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Items: 1 to 50 of 183

1.

Previous Helicobacter pylori infection-induced atrophic gastritis: A distinct disease entity in an understudied population without a history of eradication.

Kishikawa H, Ojiro K, Nakamura K, Katayama T, Arahata K, Takarabe S, Miura S, Kanai T, Nishida J.

Helicobacter. 2019 Nov 3:e12669. doi: 10.1111/hel.12669. [Epub ahead of print] Review.

PMID:
31680399
2.

Skill-up study of systemic endoscopic examination technique using narrow band imaging of the head and neck region of patients with esophageal squamous cell carcinoma: Prospective multicenter study.

Okamoto N, Morimoto H, Yamamoto Y, Kanda K, Nankinzan R, Kasamatsu S, Yoshimura S, Kan M, Nakano A, Hosaka S, Watanabe Y, Arahata K, Toyama Y, Okamura A, Yamaguchi T, Yano T.

Dig Endosc. 2019 Nov;31(6):653-661. doi: 10.1111/den.13445. Epub 2019 Jun 20.

PMID:
31120161
3.

Prepulse inhibition in Drosophila melanogaster larvae.

Matsumoto Y, Shimizu K, Arahata K, Suzuki M, Shimizu A, Takei K, Yamauchi J, Hakeda-Suzuki S, Suzuki T, Morimoto T.

Biol Open. 2018 Sep 27;7(9). pii: bio034710. doi: 10.1242/bio.034710.

4.

A Case of Polymicrobial Bacteremia in a Patient Undergoing Chemotherapy.

Arahata K, Yamaguchi R, Terashima T.

Case Rep Infect Dis. 2018 Jan 15;2018:4165960. doi: 10.1155/2018/4165960. eCollection 2018.

5.

Cutoff Pepsinogen Level for Predicting Unintendedly Eradicated Cases of Helicobacter pylori Infection in Subjects with Seemingly Normal Pepsinogen Levels.

Kishikawa H, Kimura K, Ito A, Arahata K, Takarabe S, Kaida S, Miyauchi J, Miura S, Kanai T, Nishida J.

Digestion. 2017;95(3):229-236. doi: 10.1159/000469705. Epub 2017 Mar 30.

PMID:
28355604
6.

Correction: Association between Increased Gastric Juice Acidity and Sliding Hiatal Hernia Development in Humans.

Kishikawa H, Kimura K, Ito A, Arahata K, Takarabe S, Kaida S, Kanai T, Miura S, Nishida J.

PLoS One. 2017 Feb 13;12(2):e0172375. doi: 10.1371/journal.pone.0172375. eCollection 2017.

7.

Association between Increased Gastric Juice Acidity and Sliding Hiatal Hernia Development in Humans.

Kishikawa H, Kimura K, Ito A, Arahata K, Takarabe S, Kaida S, Kanai T, Miura S, Nishida J.

PLoS One. 2017 Jan 20;12(1):e0170416. doi: 10.1371/journal.pone.0170416. eCollection 2017. Erratum in: PLoS One. 2017 Feb 13;12 (2):e0172375.

8.

Two cases of cystic artery pseudoaneurysm rupture due to acute cholecystitis with gallstone impaction in the neck.

Kaida S, Arahata K, Itou A, Takarabe S, Kimura K, Kishikawa H, Nishida J, Fujiyama Y, Takigawa Y, Matsui J.

Nihon Shokakibyo Gakkai Zasshi. 2016 Sep;113(9):1572-81. doi: 10.11405/nisshoshi.113.1572. Review. Japanese.

PMID:
27593367
9.

Predictors of Gastric Neoplasia in Cases Negative for Helicobacter pylori Antibody and with Normal Pepsinogen.

Kishikawa H, Kimura K, Ito A, Arahata K, Takarabe S, Kaida S, Miyauchi J, Miura S, Nishida J.

Anticancer Res. 2015 Dec;35(12):6765-71. Erratum in: Anticancer Res. 2016 Jan;36(1):477.

PMID:
26637894
10.

"Circular reddish lesions": a possibly characteristic endoscopic finding in Henoch-Schönlein purpura.

Kishikawa H, Nishida J, Takarabe S, Arahata K, Ito A, Miyoshi J, Kaida S, Hibi T.

Endoscopy. 2013;45 Suppl 2 UCTN:E33-4. doi: 10.1055/s-0032-1325886. Epub 2013 Mar 22. No abstract available.

PMID:
23526504
11.

Video capsule endoscopy findings in Ehlers-Danlos syndrome with recurrent gastrointestinal bleeding.

Kishikawa H, Nishida J, Takarabe S, Arahata K, Ito A, Miyoshi J, Kaida S, Hibi T.

Endoscopy. 2012;44 Suppl 2 UCTN:E416. doi: 10.1055/s-0032-1325774. Epub 2012 Nov 20. No abstract available.

PMID:
23169043
12.

The efficacy of home-based muscle training for the elderly osteoporotic women: the effects of daily muscle training on quality of life (QoL).

