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Items: 1 to 50 of 77

1.

A case of overlapping adult-onset linear scleroderma and Parry-Romberg syndrome presenting with widespread ipsilateral neurogenic involvement.

Yamasaki R, Yonekawa T, Inamizu S, Shinoda K, Ochi H, Matsushita T, Isobe N, Tsuji G, Sadashima S, Kuma Y, Oda Y, Iwaki T, Furue M, Kira JI.

Neuropathology. 2019 Nov 27. doi: 10.1111/neup.12614. [Epub ahead of print]

PMID:
31775183
2.

Fulminant hepatitis and elevated levels of sIL-2R in thyroid storm.

Tanaka Y, Uchida T, Yamaguchi H, Kudo Y, Yonekawa T, Nakazato M.

Endocrinol Diabetes Metab Case Rep. 2019 Sep 27;2019. pii: EDM190078. doi: 10.1530/EDM-19-0078. [Epub ahead of print]

3.

Elevated levels of circulating fibroblast growth factor 23 with hypercalcemia following discontinuation of denosumab.

Uchida T, Yamaguchi H, Kushima C, Yonekawa T, Nakazato M.

Endocr J. 2019 Sep 13. doi: 10.1507/endocrj.EJ19-0198. [Epub ahead of print]

4.

A 24-Week Anemia Correction Study of Daprodustat in Japanese Dialysis Patients.

Tsubakihara Y, Akizawa T, Nangaku M, Onoue T, Yonekawa T, Matsushita H, Endo Y, Cobitz A.

Ther Apher Dial. 2019 Jul 15. doi: 10.1111/1744-9987.12962. [Epub ahead of print]

PMID:
31306555
5.

Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma.

Beltrán D, Anderson ME, Bharathy N, Settelmeyer TP, Svalina MN, Bajwa Z, Shern JF, Gultekin SH, Cuellar MA, Yonekawa T, Keller C, Campbell KP.

Skelet Muscle. 2019 May 4;9(1):11. doi: 10.1186/s13395-019-0195-0.

6.

A novel model for treatment of hypertrophic pachymeningitis.

Cui Y, Masaki K, Zhang X, Yamasaki R, Fujii T, Ogata H, Hayashida S, Yamaguchi H, Hyodo F, Eto H, Koyama S, Iinuma K, Yonekawa T, Matsushita T, Yoshida M, Yamada K, Kawano M, Malissen M, Malissen B, Kira J.

Ann Clin Transl Neurol. 2019 Jan 15;6(3):431-444. doi: 10.1002/acn3.715. eCollection 2019 Mar.

7.

Rapid pleural effusion after discontinuation of lenvatinib in a patient with pleural metastasis from thyroid cancer.

Uchida T, Yamaguchi H, Nagamine K, Yonekawa T, Nakamura E, Shibata N, Kawano F, Asada Y, Nakazato M.

Endocrinol Diabetes Metab Case Rep. 2019 Mar 18;2019. pii: EDM180158. doi: 10.1530/EDM-18-0158. [Epub ahead of print]

8.

Identifying drug substances of screening tool for older persons' appropriate prescriptions for Japanese.

Nomura K, Kojima T, Ishii S, Yonekawa T, Akishita M, Akazawa M.

BMC Geriatr. 2018 Jul 3;18(1):154. doi: 10.1186/s12877-018-0835-y.

9.

Acetylcholine receptor antibody-positive myasthenia gravis associated with small-cell lung cancer: A case report.

Yamasaki M, Funaishi K, Saito N, Yonekawa T, Yamawaki T, Ihara D, Daido W, Ishiyama S, Deguchi N, Taniwaki M, Hattori N.

Medicine (Baltimore). 2018 Apr;97(17):e0541. doi: 10.1097/MD.0000000000010541.

10.

Conformational Change in the Ligand-Binding Pocket via a KISS1R Mutation (P147L) Leads to Isolated Gonadotropin-Releasing Hormone Deficiency.

Shimizu K, Yonekawa T, Yoshida M, Miyazato M, Miura A, Sakoda H, Yamaguchi H, Nakazato M.

J Endocr Soc. 2017 Sep 5;1(10):1259-1271. doi: 10.1210/js.2017-00277. eCollection 2017 Oct 1.

11.

