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Items: 1 to 50 of 59

1.

Subtyping of Type 1 Diabetes as Classified by Anti-GAD Antibody, IgE Levels, and Tyrosine kinase 2 (TYK2) Promoter Variant in the Japanese.

Mine K, Hirakawa K, Kondo S, Minami M, Okada A, Tsutsu N, Yokogawa Y, Hibio Y, Kojima F, Fujimoto S, Kurisaki H, Anzai K, Yoshikai Y, Nagafuchi S; West Japan Pathogenesis of Diabetes Study Group.

EBioMedicine. 2017 Sep;23:46-51. doi: 10.1016/j.ebiom.2017.08.012. Epub 2017 Aug 12.

2.

TYK2 Promoter Variant and Diabetes Mellitus in the Japanese.

Nagafuchi S, Kamada-Hibio Y, Hirakawa K, Tsutsu N, Minami M, Okada A, Kai K, Teshima M, Moroishi A, Murakami Y, Umeno Y, Yokogawa Y, Kogawa K, Izumi K, Anzai K, Iwakiri R, Hamaguchi K, Sasaki N, Nohara S, Yoshida E, Harada M, Akashi K, Yanase T, Ono J, Okeda T, Fujimoto R, Ihara K, Hara T, Kikuchi Y, Iwase M, Kitazono T, Kojima F, Kono S, Kurisaki H, Kondo S, Katsuta H.

EBioMedicine. 2015 May 9;2(7):744-9. doi: 10.1016/j.ebiom.2015.05.004. eCollection 2015 Jul.

3.

Reduced Tyk2 gene expression in β-cells due to natural mutation determines susceptibility to virus-induced diabetes.

Izumi K, Mine K, Inoue Y, Teshima M, Ogawa S, Kai Y, Kurafuji T, Hirakawa K, Miyakawa D, Ikeda H, Inada A, Hara M, Yamada H, Akashi K, Niho Y, Ina K, Kobayashi T, Yoshikai Y, Anzai K, Yamashita T, Minagawa H, Fujimoto S, Kurisaki H, Shimoda K, Katsuta H, Nagafuchi S.

Nat Commun. 2015 Apr 7;6:6748. doi: 10.1038/ncomms7748.

4.

Neurosyphilis presenting as frontal and mesial temporal encephalitis.

Aizawa H, Yomono H, Kurisaki H.

Intern Med. 2013;52(20):2381-2. No abstract available.

5.

Autoimmune gastro-pancreatitis with anti-protein disulfide isomerase-associated 2 autoantibody in Aire-deficient BALB/cAnN mice.

Kurisaki H, Nagao Y, Nagafuchi S, Mitsuyama M.

PLoS One. 2013 Aug 26;8(8):e73862. doi: 10.1371/journal.pone.0073862. eCollection 2013.

6.

Regulation of human autoimmune regulator (AIRE) gene translation by miR-220b.

Matsuo T, Noguchi Y, Shindo M, Morita Y, Oda Y, Yoshida E, Hamada H, Harada M, Shiokawa Y, Nishida T, Tominaga R, Kikushige Y, Akashi K, Kudoh J, Shimizu N, Tanaka Y, Umemura T, Taniguchi T, Yoshimura A, Kobayashi T, Mitsuyama M, Kurisaki H, Katsuta H, Nagafuchi S.

Gene. 2013 Nov 1;530(1):19-25. doi: 10.1016/j.gene.2013.08.015. Epub 2013 Aug 14.

PMID:
23954874
7.

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease.

Yoshida T, Mizuta I, Saito K, Ohara R, Kurisaki H, Ohnari K, Riku Y, Hayashi Y, Suzuki H, Shii H, Fujiwara Y, Yonezu T, Nagaishi A, Nakagawa M.

J Hum Genet. 2013 Sep;58(9):635-8. doi: 10.1038/jhg.2013.83. Epub 2013 Aug 1.

PMID:
23903069
8.

Spinocerebellar ataxia type 2 is associated with Parkinsonism and Lewy body pathology.

