Takashima H - Search Results

1

Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults.

Hidaka M, Higashi E, Uwatoko T, Uwatoko K, Urashima M, Takashima H, Watanabe Y, Kitazono T, Sugimori H. Hidaka M, et al. Among authors: takashima h. Acute Med Surg. 2020 Sep 8;7(1):e565. doi: 10.1002/ams2.565. eCollection 2020 Jan-Dec. Acute Med Surg. 2020. PMID: 32995020 Free PMC article.

2

Aspiration Catheter Reach to Thrombus (ART) Sign in Combined Technique for Mechanical Thrombectomy: Impact for First-Pass Complete Reperfusion.

Mizokami T, Uwatoko T, Matsumoto K, Ooya Y, Hashimoto G, Koguchi M, Iwashita H, Uwatoko K, Takashima H, Sugimori H, Sakata S. Mizokami T, et al. Among authors: takashima h. J Stroke Cerebrovasc Dis. 2019 Oct;28(10):104301. doi: 10.1016/j.jstrokecerebrovasdis.2019.07.017. Epub 2019 Jul 31. J Stroke Cerebrovasc Dis. 2019. PMID: 31375403

3

Blood Pressure Level and Variability During Long-Term Prasugrel or Clopidogrel Medication After Stroke: PRASTRO-I.

Toyoda K, Yamagami H, Kitagawa K, Kitazono T, Nagao T, Minematsu K, Uchiyama S, Tanahashi N, Matsumoto M, Nagata I, Nishikawa M, Nanto S, Shirai T, Abe K, Ikeda Y, Ogawa A; PRASTRO Trial Investigators*. Toyoda K, et al. Stroke. 2021 Apr;52(4):1234-1243. doi: 10.1161/STROKEAHA.120.032824. Epub 2021 Feb 10. Stroke. 2021. PMID: 33563017 Free article. Clinical Trial.

4

[A case of recurrent cerebral vein thrombosis with protein C gene mutation identified].

Sugahara Y, Ono N, Morishita E, Takashima H. Sugahara Y, et al. Among authors: takashima h. Rinsho Shinkeigaku. 2018 Dec 21;58(12):764-766. doi: 10.5692/clinicalneurol.cn-001221. Epub 2018 Nov 29. Rinsho Shinkeigaku. 2018. PMID: 30487363 Japanese.

5

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.

Sakiyama Y, Okamoto Y, Higuchi I, Inamori Y, Sangatsuda Y, Michizono K, Watanabe O, Hatakeyama H, Goto Y, Arimura K, Takashima H. Sakiyama Y, et al. Among authors: takashima h. Acta Neuropathol. 2011 Jun;121(6):775-83. doi: 10.1007/s00401-011-0818-y. Epub 2011 Mar 22. Acta Neuropathol. 2011. PMID: 21424749 Free PMC article.

6

[Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease].

Yamamoto Y, Matsui N, Hiramatsu Y, Miyazaki Y, Nodera H, Izumi Y, Takashima H, Kaji R. Yamamoto Y, et al. Among authors: takashima h. Rinsho Shinkeigaku. 2017 Feb 25;57(2):82-87. doi: 10.5692/clinicalneurol.cn-000976. Epub 2017 Jan 28. Rinsho Shinkeigaku. 2017. PMID: 28132977 Japanese.

7

Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann-Sträussler-Scheinker Disease.

Honda H, Sasaki K, Takashima H, Mori D, Koyama S, Suzuki SO, Iwaki T. Honda H, et al. Among authors: takashima h. J Neuropathol Exp Neurol. 2017 Oct 1;76(10):854-863. doi: 10.1093/jnen/nlx068. J Neuropathol Exp Neurol. 2017. PMID: 28922846

8

Enhancement of the Ivy Sign during an Ischemic Event in Moyamoya Disease.

Hamada Y, Shigehisa A, Kanda Y, Ikeda M, Takaguchi G, Matsuoka H, Takashima H. Hamada Y, et al. Among authors: takashima h. Intern Med. 2023 Feb 15;62(4):617-621. doi: 10.2169/internalmedicine.9326-22. Epub 2022 Jul 29. Intern Med. 2023. PMID: 35908969 Free PMC article.

9

A family of McLeod syndrome, masquerading as chorea-acanthocytosis.

Takashima H, Sakai T, Iwashita H, Matsuda Y, Tanaka K, Oda K, Okubo Y, Reid ME. Takashima H, et al. J Neurol Sci. 1994 Jun;124(1):56-60. doi: 10.1016/0022-510x(94)90010-8. J Neurol Sci. 1994. PMID: 7931422

10

Cerebral infarction associated with accessory middle cerebral arteries: two case reports.

Hiramatsu Y, Wakita M, Matsuoka H, Kasuya J, Hamada R, Takashima H. Hiramatsu Y, et al. Among authors: takashima h. Intern Med. 2014;53(12):1381-4. doi: 10.2169/internalmedicine.53.1760. Epub 2014 Jun 15. Intern Med. 2014. PMID: 24930662 Free article.

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