Transgenic Monkey Model of the Polyglutamine Diseases Recapitulating Progressive Neurological Symptoms.

Tomioka I, Ishibashi H, Minakawa EN, Motohashi HH, Takayama O, Saito Y, Popiel HA, Puentes S, Owari K, Nakatani T, Nogami N, Yamamoto K, Noguchi S, Yonekawa T, Tanaka Y, Fujita N, Suzuki H, Kikuchi H, Aizawa S, Nagano S, Yamada D, Nishino I, Ichinohe N, Wada K, Kohsaka S, Nagai Y, Seki K.

eNeuro. 2017 Mar 28;4(2). pii: ENEURO.0250-16.2017. doi: 10.1523/ENEURO.0250-16.2017. eCollection 2017 Mar-Apr.

12.

Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele.

Zhu W, Mitsuhashi S, Yonekawa T, Noguchi S, Huei JC, Nalini A, Preethish-Kumar V, Yamamoto M, Murakata K, Mori-Yoshimura M, Kamada S, Yahikozawa H, Karasawa M, Kimura S, Yamashita F, Nishino I.

J Hum Genet. 2017 Feb;62(2):159-166. doi: 10.1038/jhg.2016.134. Epub 2016 Nov 10.

PMID:
27829678
13.

Early and extensive spinal white matter involvement in neuromyelitis optica.

Hayashida S, Masaki K, Yonekawa T, Suzuki SO, Hiwatashi A, Matsushita T, Watanabe M, Yamasaki R, Suenaga T, Iwaki T, Murai H, Kira JI.

Brain Pathol. 2017 May;27(3):249-265. doi: 10.1111/bpa.12386. Epub 2016 Jun 29.

PMID:
27082714
14.

The association between olfactory bulb volume, cognitive dysfunction, physical disability and depression in multiple sclerosis.

Yaldizli Ö, Penner IK, Yonekawa T, Naegelin Y, Kuhle J, Pardini M, Chard DT, Stippich C, Kira JI, Bendfeldt K, Amann M, Radue EW, Kappos L, Sprenger T.

Eur J Neurol. 2016 Mar;23(3):510-9. doi: 10.1111/ene.12891. Epub 2015 Nov 19.

PMID:
26699999
15.

Hepatitis C virus infection in inclusion body myositis: A case-control study.

Uruha A, Noguchi S, Hayashi YK, Tsuburaya RS, Yonekawa T, Nonaka I, Nishino I.

Neurology. 2016 Jan 19;86(3):211-7. doi: 10.1212/WNL.0000000000002291. Epub 2015 Dec 18.

PMID:
26683644
16.

Copy number variations in multiple sclerosis and neuromyelitis optica.

Sato S, Yamamoto K, Matsushita T, Isobe N, Kawano Y, Iinuma K, Niino M, Fukazawa T, Nakamura Y, Watanabe M, Yonekawa T, Masaki K, Yoshimura S, Murai H, Yamasaki R, Kira J; Japan Multiple Sclerosis Genetics Consortium.

Ann Neurol. 2015 Nov;78(5):762-74. doi: 10.1002/ana.24511. Epub 2015 Sep 18.

PMID:
26296936
17.

Epidemiology of anorexia nervosa in Japanese adolescents.

Hotta M, Horikawa R, Mabe H, Yokoyama S, Sugiyama E, Yonekawa T, Nakazato M, Okamoto Y, Ohara C, Ogawa Y.

Biopsychosoc Med. 2015 Aug 14;9:17. doi: 10.1186/s13030-015-0044-2. eCollection 2015.

18.

RIP1 negatively regulates basal autophagic flux through TFEB to control sensitivity to apoptosis.

Yonekawa T, Gamez G, Kim J, Tan AC, Thorburn J, Gump J, Thorburn A, Morgan MJ.

EMBO Rep. 2015 Jun;16(6):700-8. doi: 10.15252/embr.201439496. Epub 2015 Apr 23.

19.

A nationwide survey of combined central and peripheral demyelination in Japan.

Ogata H, Matsuse D, Yamasaki R, Kawamura N, Matsushita T, Yonekawa T, Hirotani M, Murai H, Kira J.

J Neurol Neurosurg Psychiatry. 2016 Jan;87(1):29-36. doi: 10.1136/jnnp-2014-309831. Epub 2015 Feb 11.

