Moteki Y - Search Results

1

Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.

Moteki Y, Onda H, Kasuya H, Yoneyama T, Okada Y, Hirota K, Mukawa M, Nariai T, Mitani S, Akagawa H. Moteki Y, et al. J Am Heart Assoc. 2015 May 11;4(5):e001862. doi: 10.1161/JAHA.115.001862. J Am Heart Assoc. 2015. PMID: 25964206 Free PMC article.

2

Effectiveness of the Combined Use of Distal Filter Protection Device and Mo.Ma Ultra: Technical Note.

Moteki Y, Niimi Y, Sato S, Inoue T, Shima S, Okada Y. Moteki Y, et al. J Stroke Cerebrovasc Dis. 2016 Nov;25(11):2627-2631. doi: 10.1016/j.jstrokecerebrovasdis.2016.07.003. Epub 2016 Jul 28. J Stroke Cerebrovasc Dis. 2016. PMID: 27476338

3

The Availability of a Tin-Alloyed Omnidirectional Retractor-Supporting Ring for Ventriculoperitoneal Shunt Laparotomy.

Moteki Y, Okada Y, Inoue T, Sato S, Kuwamoto K, Shima S, Niimi Y. Moteki Y, et al. World Neurosurg. 2018 Jan;109:110-114. doi: 10.1016/j.wneu.2017.09.085. Epub 2017 Sep 21. World Neurosurg. 2018. PMID: 28943418

4

[Supratentorial Meningeal Melanoma with Nevus of Ota:A Case Report].

Shima S, Sato S, Moteki Y, Inoue T, Suzuki K, Niimi Y, Okada Y. Shima S, et al. Among authors: moteki y. No Shinkei Geka. 2018 Feb;46(2):139-145. doi: 10.11477/mf.1436203690. No Shinkei Geka. 2018. PMID: 29449519 Japanese.

5

Ruptured Vertebral Artery Dissecting Aneurysm as a Risk Factor for Ocular Symptoms Accompanied with Subarachnoid Hemorrhage.

Moteki Y, Niimi Y, Okada Y, Kawamata T. Moteki Y, et al. World Neurosurg. 2018 Aug;116:e505-e512. doi: 10.1016/j.wneu.2018.05.021. Epub 2018 May 29. World Neurosurg. 2018. PMID: 29758373

6

Genotype-Phenotype Correlation in Long-Term Cohort of Japanese Patients with Moyamoya Disease.

Nomura S, Yamaguchi K, Akagawa H, Kawashima A, Moteki Y, Ishikawa T, Aihara Y, Saito T, Okada Y, Kawamata T. Nomura S, et al. Among authors: moteki y. Cerebrovasc Dis. 2019;47(3-4):105-111. doi: 10.1159/000499699. Epub 2019 Apr 4. Cerebrovasc Dis. 2019. PMID: 30947170

7

Novel RASA1 mutations in Japanese pedigrees with capillary malformation-arteriovenous malformation.

Moteki Y, Akagawa H, Niimi Y, Okada Y, Kawamata T. Moteki Y, et al. Brain Dev. 2019 Oct;41(9):812-816. doi: 10.1016/j.braindev.2019.06.003. Epub 2019 Jun 20. Brain Dev. 2019. PMID: 31230861

8

Prognostic Significance of Hyponatremia in Acute Stroke: A Systematic Review and Meta-Analysis.

Shima S, Niimi Y, Moteki Y, Takahashi O, Sato S, Inoue T, Okada Y. Shima S, et al. Among authors: moteki y. Cerebrovasc Dis. 2020;49(5):531-539. doi: 10.1159/000510751. Epub 2020 Oct 5. Cerebrovasc Dis. 2020. PMID: 33017822

9

Subclavian Artery-Carotid Artery Bypass for Subclavian Artery or Common Carotid Artery Severe Stenosis or Occlusion.

Yamaguchi K, Funatsu T, Moteki Y, Nonaka T, Niwa A, Imanaka K, Kim K, Ishikawa T, Mochizuki T, Okada Y, Kawamata T. Yamaguchi K, et al. Among authors: moteki y. Neurol Med Chir (Tokyo). 2023 Jun 15;63(6):221-227. doi: 10.2176/jns-nmc.2022-0307. Epub 2023 Mar 31. Neurol Med Chir (Tokyo). 2023. PMID: 37005246 Free PMC article.

10

Difference in Clinical Phenotype, Mutation Position, and Structural Change of RNF213 Rare Variants Between Pediatric and Adult Japanese Patients with Moyamoya Disease.

Nomura S, Akagawa H, Yamaguchi K, Azuma K, Nakamura A, Fukui A, Matsuzawa F, Aihara Y, Ishikawa T, Moteki Y, Chiba K, Hashimoto K, Morita S, Ishiguro T, Okada Y, Vetiska S, Andrade-Barazarte H, Radovanovic I, Kawashima A, Kawamata T. Nomura S, et al. Among authors: moteki y. Transl Stroke Res. 2024 Dec;15(6):1142-1153. doi: 10.1007/s12975-023-01194-w. Epub 2023 Sep 28. Transl Stroke Res. 2024. PMID: 37768541

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