Takashima H - Search Results

1

[A case of motor and sensory polyneuropathy and respiratory failure with novel heterozygous mutation of the senataxin gene].

Kitao R, Honma Y, Hashiguchi A, Mizoguchi K, Takashima H, Komori T. Kitao R, et al. Among authors: takashima h. Rinsho Shinkeigaku. 2020 Jul 31;60(7):466-472. doi: 10.5692/clinicalneurol.60.cn-001415. Epub 2020 Jun 13. Rinsho Shinkeigaku. 2020. PMID: 32536663 Japanese.

2

[Molecular genetics of inherited neuropathies].

Takashima H. Takashima H. Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Rinsho Shinkeigaku. 2006. PMID: 16541790 Review. Japanese.

3

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.

Okamoto Y, Takashima H, Higuchi I, Matsuyama W, Suehara M, Nishihira Y, Hashiguchi A, Hirano R, Ng AR, Nakagawa M, Izumo S, Osame M, Arimura K. Okamoto Y, et al. Among authors: takashima h. Neurogenetics. 2006 Jul;7(3):175-83. doi: 10.1007/s10048-006-0046-0. Epub 2006 Jun 15. Neurogenetics. 2006. PMID: 16779558

4

[Molecular genetics of inherited neuropathies].

Takashima H. Takashima H. Rinsho Shinkeigaku. 2006 Nov;46(11):760-7. Rinsho Shinkeigaku. 2006. PMID: 17432174 Review. Japanese.

5

[Mitochondrial encephalomyopathy with elderly onset of psychiatric disorder].

Moriyama H, Ichiki M, Arime T, Hashiguchi A, Kanda N, Ikeda K, Takashima H, Higuchi I, Osame M, Arimura K. Moriyama H, et al. Among authors: takashima h. Nihon Naika Gakkai Zasshi. 2007 Nov 10;96(11):2536-8. doi: 10.2169/naika.96.2536. Nihon Naika Gakkai Zasshi. 2007. PMID: 18069310 Japanese. No abstract available.

6

[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].

Sakiyama Y, Michizono K, Tomari S, Watanabe O, Nakahara K, Takashima H. Sakiyama Y, et al. Among authors: takashima h. Rinsho Shinkeigaku. 2011 Jan;51(1):38-42. doi: 10.5692/clinicalneurol.51.38. Rinsho Shinkeigaku. 2011. PMID: 21387699 Japanese.

7

[Hereditary neuropathy: variety of disease-causing genes and progress of molecular genetic diagnosis].

Hashiguchi A, Takashima H. Hashiguchi A, et al. Among authors: takashima h. Brain Nerve. 2011 Jun;63(6):539-48. Brain Nerve. 2011. PMID: 21613657 Review. Japanese.

8

[Neurological disorders and RNA].

Goto J, Takashima H. Goto J, et al. Among authors: takashima h. Rinsho Shinkeigaku. 2010 Nov;50(11):977. Rinsho Shinkeigaku. 2010. PMID: 21921532 Japanese. No abstract available.

9

Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutation.

Nakamura T, Hashiguchi A, Suzuki S, Uozumi K, Tokunaga S, Takashima H. Nakamura T, et al. Among authors: takashima h. Neurogenetics. 2012 Feb;13(1):77-82. doi: 10.1007/s10048-012-0313-1. Epub 2012 Jan 25. Neurogenetics. 2012. PMID: 22271166

10

Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study.

Inamori Y, Higuchi I, Inoue T, Sakiyama Y, Hashiguchi A, Higashi K, Shiraishi T, Okubo R, Arimura K, Mitsuyama Y, Takashima H. Inamori Y, et al. Among authors: takashima h. Neuromuscul Disord. 2012 Aug;22(8):747-54. doi: 10.1016/j.nmd.2012.03.011. Epub 2012 May 4. Neuromuscul Disord. 2012. PMID: 22560514

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