Kanemaru A, Arahata K, Ohta T, Katoh T, Tobimatsu H, Horiuchi T.

Arch Gerontol Geriatr. 2010 Sep-Oct;51(2):169-72. doi: 10.1016/j.archger.2009.10.003. Epub 2009 Nov 7.

PMID:
19897255
13.

Postictal cardiovascular response predicts therapeutic efficacy of electroconvulsive therapy for depression.

Azuma H, Fujita A, Sato K, Arahata K, Otsuki K, Hori M, Mochida Y, Uchida M, Yamada T, Akechi T, Furukawa TA.

Psychiatry Clin Neurosci. 2007 Jun;61(3):290-4.

14.

Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya.

Kaja S, van de Ven RC, van Dijk JG, Verschuuren JJ, Arahata K, Frants RR, Ferrari MD, van den Maagdenberg AM, Plomp JJ.

Eur J Neurosci. 2007 Apr;25(7):2009-20.

PMID:
17439489
15.

Postictal suppression correlates with therapeutic efficacy for depression in bilateral sine and pulse wave electroconvulsive therapy.

Azuma H, Fujita A, Sato K, Arahata K, Otsuki K, Hori M, Mochida Y, Uchida M, Yamada T, Akechi T, Furukawa TA.

Psychiatry Clin Neurosci. 2007 Apr;61(2):168-73.

16.

Regional cerebral blood flow changes in depression after electroconvulsive therapy.

Segawa K, Azuma H, Sato K, Yasuda T, Arahata K, Otsuki K, Tohyama J, Soma T, Iidaka T, Nakaaki S, Furukawa TA.

Psychiatry Res. 2006 Oct 30;147(2-3):135-43. Epub 2006 Jul 11.

PMID:
16837173
17.

Memory, attention, and executive functions before and after sine and pulse wave electroconvulsive therapies for treatment-resistant major depression.

Fujita A, Nakaaki S, Segawa K, Azuma H, Sato K, Arahata K, Otsuki K, Hori M, Mochida Y, Uchida M, Yamada T, Nakamura C, Akechi T, Furukawa TA.

J ECT. 2006 Jun;22(2):107-12.

PMID:
16801825
18.

[Relationship between activity of daily living and motor function in the community-dwelling elderly after hip fracture].

Fujita H, Shiomi T, Arahata K, Ishibashi H.

Nihon Ronen Igakkai Zasshi. 2006 Mar;43(2):241-5. Japanese.

PMID:
16683660
19.

Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rods.

Schröder R, Reimann J, Salmikangas P, Clemen CS, Hayashi YK, Nonaka I, Arahata K, Carpén O.

Neuromuscul Disord. 2003 Aug;13(6):451-5.

PMID:
12899871
20.

Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.

Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y.

Neurology. 2003 Jun 10;60(11):1799-804.

PMID:
12796534
21.

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Noguchi S, Tsukahara T, Fujita M, Kurokawa R, Tachikawa M, Toda T, Tsujimoto A, Arahata K, Nishino I.

Hum Mol Genet. 2003 Mar 15;12(6):595-600.

PMID:
12620965
22.

A comparative gene expression analysis of Emery-Dreifuss muscular dystrophy using a cDNA microarray.

Tsukahara T, Arahata K.

Methods Mol Biol. 2003;217:253-62. No abstract available.

PMID:
12491938
23.

[Recent advances in limb-girdle muscular dystrophy research].

Nonaka I, Minami N, Chae J, Hayashi YK, Nishino I, Arahata K.

Rinsho Shinkeigaku. 2001 Dec;41(12):1194-7. Review. Japanese.

PMID:
12235836
24.

Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients.

Matsumura T, Goto K, Yamanaka G, Lee JH, Zhang C, Hayashi YK, Arahata K.

BMC Neurol. 2002 Aug 20;2:7.

25.

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].

Yamanaka G, Goto K, Hayashi YK, Miyajima T, Hoshika A, Arahata K.

No To Hattatsu. 2002 Jul;34(4):318-24. Japanese.

PMID:
12134683
26.
27.

Increased expression level of the splicing variant of SIP1 in motor neuron diseases.

Aerbajinai W, Ishihara T, Arahata K, Tsukahara T.

Int J Biochem Cell Biol. 2002 Jun;34(6):699-707.

PMID:
11943600
28.

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.

Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y.

Neurology. 2002 Jan 22;58(2):323-5. Erratum in: Neurology 2002 Mar 12;58(5):839. Itoyoma Y [corrected to Itoyama Y].

PMID:
11805270
29.

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.

Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr.

Hum Mol Genet. 2001 Aug 15;10(17):1761-6.

PMID:
11532985
30.

Tongue atrophy in facioscapulohumeral muscular dystrophy.

Yamanaka G, Goto K, Matsumura T, Funakoshi M, Komori T, Hayashi YK, Arahata K.

Neurology. 2001 Aug 28;57(4):733-5.

PMID:
11524495
31.

