, Ohba C, Tsurusaki Y, Miyatake S, Miyake N, Saitsu H, Kawamoto Y, Yoshida T, Koyano S, Suzuki Y, Kuroiwa Y, Tanaka F, Matsumoto N.

Intern Med. 2013;52(14):1629-33. Epub 2013 Jul 15.

40.

[Personal genome analysis in amyotrophic lateral sclerosis].

Tanaka F, Sone J, Atsuta N, Nakamura R, Doi H, Koyano S, Sobue G.

Brain Nerve. 2013 Mar;65(3):257-65. Review. Japanese.

PMID:
23475517
41.

A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy.

Higashiyama Y, Doi H, Wakabayashi M, Tsurusaki Y, Miyake N, Saitsu H, Ohba C, Fukai R, Miyatake S, Joki H, Koyano S, Suzuki Y, Tanaka F, Kuroiwa Y, Matsumoto N.

Mov Disord. 2013 Apr;28(4):552-3. doi: 10.1002/mds.25296. Epub 2013 Jan 16. No abstract available.

PMID:
23325613
42.

Molecular characterization of carbapenemase-producing clinical isolates of Enterobacteriaceae in a teaching hospital, Japan.

Koyano S, Saito R, Nagai R, Tatsuno K, Okugawa S, Okamura N, Moriya K.

J Med Microbiol. 2013 Mar;62(Pt 3):446-50. doi: 10.1099/jmm.0.050708-0. Epub 2012 Nov 15.

PMID:
23161765
43.

Characteristics of intestinal pseudo-obstruction in patients with mitochondrial diseases.

Sekino Y, Inamori M, Yamada E, Ohkubo H, Sakai E, Higurashi T, Iida H, Hosono K, Endo H, Nonaka T, Takahashi H, Koide T, Abe Y, Gotoh E, Koyano S, Kuroiwa Y, Maeda S, Nakajima A.

World J Gastroenterol. 2012 Sep 7;18(33):4557-62. doi: 10.3748/wjg.v18.i33.4557.

44.

Newborn screening of congenital cytomegalovirus infection using saliva can be influenced by breast feeding.

Koyano S, Inoue N, Nagamori T, Moriuchi H, Azuma H.

Arch Dis Child Fetal Neonatal Ed. 2013 Mar;98(2):F182. doi: 10.1136/archdischild-2012-302230. Epub 2012 Aug 8. No abstract available.

PMID:
22874907
45.

Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease.

Miyatake S, Miyake N, Touho H, Nishimura-Tadaki A, Kondo Y, Okada I, Tsurusaki Y, Doi H, Sakai H, Saitsu H, Shimojima K, Yamamoto T, Higurashi M, Kawahara N, Kawauchi H, Nagasaka K, Okamoto N, Mori T, Koyano S, Kuroiwa Y, Taguri M, Morita S, Matsubara Y, Kure S, Matsumoto N.

Neurology. 2012 Mar 13;78(11):803-10. doi: 10.1212/WNL.0b013e318249f71f. Epub 2012 Feb 29.

PMID:
22377813
46.

The spectrum of clinicopathological features in pure autonomic neuropathy.

Koike H, Hashimoto R, Tomita M, Kawagashira Y, Iijima M, Koyano S, Momoo T, Yuasa H, Mitake S, Higashihara M, Kaida K, Yamamoto D, Hisahara S, Shimohama S, Nakae Y, Johkura K, Vernino S, Sobue G.

J Neurol. 2012 Oct;259(10):2067-75. doi: 10.1007/s00415-012-6458-x. Epub 2012 Feb 24.

PMID:
22361978
47.

Acoustic characteristics of ataxic speech in Japanese patients with spinocerebellar degeneration (SCD).

Ikui Y, Tsukuda M, Kuroiwa Y, Koyano S, Hirose H, Taguchi T.

Int J Lang Commun Disord. 2012 Jan-Feb;47(1):84-94. doi: 10.1111/j.1460-6984.2011.00083.x. Epub 2011 Nov 18.

PMID:
22268904
48.

Sequential changes in pathophysiology of systemic inflammatory response in a disseminated neonatal herpes simplex virus (HSV) infection.

Nagamori T, Koyano S, Asai Y, Nohara F, Okamoto T, Nagaya K, Hayashi T, Miura Y, Tsuda N, Iseki K, Azuma H.

J Clin Virol. 2012 Mar;53(3):265-7. doi: 10.1016/j.jcv.2011.12.017. Epub 2012 Jan 10.

PMID:
22237001
49.

A novel real-time PCR method for determination and quantification of each cytomegalovirus glycoprotein H subtype in clinical samples.

Ikuta K, Ishioka K, Sato Y, Imamura T, Asano K, Koyano S, Inoue N, Suzutani T.

J Clin Microbiol. 2012 Feb;50(2):499-501. doi: 10.1128/JCM.06032-11. Epub 2011 Nov 23.

50.

Screening for congenital cytomegalovirus infection using newborn urine samples collected on filter paper: feasibility and outcomes from a multicentre study.

Koyano S, Inoue N, Oka A, Moriuchi H, Asano K, Ito Y, Yamada H, Yoshikawa T, Suzutani T; Japanese Congenital Cytomegalovirus Study Group.

BMJ Open. 2011 Jul 29;1(1):e000118. doi: 10.1136/bmjopen-2011-000118.

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