Murayama S - Search Results

1

β-N-methylamino-l-alanine analysis in the brains of patients with Kii ALS/PDC.

Kokubo Y, Banack SA, Morimoto S, Murayama S, Togashi T, Metcalf JS, Cox PA, Kuzuhara S. Kokubo Y, et al. Among authors: murayama s. Neurology. 2017 Sep 5;89(10):1091-1092. doi: 10.1212/WNL.0000000000004310. Epub 2017 Aug 9. Neurology. 2017. PMID: 28794246 No abstract available.

2

Prospective 10-year surveillance of human prion diseases in Japan.

Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, Takeda M, Kuroda S, Abe K, Murai H, Murayama S, Tateishi J, Takumi I, Shirabe S, Harada M, Sadakane A, Yamada M. Nozaki I, et al. Among authors: murayama s. Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20. Brain. 2010. PMID: 20855418

3

Cardiac ¹²³I-meta-iodobenzylguanidine scintigraphy and lewy body pathology in a patient with amyotrophic lateral sclerosis and parkinsonism-dementia complex of Kii, Japan.

Kokubo Y, Morimoto S, Shindo A, Hirokawa Y, Shiraishi T, Saito Y, Murayama S, Kuzuhara S. Kokubo Y, et al. Among authors: murayama s. Mov Disord. 2011 Oct;26(12):2300-1. doi: 10.1002/mds.23850. Epub 2011 Jul 20. Mov Disord. 2011. PMID: 21780178 No abstract available.

4

[Clinical and pathological characteristics of FUS/TLS-associated amyotrophic lateral sclerosis (ALS)].

Murayama S. Murayama S. Rinsho Shinkeigaku. 2010 Nov;50(11):948-50. doi: 10.5692/clinicalneurol.50.948. Rinsho Shinkeigaku. 2010. PMID: 21921522 Japanese.

5

Mutational analysis of familial and sporadic amyotrophic lateral sclerosis with OPTN mutations in Japanese population.

Naruse H, Takahashi Y, Kihira T, Yoshida S, Kokubo Y, Kuzuhara S, Ishiura H, Amagasa M, Murayama S, Tsuji S, Goto J. Naruse H, et al. Among authors: murayama s. Amyotroph Lateral Scler. 2012 Oct;13(6):562-6. doi: 10.3109/17482968.2012.684213. Epub 2012 Jun 18. Amyotroph Lateral Scler. 2012. PMID: 22708870

6

α-Synuclein pathology in the amyotrophic lateral sclerosis/parkinsonism dementia complex in the Kii Peninsula, Japan.

Kokubo Y, Taniguchi A, Hasegawa M, Hayakawa Y, Morimoto S, Yoneda M, Hirokawa Y, Shiraishi T, Saito Y, Murayama S, Kuzuhara S. Kokubo Y, et al. Among authors: murayama s. J Neuropathol Exp Neurol. 2012 Jul;71(7):625-30. doi: 10.1097/NEN.0b013e31825b9680. J Neuropathol Exp Neurol. 2012. PMID: 22710962

7

Molecular analysis and biochemical classification of TDP-43 proteinopathy.

Tsuji H, Arai T, Kametani F, Nonaka T, Yamashita M, Suzukake M, Hosokawa M, Yoshida M, Hatsuta H, Takao M, Saito Y, Murayama S, Akiyama H, Hasegawa M, Mann DM, Tamaoka A. Tsuji H, et al. Among authors: murayama s. Brain. 2012 Nov;135(Pt 11):3380-91. doi: 10.1093/brain/aws230. Epub 2012 Oct 3. Brain. 2012. PMID: 23035040

8

[Prognosis of amyotrophic lateral sclerosis in relation with pathological pattern of propagation].

Murayama S, Saito Y. Murayama S, et al. Rinsho Shinkeigaku. 2012;52(11):1066-7. doi: 10.5692/clinicalneurol.52.1066. Rinsho Shinkeigaku. 2012. PMID: 23196517 Japanese. No abstract available.

9

[A Case of Corticobasal Syndrome Complicated with Hypopituitarism and Hashimoto's Disease].

Morimoto S, Kinbara Y, Terada M, Komiya T, Ishii K, Takao M, Kanemaru K, Murayama S. Morimoto S, et al. Among authors: murayama s. Brain Nerve. 2015 Jun;67(6):759-64. doi: 10.11477/mf.1416200213. Brain Nerve. 2015. PMID: 26062591 Japanese.

10

The feasibility of white matter volume reduction analysis using SPM8 plus DARTEL for the diagnosis of patients with clinically diagnosed corticobasal syndrome and Richardson's syndrome.

Sakurai K, Imabayashi E, Tokumaru AM, Hasebe S, Murayama S, Morimoto S, Kanemaru K, Takao M, Shibamoto Y, Matsukawa N. Sakurai K, et al. Among authors: murayama s. Neuroimage Clin. 2014 Feb 27;7:605-10. doi: 10.1016/j.nicl.2014.02.009. eCollection 2015. Neuroimage Clin. 2014. PMID: 26082887 Free PMC article.

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