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Items: 1 to 50 of 126

1.

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
2.

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 Apr 23. doi: 10.1007/s12311-018-0941-6. [Epub ahead of print]

PMID:
29687291
3.

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 Apr 1:1352458518763099. doi: 10.1177/1352458518763099. [Epub ahead of print]

PMID:
29671689
4.

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.

5.

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
6.

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
7.

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
8.

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
9.

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
10.

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
11.

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.

12.

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.

13.

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.

14.

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
15.

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
16.

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.

17.

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
18.

[Literature review of intravascular lymphomatosis].

Koyano S, Hashiguchi S, Tanaka F.

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

PMID:
25082315
19.

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.

20.

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
21.

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.

22.

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
23.
24.

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.

25.

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.

26.

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
27.

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
28.

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.

29.

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.

30.

[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
31.

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
32.

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
33.

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.

34.

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
35.

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
36.

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
37.

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
38.

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
39.

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.

40.

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.

41.

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.

Doi H, Yoshida K, Yasuda T, Fukuda M, Fukuda Y, Morita H, Ikeda S, Kato R, Tsurusaki Y, Miyake N, Saitsu H, Sakai H, Miyatake S, Shiina M, Nukina N, Koyano S, Tsuji S, Kuroiwa Y, Matsumoto N.

Am J Hum Genet. 2011 Aug 12;89(2):320-7. doi: 10.1016/j.ajhg.2011.07.012.

42.

Lupus miliaris disseminatus faciei successfully treated with tranilast: report of two cases.

Koike Y, Hatamochi A, Koyano S, Namikawa H, Hamasaki Y, Yamazaki S.

J Dermatol. 2011 Jun;38(6):588-92. doi: 10.1111/j.1346-8138.2010.01116.x. Epub 2010 Nov 26.

PMID:
21623898
43.

Evaluation of multiplex PCR using dual-priming oligonucleotide for the detection of vanA and vanB in vancomycin-resistant enterococci.

Nagai R, Saito R, Koyano S, Okamura N, Yokota H, Kitazawa T, Moriya K.

Clin Chem Lab Med. 2011 Apr;49(4):751-2. doi: 10.1515/CCLM.2011.103. Epub 2011 Jan 31. No abstract available.

PMID:
21275812
44.

Evaluation of a chromogenic agar medium for the detection of extended-spectrum ß-lactamase-producing Enterobacteriaceae.

Saito R, Koyano S, Nagai R, Okamura N, Moriya K, Koike K.

Lett Appl Microbiol. 2010 Dec;51(6):704-6.

PMID:
21117288
45.

Is annular erythema developing in a pregnant patient with Sjögren's syndrome a predictor of potential neonatal lupus erythematosus in the infant?

Koyano S, Hamasaki Y, Ishikawa S, Yamazaki S, Arai S, Watanabe H, Inaba N, Hatamochi A.

J Dermatol. 2010 Nov;37(11):1000-3. doi: 10.1111/j.1346-8138.2010.00926.x. Review. No abstract available.

PMID:
21039792
46.

[A case of spinocerebellar ataxia type 2 presenting with a clinical course similar to spastic paraparesis].

Miyaji Y, Doi H, Koyano S, Baba Y, Suzuki Y, Kuroiwa Y.

Rinsho Shinkeigaku. 2010 Sep;50(9):641-4. Japanese.

PMID:
20960929
47.

Single cytomegalovirus strain associated with fetal loss and then congenital infection of a subsequent child born to the same mother.

Nagamori T, Koyano S, Inoue N, Yamada H, Oshima M, Minematsu T, Fujieda K.

J Clin Virol. 2010 Oct;49(2):134-6. doi: 10.1016/j.jcv.2010.06.021. Epub 2010 Aug 3.

PMID:
20685160
48.

Changes in the ceramide profile of atopic dermatitis patients.

Ishikawa J, Narita H, Kondo N, Hotta M, Takagi Y, Masukawa Y, Kitahara T, Takema Y, Koyano S, Yamazaki S, Hatamochi A.

J Invest Dermatol. 2010 Oct;130(10):2511-4. doi: 10.1038/jid.2010.161. Epub 2010 Jun 24. No abstract available.

49.

A rare mutation in cystic fibrosis transmembrane conductance regulator gene in a recurrent pancreatitis patient without respiratory symptoms.

Koyano S, Hirano Y, Nagamori T, Tanno S, Murono K, Fujieda K.

Pancreas. 2010 Jul;39(5):686-7. doi: 10.1097/MPA.0b013e3181c65c2e. No abstract available.

PMID:
20562583
50.

Slowly progressive autonomic neuropathy with antiganglionic acetylcholine receptor antibody.

Koike H, Koyano S, Morozumi S, Kawagashira Y, Iijima M, Katsuno M, Hattori N, Vernino S, Sobue G.

J Neurol Neurosurg Psychiatry. 2010 May;81(5):586-7. doi: 10.1136/jnnp.2009.181222. No abstract available.

PMID:
20460600

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