Oya Y - Search Results

1

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.

Deng J, Yu J, Li P, Luan X, Cao L, Zhao J, Yu M, Zhang W, Lv H, Xie Z, Meng L, Zheng Y, Zhao Y, Gang Q, Wang Q, Liu J, Zhu M, Guo X, Su Y, Liang Y, Liang F, Hayashi T, Maeda MH, Sato T, Ura S, Oya Y, Ogasawara M, Iida A, Nishino I, Zhou C, Yan C, Yuan Y, Hong D, Wang Z. Deng J, et al. Among authors: oya y. Am J Hum Genet. 2020 Jun 4;106(6):793-804. doi: 10.1016/j.ajhg.2020.04.011. Epub 2020 May 14. Am J Hum Genet. 2020. PMID: 32413282 Free PMC article.

2

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.

Noguchi S, Keira Y, Murayama K, Ogawa M, Fujita M, Kawahara G, Oya Y, Imazawa M, Goto Y, Hayashi YK, Nonaka I, Nishino I. Noguchi S, et al. Among authors: oya y. J Biol Chem. 2004 Mar 19;279(12):11402-7. doi: 10.1074/jbc.M313171200. Epub 2004 Jan 5. J Biol Chem. 2004. PMID: 14707127 Free article.

3

FSHD-like patients without 4q35 deletion.

Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK. Yamanaka G, et al. Among authors: oya y. J Neurol Sci. 2004 Apr 15;219(1-2):89-93. doi: 10.1016/j.jns.2003.12.010. J Neurol Sci. 2004. PMID: 15050443

4

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy.

Arimura T, Hayashi YK, Murakami T, Oya Y, Funabe S, Arikawa-Hirasawa E, Hattori N, Nishino I, Kimura A. Arimura T, et al. Among authors: oya y. Circ J. 2009 Jan;73(1):158-61. doi: 10.1253/circj.cj-08-0722. Epub 2008 Nov 17. Circ J. 2009. PMID: 19015585 Free article.

5

[Limb-girdle muscular dystrophy type 2M with adult-onset loss of ambulation. A case report].

Kondo Y, Mori-Yoshimura M, Hayashi YK, Oya Y, Satoh N, Nishino I, Murata M. Kondo Y, et al. Among authors: oya y. Rinsho Shinkeigaku. 2010 Sep;50(9):661-5. doi: 10.5692/clinicalneurol.50.661. Rinsho Shinkeigaku. 2010. PMID: 20960933 Japanese.

6

Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathology.

Tsuburaya RS, Monma K, Oya Y, Nakayama T, Fukuda T, Sugie H, Hayashi YK, Nonaka I, Nishino I. Tsuburaya RS, et al. Among authors: oya y. Neuromuscul Disord. 2012 May;22(5):389-93. doi: 10.1016/j.nmd.2011.11.003. Epub 2011 Dec 21. Neuromuscul Disord. 2012. PMID: 22196155

7

Clinicopathological features of centronuclear myopathy in Japanese populations harboring mutations in dynamin 2.

Mori-Yoshimura M, Okuma A, Oya Y, Fujimura-Kiyono C, Nakajima H, Matsuura K, Takemura A, Malicdan MC, Hayashi YK, Nonaka I, Murata M, Nishino I. Mori-Yoshimura M, et al. Among authors: oya y. Clin Neurol Neurosurg. 2012 Jul;114(6):678-83. doi: 10.1016/j.clineuro.2011.10.040. Epub 2012 May 19. Clin Neurol Neurosurg. 2012. PMID: 22613877

8

Respiratory dysfunction in patients severely affected by GNE myopathy (distal myopathy with rimmed vacuoles).

Mori-Yoshimura M, Oya Y, Hayashi YK, Noguchi S, Nishino I, Murata M. Mori-Yoshimura M, et al. Among authors: oya y. Neuromuscul Disord. 2013 Jan;23(1):84-8. doi: 10.1016/j.nmd.2012.09.007. Epub 2012 Nov 2. Neuromuscul Disord. 2013. PMID: 23127962

9

DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.

Sato T, Hayashi YK, Oya Y, Kondo T, Sugie K, Kaneda D, Houzen H, Yabe I, Sasaki H, Noguchi S, Nonaka I, Osawa M, Nishino I. Sato T, et al. Among authors: oya y. Neuromuscul Disord. 2013 Mar;23(3):269-76. doi: 10.1016/j.nmd.2012.12.010. Epub 2013 Feb 6. Neuromuscul Disord. 2013. PMID: 23394708

10

Mutation profile of the GNE gene in Japanese patients with distal myopathy with rimmed vacuoles (GNE myopathy).

Cho A, Hayashi YK, Monma K, Oya Y, Noguchi S, Nonaka I, Nishino I. Cho A, et al. Among authors: oya y. J Neurol Neurosurg Psychiatry. 2014 Aug;85(8):914-7. doi: 10.1136/jnnp-2013-305587. Epub 2013 Sep 11. J Neurol Neurosurg Psychiatry. 2014. PMID: 24027297

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