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy.

Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers SM, Oeltjen J, Brown HE, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn RJ, Urtizberea JA, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann JS, Brown RH Jr.

Neurology. 2001 Jul 24;57(2):271-8.

PMID:
11468312
32.

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K.

Neurology. 2001 Jul 10;57(1):115-21.

PMID:
11445638
33.

The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression.

Kim YJ, Noguchi S, Hayashi YK, Tsukahara T, Shimizu T, Arahata K.

Hum Mol Genet. 2001 May 15;10(11):1129-39.

PMID:
11371506
34.

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy.

Hayashi YK, Tezak Z, Momoi T, Nonaka I, Garcia CA, Hoffman EP, Arahata K.

Neuromuscul Disord. 2001 May;11(4):350-9.

PMID:
11369186
35.

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene.

Nakagawa M, Matsuzaki T, Suehara M, Kanzato N, Takashima H, Higuchi I, Matsumura T, Goto K, Arahata K, Osame M.

J Neurol Sci. 2001 Feb 15;184(1):15-9.

PMID:
11231027
36.

Interaction between emerin and nuclear lamins.

Sakaki M, Koike H, Takahashi N, Sasagawa N, Tomioka S, Arahata K, Ishiura S.

J Biochem. 2001 Feb;129(2):321-7.

37.

[Exercise training improves activities of daily living in elderly patients with congestive heart failure].

Arahata K, Uchiyama S, Fujita H, Osanai T, Narita J, Kokubu E, Nakahara K, Matsushita S, Nishinaga M.

Nihon Ronen Igakkai Zasshi. 2000 Sep;37(9):728-33. Japanese.

38.

Nuclear envelope proteins and associated diseases.

Nagano A, Arahata K.

Curr Opin Neurol. 2000 Oct;13(5):533-9. Review.

PMID:
11073359
39.

Developmental expression of myotonic dystrophy protein kinase in brain and its relevance to clinical phenotype.

Endo A, Motonaga K, Arahata K, Harada K, Yamada T, Takashima S.

Acta Neuropathol. 2000 Nov;100(5):513-20.

PMID:
11045673
40.

Muscular dystrophy.

Arahata K.

Neuropathology. 2000 Sep;20 Suppl:S34-41. Review.

PMID:
11037185
41.

Nuclear accumulation of expanded PABP2 gene product in oculopharyngeal muscular dystrophy.

Uyama E, Tsukahara T, Goto K, Kurano Y, Ogawa M, Kim YJ, Uchino M, Arahata K.

Muscle Nerve. 2000 Oct;23(10):1549-54.

PMID:
11003790
42.

Expression of human GFR alpha-1 (GDNF receptor) at the neuromuscular junction and myelinated nerves.

Hase A, Suzuki H, Arahata K, Akazawa C.

Neurosci Lett. 1999 Jul 2;269(1):55-7.

PMID:
10821644
43.

Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.

Tagawa K, Taya C, Hayashi Y, Nakagawa M, Ono Y, Fukuda R, Karasuyama H, Toyama-Sorimachi N, Katsui Y, Hata S, Ishiura S, Nonaka I, Seyama Y, Arahata K, Yonekawa H, Sorimachi H, Suzuki K.

Hum Mol Genet. 2000 May 22;9(9):1393-402.

PMID:
10814721
44.

[Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy].

Aoki M, Arahata K, Brown RH Jr.

Rinsho Shinkeigaku. 1999 Dec;39(12):1272-5. Japanese.

PMID:
10791095
45.

Emerin, deficiency of which causes Emery-Dreifuss muscular dystrophy, is localized at the inner nuclear membrane.

Yorifuji H, Tadano Y, Tsuchiya Y, Ogawa M, Goto K, Umetani A, Asaka Y, Arahata K.

Neurogenetics. 1997 Sep;1(2):135-40.

PMID:
10732816
46.

[A novel splice-site mutation in the STA gene in a Japanese patient with Emery-Dreifuss muscular dystrophy].

Hasegawa T, Kobayashi K, Arahata K, Itoyama Y.

Rinsho Shinkeigaku. 1999 Nov;39(11):1138-43. Japanese.

PMID:
10689937
47.

Changes in pre-mRNA splicing factors during neural differentiation in P19 embryonal carcinoma cells.

Shinozaki A, Arahata K, Tsukahara T.

Int J Biochem Cell Biol. 1999 Nov;31(11):1279-87.

PMID:
10605820
48.
49.

Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy.

Matsuda C, Aoki M, Hayashi YK, Ho MF, Arahata K, Brown RH Jr.

Neurology. 1999 Sep 22;53(5):1119-22.

PMID:
10496277
50.

Early onset of X-linked Emery-Dreifuss muscular dystrophy in a boy with emerin gene deletion.

Fujimoto S, Ishikawa T, Saito M, Wada Y, Wada I, Arahata K, Nonaka I.

Neuropediatrics. 1999 Jun;30(3):161-3.

PMID:
10480214

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