Takao M, Aoyama M, Ishikawa K, Sakiyama Y, Yomono H, Saito Y, Kurisaki H, Mihara B, Murayama S.

BMJ Case Rep. 2011 Apr 1;2011. pii: bcr0120113685. doi: 10.1136/bcr.01.2011.3685.

9.

CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease.

Matsumoto L, Takuma H, Tamaoka A, Kurisaki H, Date H, Tsuji S, Iwata A.

PLoS One. 2010 Nov 24;5(11):e15522. doi: 10.1371/journal.pone.0015522.

10.

[Autopsy case of SCA2 with Parkinsonian phenotype].

Yomono HS, Kurisaki H, Hebisawa A, Sakiyama Y, Saito Y, Murayama S.

Rinsho Shinkeigaku. 2010 Mar;50(3):156-62. Japanese.

PMID:
20235484
11.

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.

Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O.

Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25.

PMID:
18579805
12.

The significance of T cells, B cells, antibodies and macrophages against encephalomyocarditis (EMC)-D virus-induced diabetes in mice.

Kounoue E, Izumi K, Ogawa S, Kondo S, Katsuta H, Akashi T, Niho Y, Harada M, Tamiya S, Kurisaki H, Nagafuchi S.

Arch Virol. 2008;153(7):1223-31. doi: 10.1007/s00705-008-0106-x. Epub 2008 May 24.

PMID:
18500429
13.
14.

[Case of opticospinal multiple sclerosis showing phenotype change to conventional type induced by interferon beta-1b].

Kanzaki M, Yomono H, Ogawa G, Motoyoshi K, Kurisaki H, Kamakura K.

Rinsho Shinkeigaku. 2007 Feb-Mar;47(2-3):100-4. Japanese.

PMID:
17511277
15.

Autoimmune regulator (AIRE) gene is expressed in human activated CD4+ T-cells and regulated by mitogen-activated protein kinase pathway.

Nagafuchi S, Katsuta H, Koyanagi-Katsuta R, Yamasaki S, Inoue Y, Shimoda K, Ikeda Y, Shindo M, Yoshida E, Matsuo T, Ohno Y, Kogawa K, Anzai K, Kurisaki H, Kudoh J, Harada M, Shimizu N.

Microbiol Immunol. 2006;50(12):979-87.

16.

The C-terminal tail of mitochondrial transcription factor a markedly strengthens its general binding to DNA.

Ohgaki K, Kanki T, Fukuoh A, Kurisaki H, Aoki Y, Ikeuchi M, Kim SH, Hamasaki N, Kang D.

J Biochem. 2007 Feb;141(2):201-11. Epub 2006 Dec 13.

PMID:
17167045
17.

[Transcortical sensory aphasia due to extensive infarction of left cerebral hemisphere].

Warabi Y, Bandoh M, Kurisaki H, Nishio S, Hayashi H.

Rinsho Shinkeigaku. 2006 May;46(5):317-21. Japanese.

PMID:
16886797
18.

[Parkinson disease with dementia--responsible locus for dementia].

Murayama S, Saito Y, Ishii K, Mitani K, Kanemaru K, Yamanouchi H, Kurisaki H, Imafuku I.

Rinsho Shinkeigaku. 2004 Nov;44(11):824-6. Review. Japanese.

PMID:
15651303
19.

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S.

Neurology. 2004 Feb 24;62(4):648-51.

PMID:
14981189
20.

[An autopsy case of multiple system atrophy with a heteroallelic ceruloplasmin gene mutation].

Yomono H, Kurisaki H, Murayama S, Hebisawa A, Miyajima H, Takahashi Y.

Rinsho Shinkeigaku. 2003 Jul;43(7):398-402. Japanese.

PMID:
14582365
21.

Pressure-induced superconductor-insulator transition in the spinel compound CuRh2S4.

Ito M, Hori J, Kurisaki H, Okada H, Perez Kuroki AJ, Ogita N, Udagawa M, Fujii H, Nakamura F, Fujita T, Suzuki T.

