Kurashige T - Search Results

1

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.

Kume K, Morino H, Miyamoto R, Matsuda Y, Ohsawa R, Kanaya Y, Tada Y, Kurashige T, Kawakami H. Kume K, et al. Among authors: kurashige t. BMC Med Genet. 2020 Mar 31;21(1):68. doi: 10.1186/s12881-020-01002-4. BMC Med Genet. 2020. PMID: 32234020 Free PMC article.

2

Detecting gene mutations in Japanese Alzheimer's patients by semiconductor sequencing.

Yagi R, Miyamoto R, Morino H, Izumi Y, Kuramochi M, Kurashige T, Maruyama H, Mizuno N, Kurihara H, Kawakami H. Yagi R, et al. Among authors: kurashige t. Neurobiol Aging. 2014 Jul;35(7):1780.e1-5. doi: 10.1016/j.neurobiolaging.2014.01.023. Epub 2014 Jan 25. Neurobiol Aging. 2014. PMID: 24559647

3

Multicenter Study of Intravenous Recombinant Tissue Plasminogen Activator Infusion around Hiroshima, Japan: The Hiroshima Acute Stroke Retrospective and Prospective Registry Study.

Aoki S, Hosomi N, Sueda Y, Kono T, Takamatsu K, Ohyama H, Torii T, Kitamura T, Nomura E, Noda K, Ohtsuki T, Matsumoto M; HARP Registry Study Group. Aoki S, et al. J Stroke Cerebrovasc Dis. 2015 Dec;24(12):2747-53. doi: 10.1016/j.jstrokecerebrovasdis.2015.08.005. Epub 2015 Sep 7. J Stroke Cerebrovasc Dis. 2015. PMID: 26360972

4

Prevalences of Peripheral Arterial Disease Diagnosed by Computed Tomography Angiography in Patients with Acute Ischemic Stroke.

Naito H, Naka H, Kobayashi M, Kanaya Y, Naito K, Kurashige T, Tokinobu H, Matsumoto M. Naito H, et al. Among authors: kurashige t. J Stroke Cerebrovasc Dis. 2016 May;25(5):1128-1134. doi: 10.1016/j.jstrokecerebrovasdis.2016.01.029. Epub 2016 Feb 22. J Stroke Cerebrovasc Dis. 2016. PMID: 26915602

5

Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosis.

Izumi Y, Morino H, Miyamoto R, Matsuda Y, Ohsawa R, Kurashige T, Shimatani Y, Kaji R, Kawakami H. Izumi Y, et al. Among authors: kurashige t. Geriatr Gerontol Int. 2018 Oct;18(10):1519-1520. doi: 10.1111/ggi.13506. Geriatr Gerontol Int. 2018. PMID: 30311446 No abstract available.

6

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8.

Kume K, Morino H, Komure O, Matsuda Y, Ohsawa R, Kurashige T, Kanaya Y, Tada Y, Kawakami H. Kume K, et al. Among authors: kurashige t. J Neurol Sci. 2019 Jul 15;402:118-120. doi: 10.1016/j.jns.2019.05.001. Epub 2019 May 9. J Neurol Sci. 2019. PMID: 31129264 No abstract available.

7

Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation.

Kurashige T, Morino H, Matsuda Y, Mukai T, Murao T, Toko M, Kume K, Ohsawa R, Torii T, Tokinobu H, Maruyama H, Kawakami H. Kurashige T, et al. J Neurol Neurosurg Psychiatry. 2020 Feb;91(2):220-222. doi: 10.1136/jnnp-2019-321279. Epub 2019 Aug 20. J Neurol Neurosurg Psychiatry. 2020. PMID: 31431468 No abstract available.

8

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.

Tada Y, Kume K, Matsuda Y, Kurashige T, Kanaya Y, Ohsawa R, Morino H, Tabu H, Kaneko S, Suenaga T, Kakizuka A, Kawakami H. Tada Y, et al. Among authors: kurashige t. J Hum Genet. 2020 Apr;65(4):363-369. doi: 10.1038/s10038-019-0717-y. Epub 2020 Jan 7. J Hum Genet. 2020. PMID: 31907387 Clinical Trial.

9

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.

Matsuda Y, Morino H, Miyamoto R, Kurashige T, Kume K, Mizuno N, Kanaya Y, Tada Y, Ohsawa R, Yokota K, Shimozawa N, Maruyama H, Kawakami H. Matsuda Y, et al. Among authors: kurashige t. Neurol Genet. 2020 Jan 16;6(1):e396. doi: 10.1212/NXG.0000000000000396. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042923 Free PMC article.

10

The first Japanese case of primary familial brain calcification caused by an MYORG variant.

Kume K, Takata T, Morino H, Matsuda Y, Ohsawa R, Tada Y, Kurashige T, Kawakami H. Kume K, et al. Among authors: kurashige t. J Hum Genet. 2020 Oct;65(10):917-920. doi: 10.1038/s10038-020-0779-x. Epub 2020 May 25. J Hum Genet. 2020. PMID: 32451491

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