PMID:
25673872
20.

Extremely severe complicated spastic paraplegia 3A with neonatal onset.

Yonekawa T, Oya Y, Higuchi Y, Hashiguchi A, Takashima H, Sugai K, Sasaki M.

Pediatr Neurol. 2014 Nov;51(5):726-9. doi: 10.1016/j.pediatrneurol.2014.07.027. Epub 2014 Jul 24.

PMID:
25193411
21.

Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies.

Suzuki S, Yonekawa T, Kuwana M, Hayashi YK, Okazaki Y, Kawaguchi Y, Suzuki N, Nishino I.

J Neuroimmunol. 2014 Sep 15;274(1-2):202-8. doi: 10.1016/j.jneuroim.2014.07.006. Epub 2014 Jul 17.

PMID:
25064497
22.

Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice.

Yonekawa T, Malicdan MC, Cho A, Hayashi YK, Nonaka I, Mine T, Yamamoto T, Nishino I, Noguchi S.

Brain. 2014 Oct;137(Pt 10):2670-9. doi: 10.1093/brain/awu210. Epub 2014 Jul 24.

23.

Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s).

Yonekawa T, Nishino I.

J Neurol Neurosurg Psychiatry. 2015 Mar;86(3):280-7. doi: 10.1136/jnnp-2013-307052. Epub 2014 Jun 17. Review.

PMID:
24938411
24.

Direct detection of human herpesvirus 6B by the LAMP method using newly developed dry-reagents.

Yoshikawa T, Matsuo T, Kawamura Y, Ohashi M, Yonekawa T, Kanda H, Notomi T, Ihira M.

J Virol Methods. 2014 Jun;201:65-7. doi: 10.1016/j.jviromet.2014.02.017. Epub 2014 Feb 28.

PMID:
24589515
25.

Anaphylactic transfusion reaction in homozygous haptoglobin deficiency detected by CD203c expression on basophils.

Iwamoto S, Yonekawa T, Azuma E, Fujisawa T, Nagao M, Shimada E, Nakamura R, Teshima R, Ohishi K, Toyoda H, Komada Y.

Pediatr Blood Cancer. 2014 Jul;61(7):1160-1. doi: 10.1002/pbc.24965. Epub 2014 Feb 4. No abstract available.

PMID:
24497482
26.

Interleukin 2 receptor α chain gene polymorphisms and risks of multiple sclerosis and neuromyelitis optica in southern Japanese.

Ainiding G, Kawano Y, Sato S, Isobe N, Matsushita T, Yoshimura S, Yonekawa T, Yamasaki R, Murai H, Kira J; South Japan Multiple Sclerosis Genetics Consortium.

J Neurol Sci. 2014 Feb 15;337(1-2):147-50. doi: 10.1016/j.jns.2013.11.037. Epub 2013 Dec 4.

PMID:
24332945
27.

A nationwide survey of hypertrophic pachymeningitis in Japan.

Yonekawa T, Murai H, Utsuki S, Matsushita T, Masaki K, Isobe N, Yamasaki R, Yoshida M, Kusunoki S, Sakata K, Fujii K, Kira J.

J Neurol Neurosurg Psychiatry. 2014 Jul;85(7):732-9. doi: 10.1136/jnnp-2013-306410. Epub 2013 Nov 22.

PMID:
24273222
28.

Preserved antigen-specific immune response in patients with multiple sclerosis responding to IFNβ-therapy.

Mehling M, Fritz S, Hafner P, Eichin D, Yonekawa T, Klimkait T, Lindberg RL, Kappos L, Hess C.

PLoS One. 2013 Nov 5;8(11):e78532. doi: 10.1371/journal.pone.0078532. eCollection 2013.

29.

Autophagy and cell death.

Yonekawa T, Thorburn A.

Essays Biochem. 2013;55:105-17. doi: 10.1042/bse0550105. Review.

30.

Anti-neurofascin antibody in patients with combined central and peripheral demyelination.

Kawamura N, Yamasaki R, Yonekawa T, Matsushita T, Kusunoki S, Nagayama S, Fukuda Y, Ogata H, Matsuse D, Murai H, Kira J.

Neurology. 2013 Aug 20;81(8):714-22. doi: 10.1212/WNL.0b013e3182a1aa9c. Epub 2013 Jul 24.