Phys Rev Lett. 2003 Aug 15;91(7):077001. Epub 2003 Aug 12.

PMID:
12935045
22.

[Multiple system atrophy with a-/hypo-ceruloplasminemia: distribution of iron in brains of 2 autopsy cases].

Kurisaki H, Yomono H, Murayama S, Hebisawa A.

Rinsho Shinkeigaku. 2002 Apr;42(4):293-8. Japanese.

PMID:
12561083
23.

Decrease of neurons in the medullary arcuate nucleus in myotonic dystrophy.

Ono S, Takahashi K, Kanda F, Jinnai K, Fukuoka Y, Mitake S, Inagaki T, Kurisaki H, Nagao K, Shimizu N.

Acta Neuropathol. 2001 Jul;102(1):89-93.

PMID:
11547956
24.
25.

[Prognosis of multiple system atrophy--survival time with or without tracheostomy].

Kurisaki H.

Rinsho Shinkeigaku. 1999 May;39(5):503-7. Japanese.

PMID:
10424139
26.

Abnormal dentatorubral-pallidoluysian atrophy (DRPLA) protein complex is pathologically ubiquitinated in DRPLA brains.

Yazawa I, Nakase H, Kurisaki H.

Biochem Biophys Res Commun. 1999 Jun 24;260(1):133-8.

PMID:
10381356
27.

Loss of catecholaminergic neurons in the medullary reticular formation in myotonic dystrophy.

Ono S, Takahashi K, Jinnai K, Kanda F, Fukuoka Y, Kurisaki H, Mitake S, Inagaki T, Yamano T, Shimizu N, Nagao K.

Neurology. 1998 Oct;51(4):1121-4.

PMID:
9781540
28.

Reversible memory disturbance and intelligence impairment induced by long-term anticholinergic therapy.

Nishiyama K, Sugishita M, Kurisaki H, Sakuta M.

Intern Med. 1998 Jun;37(6):514-8.

29.

Loss of serotonin-containing neurons in the raphe of patients with myotonic dystrophy: a quantitative immunohistochemical study and relation to hypersomnia.

Ono S, Takahashi K, Jinnai K, Kanda F, Fukuoka Y, Kurisaki H, Mitake S, Inagaki T, Yamano T, Nagao K.

Neurology. 1998 Feb;50(2):535-8.

PMID:
9484393
30.

Intracytoplasmic inclusion bodies of the substantia nigra in myotonic dystrophy. Immunohistochemical observations.

Ono S, Takahashi K, Fukuoka Y, Jinnai K, Kanda F, Kurisaki H, Mitake S, Inagaki T, Nagao K.

J Neurol Sci. 1997 May 29;148(2):193-8.

PMID:
9129116
32.

Expression of dentatorubral-pallidoluysian atrophy (DRPLA) proteins in patients.

Yazawa I, Nukina N, Goto J, Kurisaki H, Hebisawa A, Kanazawa I.

Neurosci Lett. 1997 Mar 28;225(1):53-6.

PMID:
9143016
33.

Immunohistochemical study of intracytoplasmic inclusion bodies of the thalamus in myotonic dystrophy.

Ono S, Takahashi K, Kanda F, Fukuoka Y, Jinnai K, Kurisaki H, Mitake S, Inagaki T, Nagao K.

J Neurol Sci. 1996 Sep 1;140(1-2):96-100.

PMID:
8866433
34.

Neuronal loss in the medullary reticular formation in myotonic dystrophy: a clinicopathological study.

Ono S, Kanda F, Takahashi K, Fukuoka Y, Jinnai K, Kurisaki H, Mitake S, Inagaki T, Nagao K.

Neurology. 1996 Jan;46(1):228-31.

PMID:
8559381
35.

A new familial disorder presenting with amyotrophic lateral sclerosis-like manifestation: a clinicopathological study.

Ono S, Inoue K, Kurisaki H, Okiyama R, Shimizu J, Nagao K.

J Neurol Sci. 1995 Dec;134(1-2):160-6.

