Hashiguchi A - Search Results

1

Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II.

Shima T, Yamamoto Y, Kanazawa N, Murata KY, Ito H, Kondo T, Yuan J, Hashiguchi A, Takashima H, Furukawa F. Shima T, et al. Among authors: hashiguchi a. J Dermatol. 2018 Nov;45(11):e308-e309. doi: 10.1111/1346-8138.14336. Epub 2018 Apr 27. J Dermatol. 2018. PMID: 29701257 No abstract available.

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

[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.

4

[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.

5

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

6

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

7

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

8

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

9

A family with IVIg-responsive Charcot-Marie-Tooth disease.

Miki Y, Tomiyama M, Haga R, Nishijima H, Suzuki C, Kurihara A, Sugimoto K, Hashiguchi A, Takashima H, Baba M. Miki Y, et al. Among authors: hashiguchi a. J Neurol. 2013 Apr;260(4):1147-51. doi: 10.1007/s00415-012-6782-1. Epub 2012 Dec 12. J Neurol. 2013. PMID: 23232577

10

Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.

Yuan J, Higuchi Y, Nagado T, Nozuma S, Nakamura T, Matsuura E, Hashiguchi A, Sakiyama Y, Yoshimura A, Takashima H. Yuan J, et al. Among authors: hashiguchi a. J Peripher Nerv Syst. 2013 Mar;18(1):89-93. doi: 10.1111/jns5.12012. J Peripher Nerv Syst. 2013. PMID: 23521649

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