Hashiguchi A - Search Results

1

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.

Tanabe H, Higuchi Y, Yuan JH, Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, Sunami Y, Kono Y, Ishigaki Y, Yanamoto S, Fukae J, Kida H, Morita M, Tsuji S, Takashima H. Tanabe H, et al. Among authors: hashiguchi a. J Peripher Nerv Syst. 2018 Mar;23(1):40-48. doi: 10.1111/jns.12252. Epub 2018 Feb 14. J Peripher Nerv Syst. 2018. PMID: 29381233 Free PMC article.

2

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: hashiguchi a. Neurogenetics. 2006 Jul;7(3):175-83. doi: 10.1007/s10048-006-0046-0. Epub 2006 Jun 15. Neurogenetics. 2006. PMID: 16779558

3

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases.

Higuchi I, Hashiguchi A, Matsuura E, Higashi K, Shiraishi T, Hirata N, Arimura K, Osame M. Higuchi I, et al. Among authors: hashiguchi a. Neuromuscul Disord. 2007 Mar;17(3):221-6. doi: 10.1016/j.nmd.2006.11.008. Epub 2007 Feb 26. Neuromuscul Disord. 2007. PMID: 17324572

4

[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: hashiguchi a. 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.

5

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

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

6

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: hashiguchi a. Neurogenetics. 2012 Feb;13(1):77-82. doi: 10.1007/s10048-012-0313-1. Epub 2012 Jan 25. Neurogenetics. 2012. PMID: 22271166

7

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: hashiguchi a. 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

8

Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy.

Zhao Z, Hashiguchi A, Hu J, Sakiyama Y, Okamoto Y, Tokunaga S, Zhu L, Shen H, Takashima H. Zhao Z, et al. Among authors: hashiguchi a. Neurology. 2012 May 22;78(21):1644-9. doi: 10.1212/WNL.0b013e3182574f8f. Epub 2012 May 9. Neurology. 2012. PMID: 22573628 Free PMC article.

9

A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease.

Shiga K, Noto Y, Mizuta I, Hashiguchi A, Takashima H, Nakagawa M. Shiga K, et al. Among authors: hashiguchi a. J Peripher Nerv Syst. 2012 Jun;17(2):206-9. doi: 10.1111/j.1529-8027.2012.00403.x. J Peripher Nerv Syst. 2012. PMID: 22734907

10

Late-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation.

Tokunaga S, Hashiguchi A, Yoshimura A, Maeda K, Suzuki T, Haruki H, Nakamura T, Okamoto Y, Takashima H. Tokunaga S, et al. Among authors: hashiguchi a. Neurogenetics. 2012 Nov;13(4):359-65. doi: 10.1007/s10048-012-0338-5. Epub 2012 Aug 1. Neurogenetics. 2012. PMID: 22847150

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