PMID:
8747860
36.

Myotonic dystrophy with alveolar hypoventilation and hypersomnia: a clinicopathological study.

Ono S, Kurisaki H, Sakuma A, Nagao K.

J Neurol Sci. 1995 Feb;128(2):225-31.

PMID:
7738599
37.

Neuronal cell loss in the dorsal raphe nucleus and the superior central nucleus in myotonic dystrophy: a clinicopathological correlation.

Ono S, Kanda F, Takahashi K, Fukuoka Y, Jinnai K, Kurisaki H, Mitake S, Inagaki T, Nagao K.

Acta Neuropathol. 1995;89(2):122-5.

PMID:
7732784
38.

Transient partial verbal amnesia.

Nishiyama K, Kurisaki H, Bandoh M, Ishikawa T, Sugishita M.

J Neurol Neurosurg Psychiatry. 1993 Nov;56(11):1234-5. No abstract available.

39.
40.

[A case of rabbit syndrome--its unique pharmacological feature].

Nishiyama K, Masuda N, Kurisaki H.

Rinsho Shinkeigaku. 1993 Jun;33(6):663-5. Japanese.

PMID:
8104749
41.

Carcinomatous neuropathy associated with hepatic cell carcinoma: an autopsy case report.

Nishiyama K, Kurisaki H, Masuda N, Kusunoki S, Takatsu M.

Neuromuscul Disord. 1993 May;3(3):227-9.

PMID:
8400864
42.

[Natural type interferon-alpha (Namalwa) therapy for multiple myeloma complicated by hemolytic anemia].

Sone Y, Kawano F, Nishimura Y, Kurisaki H, Tsukamoto A, Kiyokawa T, Sanada I, Shido T.

Rinsho Ketsueki. 1993 May;34(5):670-2. Japanese.

PMID:
8315840
43.
44.

[Isospora belli infection in a patient with adult T-cell leukemia].

Kawano F, Nishida K, Kurisaki H, Tsukamoto A, Satoh M, Sanada I, Shido T, Obata S, Kimura K, Sasaki Y, et al.

Rinsho Ketsueki. 1992 May;33(5):683-7. Review. Japanese.

PMID:
1630021
45.

Japanese crossed Wernicke's aphasia.

Sakurai Y, Kurisaki H, Takeda K, Iwata M, Bandoh M, Watanabe T, Momose T.

Neurology. 1992 Jan;42(1):144-8. Erratum in: Neurology 1992 Mar;42(3 Pt 1):668.

PMID:
1734296
46.

[Chronic dementia in Parkinson disease treated by long-term administration of anticholinergic drug--evaluation of neuropsychological test, PET, and SPECT].

Nishiyama K, Mizuno T, Sakuta M, Kurisaki H, Momose T.

Rinsho Shinkeigaku. 1991 Jun;31(6):625-31. Japanese.

PMID:
1934777
47.

["AB-Triple V" therapy of relapsed or refractory acute myelogenous leukemia].

Asou N, Suzushima H, Hamasaki N, Goto J, Hidaka M, Akagi K, Kurisaki H, Sawatari T, Kawano F, Takatsuki K.

Rinsho Ketsueki. 1989 Feb;30(2):169-74. Japanese.

PMID:
2746873
48.

An unusual neurological disorder with abnormal copper metabolism.

Ono S, Kurisaki H.

J Neurol. 1988 Sep;235(7):397-9. Review.

PMID:
3065463
49.

[Spinal muscular atrophy with features of myasthenia gravis and Eaton-Lambert syndrome. A case report].

Ono S, Kurisaki H.

Rinsho Shinkeigaku. 1988 May;28(5):497-500. Japanese. No abstract available.

PMID:
2850884
50.

[A disorder with low serum copper level, dementia, dysarthria, gait disturbance and involuntary movements].

Ono S, Kurisaki H, Kamakura K.

Rinsho Shinkeigaku. 1988 Apr;28(4):433-6. Japanese. No abstract available.

PMID:
3214981

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