PMID:
23884033
31.

Characteristic cerebrospinal fluid cytokine/chemokine profiles in neuromyelitis optica, relapsing remitting or primary progressive multiple sclerosis.

Matsushita T, Tateishi T, Isobe N, Yonekawa T, Yamasaki R, Matsuse D, Murai H, Kira J.

PLoS One. 2013 Apr 18;8(4):e61835. doi: 10.1371/journal.pone.0061835. Print 2013.

32.

Rapidly progressive scoliosis and respiratory deterioration in Ullrich congenital muscular dystrophy.

Yonekawa T, Komaki H, Okada M, Hayashi YK, Nonaka I, Sugai K, Sasaki M, Nishino I.

J Neurol Neurosurg Psychiatry. 2013 Sep;84(9):982-8. doi: 10.1136/jnnp-2012-304710. Epub 2013 Apr 9.

PMID:
23572247
33.

A NOTCH4 missense mutation confers resistance to multiple sclerosis in Japanese.

Huang J, Yoshimura S, Isobe N, Matsushita T, Yonekawa T, Sato S, Yamasaki R, Kira J; South Japan Multiple Sclerosis Genetics Consortium.

Mult Scler. 2013 Nov;19(13):1696-703. doi: 10.1177/1352458513482512. Epub 2013 Apr 2.

PMID:
23549433
34.

Clinical relevance of serum aquaporin-4 antibody levels in neuromyelitis optica.

Isobe N, Yonekawa T, Matsushita T, Masaki K, Yoshimura S, Fichna J, Chen S, Furmaniak J, Smith BR, Kira J.

Neurochem Res. 2013 May;38(5):997-1001. doi: 10.1007/s11064-013-1009-0. Epub 2013 Mar 2.

PMID:
23456674
35.

Congenital hypomyelinating neuropathy attributable to a de novo p.Asp61Asn mutation of the myelin protein zero gene.

Yonekawa T, Komaki H, Saito Y, Takashima H, Sasaki M.

Pediatr Neurol. 2013 Jan;48(1):59-62. doi: 10.1016/j.pediatrneurol.2012.09.011.

PMID:
23290023
36.

Genetic and infectious profiles of Japanese multiple sclerosis patients.

Yoshimura S, Isobe N, Yonekawa T, Matsushita T, Masaki K, Sato S, Kawano Y, Yamamoto K, Kira J; South Japan Multiple Sclerosis Genetics Consortium.

PLoS One. 2012;7(11):e48592. doi: 10.1371/journal.pone.0048592. Epub 2012 Nov 9.

37.

Distinct genetic and infectious profiles in Japanese neuromyelitis optica patients according to anti-aquaporin 4 antibody status.

Yoshimura S, Isobe N, Matsushita T, Yonekawa T, Masaki K, Sato S, Kawano Y, Kira J; South Japan Multiple Sclerosis Genetics Consortium.

J Neurol Neurosurg Psychiatry. 2013 Jan;84(1):29-34. doi: 10.1136/jnnp-2012-302925. Epub 2012 Oct 4.

PMID:
23038741
38.

[Migraine with aura and recurrent vertigo attacks in a patient with hereditary hemorrhagic telangiectasia].

Yonekawa T, Doi H, Tateishi T, Tanaka K, Iura T, Ohyagi Y, Kira J.

Rinsho Shinkeigaku. 2012;52(7):499-502. Japanese.

PMID:
22849993
39.

Quantitative assays for anti-aquaporin-4 antibody with subclass analysis in neuromyelitis optica.

Isobe N, Yonekawa T, Matsushita T, Kawano Y, Masaki K, Yoshimura S, Fichna J, Chen S, Furmaniak J, Smith BR, Kira J.

Mult Scler. 2012 Nov;18(11):1541-51. doi: 10.1177/1352458512443917. Epub 2012 Apr 23.

PMID:
22526930
40.

Peripheral nerve abnormalities in pediatric patients with spinal muscular atrophy.

Yonekawa T, Komaki H, Saito Y, Sugai K, Sasaki M.

Brain Dev. 2013 Feb;35(2):165-71. doi: 10.1016/j.braindev.2012.03.009. Epub 2012 Apr 17.

PMID:
22512990
41.

