Riku Y - Search Results

1

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.

Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M. Yoshida T, et al. Among authors: riku y. Acta Neurol Scand. 2011 Aug;124(2):104-8. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849398

2

CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.

Kume K, Kurashige T, Muguruma K, Morino H, Tada Y, Kikumoto M, Miyamoto T, Akutsu SN, Matsuda Y, Matsuura S, Nakamori M, Nishiyama A, Izumi R, Niihori T, Ogasawara M, Eura N, Kato T, Yokomura M, Nakayama Y, Ito H, Nakamura M, Saito K, Riku Y, Iwasaki Y, Maruyama H, Aoki Y, Nishino I, Izumi Y, Aoki M, Kawakami H. Kume K, et al. Among authors: riku y. Am J Hum Genet. 2023 Jul 6;110(7):1086-1097. doi: 10.1016/j.ajhg.2023.05.014. Epub 2023 Jun 19. Am J Hum Genet. 2023. PMID: 37339631 Free PMC article.

3

VZV vasculopathy associated with myelo-radiculoganglio-meningo-encephalitis: an autopsy case of an immunocompetent 66-year-old male.

Miyazaki Y, Riku Y, Goto Y, Mano K, Yoshida M, Hashizume Y. Miyazaki Y, et al. Among authors: riku y. J Neurol Sci. 2008 Dec 15;275(1-2):42-5. doi: 10.1016/j.jns.2008.07.019. Epub 2008 Aug 30. J Neurol Sci. 2008. PMID: 18757065

4

[Is hypertrophic pachymeningitis a dural lesion of IgG4-related systemic disease?].

Riku S, Hashizume Y, Yoshida M, Riku Y. Riku S, et al. Among authors: riku y. Rinsho Shinkeigaku. 2009 Sep;49(9):594-6. doi: 10.5692/clinicalneurol.49.594. Rinsho Shinkeigaku. 2009. PMID: 19928692 Japanese.

5

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease.

Yoshida T, Mizuta I, Saito K, Ohara R, Kurisaki H, Ohnari K, Riku Y, Hayashi Y, Suzuki H, Shii H, Fujiwara Y, Yonezu T, Nagaishi A, Nakagawa M. Yoshida T, et al. Among authors: riku y. J Hum Genet. 2013 Sep;58(9):635-8. doi: 10.1038/jhg.2013.83. Epub 2013 Aug 1. J Hum Genet. 2013. PMID: 23903069

6

Extensive aggregation of α-synuclein and tau in juvenile-onset neuroaxonal dystrophy: an autopsied individual with a novel mutation in the PLA2G6 gene-splicing site.

Riku Y, Ikeuchi T, Yoshino H, Mimuro M, Mano K, Goto Y, Hattori N, Sobue G, Yoshida M. Riku Y, et al. Acta Neuropathol Commun. 2013 May 9;1:12. doi: 10.1186/2051-5960-1-12. Acta Neuropathol Commun. 2013. PMID: 24252552 Free PMC article.

7

Lower motor neuron involvement in TAR DNA-binding protein of 43 kDa-related frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Riku Y, Watanabe H, Yoshida M, Tatsumi S, Mimuro M, Iwasaki Y, Katsuno M, Iguchi Y, Masuda M, Senda J, Ishigaki S, Udagawa T, Sobue G. Riku Y, et al. JAMA Neurol. 2014 Feb;71(2):172-9. doi: 10.1001/jamaneurol.2013.5489. JAMA Neurol. 2014. PMID: 24378564

8

Differential motor neuron involvement in progressive muscular atrophy: a comparative study with amyotrophic lateral sclerosis.

Riku Y, Atsuta N, Yoshida M, Tatsumi S, Iwasaki Y, Mimuro M, Watanabe H, Ito M, Senda J, Nakamura R, Koike H, Sobue G. Riku Y, et al. BMJ Open. 2014 May 14;4(5):e005213. doi: 10.1136/bmjopen-2014-005213. BMJ Open. 2014. PMID: 24833696 Free PMC article.

9

Early pathologic changes in hereditary diffuse leukoencephalopathy with spheroids.

Riku Y, Ando T, Goto Y, Mano K, Iwasaki Y, Sobue G, Yoshida M. Riku Y, et al. J Neuropathol Exp Neurol. 2014 Dec;73(12):1183-90. doi: 10.1097/NEN.0000000000000139. J Neuropathol Exp Neurol. 2014. PMID: 25383640

10

Non-motor multiple system atrophy associated with sudden death: pathological observations of autonomic nuclei.

Riku Y, Watanabe H, Mimuro M, Iwasaki Y, Ito M, Katsuno M, Sobue G, Yoshida M. Riku Y, et al. J Neurol. 2017 Nov;264(11):2249-2257. doi: 10.1007/s00415-017-8604-y. Epub 2017 Sep 22. J Neurol. 2017. PMID: 28939940

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