Morino H - Search Results

1

Complete nanopore repeat sequencing of SCA27B (GAA-FGF14 ataxia) in Japanese.

Miyatake S, Doi H, Yaguchi H, Koshimizu E, Kihara N, Matsubara T, Mori Y, Kunieda K, Shimizu Y, Toyota T, Shirai S, Matsushima M, Okubo M, Wada T, Kunii M, Johkura K, Miyamoto R, Osaki Y, Miyama T, Satoh M, Fujita A, Uchiyama Y, Tsuchida N, Misawa K, Hamanaka K, Hamanoue H, Mizuguchi T, Morino H, Izumi Y, Shimohata T, Yoshida K, Adachi H, Tanaka F, Yabe I, Matsumoto N. Miyatake S, et al. Among authors: morino h. J Neurol Neurosurg Psychiatry. 2024 Nov 18;95(12):1187-1195. doi: 10.1136/jnnp-2024-333541. J Neurol Neurosurg Psychiatry. 2024. PMID: 38816190

2

Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer's disease.

Maruyama H, Izumi Y, Oda M, Torii T, Morino H, Toji H, Sasaki K, Terasawa H, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: morino h. Neurology. 2001 Jul 24;57(2):337-9. doi: 10.1212/wnl.57.2.337. Neurology. 2001. PMID: 11468325

3

Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.

Nishimura M, Kawakami H, Komure O, Maruyama H, Morino H, Izumi Y, Nakamura S, Kaji R, Kuno S. Nishimura M, et al. Among authors: morino h. Mov Disord. 2002 Jul;17(4):808-11. doi: 10.1002/mds.10124. Mov Disord. 2002. PMID: 12210881

4

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.

Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: morino h. Am J Hum Genet. 2003 Mar;72(3):704-9. doi: 10.1086/367775. Epub 2003 Jan 21. Am J Hum Genet. 2003. PMID: 12545428 Free PMC article.

5

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H. Oda M, et al. Among authors: morino h. Arch Neurol. 2004 Feb;61(2):209-12. doi: 10.1001/archneur.61.2.209. Arch Neurol. 2004. PMID: 14967767

6

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in western Japan.

Terasawa H, Oda M, Morino H, Miyachi T, Izumi Y, Maruyama H, Matsumoto M, Kawakami H. Terasawa H, et al. Among authors: morino h. Neurosci Lett. 2004 Mar 25;358(2):107-10. doi: 10.1016/j.neulet.2004.01.007. Neurosci Lett. 2004. PMID: 15026160

7

The clinical characteristics of spinocerebellar ataxia 36: a study of 2121 Japanese ataxia patients.

Sugihara K, Maruyama H, Morino H, Miyamoto R, Ueno H, Matsumoto M, Kaji R, Kitaguchi H, Yukitake M, Higashi Y, Nishinaka K, Oda M, Izumi Y, Kawakami H. Sugihara K, et al. Among authors: morino h. Mov Disord. 2012 Aug;27(9):1158-63. doi: 10.1002/mds.25092. Epub 2012 Jul 2. Mov Disord. 2012. PMID: 22753339

8

Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease.

Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H. Izumi Y, et al. Among authors: morino h. Neurology. 2013 Feb 5;80(6):600-1. doi: 10.1212/WNL.0b013e3182815529. Epub 2013 Jan 16. Neurology. 2013. PMID: 23325900 No abstract available.

9

Convenient diagnosis of spinal and bulbar muscular atrophy using a microchip electrophoresis system.

Maruyama H, Morino H, Izumi Y, Noda K, Kawakami H. Maruyama H, et al. Among authors: morino h. Am J Neurodegener Dis. 2013;2(1):35-9. Epub 2013 Mar 8. Am J Neurodegener Dis. 2013. PMID: 23515294 Free PMC article.

10

Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia.

Maruyama H, Morino H, Miyamoto R, Murakami N, Hamano T, Kawakami H. Maruyama H, et al. Among authors: morino h. Clin Genet. 2014 Mar;85(3):296-7. doi: 10.1111/cge.12140. Epub 2013 Apr 4. Clin Genet. 2014. PMID: 23551081 No abstract available.

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