Extensive loss of connexins in Baló's disease: evidence for an auto-antibody-independent astrocytopathy via impaired astrocyte-oligodendrocyte/myelin interaction.

Masaki K, Suzuki SO, Matsushita T, Yonekawa T, Matsuoka T, Isobe N, Motomura K, Wu XM, Tabira T, Iwaki T, Kira J.

Acta Neuropathol. 2012 Jun;123(6):887-900. doi: 10.1007/s00401-012-0972-x. Epub 2012 Mar 22.

PMID:
22438105
42.

First diagnostic criteria for atopic myelitis with special reference to discrimination from myelitis-onset multiple sclerosis.

Isobe N, Kanamori Y, Yonekawa T, Matsushita T, Shigeto H, Kawamura N, Kira J.

J Neurol Sci. 2012 May 15;316(1-2):30-5. doi: 10.1016/j.jns.2012.02.007. Epub 2012 Feb 25.

PMID:
22364869
43.

PinX1 localizes to telomeres and stabilizes TRF1 at mitosis.

Yonekawa T, Yang S, Counter CM.

Mol Cell Biol. 2012 Apr;32(8):1387-95. doi: 10.1128/MCB.05641-11. Epub 2012 Feb 13.

44.

Comparison of clinical, immunological and neuroimaging features between anti-aquaporin-4 antibody-positive and antibody-negative Sjogren's syndrome patients with central nervous system manifestations.

Estiasari R, Matsushita T, Masaki K, Akiyama T, Yonekawa T, Isobe N, Kira J.

Mult Scler. 2012 Jun;18(6):807-16. doi: 10.1177/1352458511431727. Epub 2012 Jan 30.

PMID:
22291033
45.

[Astrocytopathy in neuromyelitis optica, multiple sclerosis and Baló's disease].

Matsushita T, Masaki K, Suzuki S, Matsuoka T, Yonekawa T, Wu XM, Tabira T, Iwaki T, Kira J.

Rinsho Shinkeigaku. 2011 Nov;51(11):898-900. Japanese.

PMID:
22277409
46.

Effect of corpus callosotomy on attention deficit and behavioral problems in pediatric patients with intractable epilepsy.

Yonekawa T, Nakagawa E, Takeshita E, Inoue Y, Inagaki M, Kaga M, Sugai K, Sasaki M, Kaido T, Takahashi A, Otsuki T.

Epilepsy Behav. 2011 Dec;22(4):697-704. doi: 10.1016/j.yebeh.2011.08.027. Epub 2011 Oct 5.

PMID:
21978470
47.

Interleukin-7 receptor alpha gene polymorphism influences multiple sclerosis risk in Asians.

Fang L, Isobe N, Yoshimura S, Yonekawa T, Matsushita T, Masaki K, Doi H, Ochi K, Miyamoto K, Kawano Y, Kira J; South Japan Multiple Sclerosis Genetics Consortium.

Neurology. 2011 Jun 14;76(24):2125-7. doi: 10.1212/WNL.0b013e31821f466c. No abstract available.

PMID:
21670443
48.

Wall-eyed bilateral internuclear ophthalmoplegia (WEBINO) syndrome in a patient with neuromyelitis optica spectrum disorder and anti-aquaporin-4 antibody.

Shinoda K, Matsushita T, Furuta K, Isobe N, Yonekawa T, Ohyagi Y, Kira J.

Mult Scler. 2011 Jul;17(7):885-7. doi: 10.1177/1352458510391690. Epub 2011 Feb 7.

PMID:
21300735
49.

Three-dimensional echocardiographic imaging of a giant eustachian valve in an infant with reversed cyanosis.

Yonekawa T, Mitani Y, Ohashi H.

Pediatr Cardiol. 2010 Oct;31(7):1114-5. doi: 10.1007/s00246-010-9775-9. Epub 2010 Aug 14. No abstract available.

PMID:
20711569
50.

Augmented startle responses in opsoclonus-myoclonus syndrome.

Yonekawa T, Saito Y, Sakuma H, Sugai K, Shimizu Y, Inagaki M, Sasaki M.

Brain Dev. 2011 Apr;33(4):335-8. doi: 10.1016/j.braindev.2010.06.005. Epub 2010 Jun 29.

PMID:
20591595

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