Saigoh K - Search Results

1

CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.

Hirano M, Kuwahara M, Yamagishi Y, Samukawa M, Fujii K, Yamashita S, Ando M, Oka N, Nagano M, Matsui T, Takeuchi T, Saigoh K, Kusunoki S, Takashima H, Nagai Y. Hirano M, et al. Among authors: saigoh k. Sci Rep. 2023 Oct 18;13(1):17801. doi: 10.1038/s41598-023-45011-8. Sci Rep. 2023. PMID: 37853169 Free PMC article.

2

Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene.

Hirano M, Samukawa M, Isono C, Saigoh K, Nakamura Y, Kusunoki S. Hirano M, et al. Among authors: saigoh k. Neurol Genet. 2018 Aug 1;4(4):e252. doi: 10.1212/NXG.0000000000000252. eCollection 2018 Aug. Neurol Genet. 2018. PMID: 30109267 Free PMC article.

3

Effect of expression alteration in flanking genes on phenotypes of St8sia2-deficient mice.

Ikegami K, Saigoh K, Fujioka A, Nagano M, Kitajima K, Sato C, Masubuchi S, Kusunoki S, Shigeyoshi Y. Ikegami K, et al. Among authors: saigoh k. Sci Rep. 2019 Sep 20;9(1):13634. doi: 10.1038/s41598-019-50006-5. Sci Rep. 2019. PMID: 31541165 Free PMC article.

4

Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan.

Inada R, Hirano M, Oka N, Samukawa M, Saigoh K, Suzuki H, Udaka F, Hashiguchi A, Takashima H, Hamada Y, Nakamura Y, Kusunoki S. Inada R, et al. Among authors: saigoh k. J Neurol. 2021 Aug;268(8):2933-2942. doi: 10.1007/s00415-021-10467-z. Epub 2021 Feb 24. J Neurol. 2021. PMID: 33625581

5

Memantine administration prevented chorea movement in Huntington's disease: a case report.

Saigoh K, Hirano M, Mitsui Y, Oda I, Ikegawa A, Samukawa M, Yoshikawa K, Yamagishi Y, Kusunoki S, Nagai Y. Saigoh K, et al. J Med Case Rep. 2023 Oct 16;17(1):431. doi: 10.1186/s13256-023-04161-z. J Med Case Rep. 2023. PMID: 37840138 Free PMC article.

6

PSP-Phenotype in SCA8: Case Report and Systemic Review.

Samukawa M, Hirano M, Saigoh K, Kawai S, Hamada Y, Takahashi D, Nakamura Y, Kusunoki S. Samukawa M, et al. Among authors: saigoh k. Cerebellum. 2019 Feb;18(1):76-84. doi: 10.1007/s12311-018-0955-0. Cerebellum. 2019. PMID: 29916049

7

The novel de novo mutation of KIF1A gene as the cause for Spastic paraplegia 30 in a Japanese case.

Yoshikawa K, Kuwahara M, Saigoh K, Ishiura H, Yamagishi Y, Hamano Y, Samukawa M, Suzuki H, Hirano M, Mitsui Y, Tsuji S, Kusunoki S. Yoshikawa K, et al. Among authors: saigoh k. eNeurologicalSci. 2018 Nov 22;14:34-37. doi: 10.1016/j.ensci.2018.11.026. eCollection 2019 Mar. eNeurologicalSci. 2018. PMID: 30582020 Free PMC article.

8

Charcot-Marie-Tooth disease with a mutation in FBLN5 accompanying with the small vasculitis and widespread onion-bulb formations.

Yamagishi Y, Samukawa M, Kuwahara M, Takada K, Saigoh K, Mitsui Y, Oka N, Hashiguchi A, Takashima H, Kusunoki S. Yamagishi Y, et al. Among authors: saigoh k. J Neurol Sci. 2020 Mar 15;410:116623. doi: 10.1016/j.jns.2019.116623. Epub 2019 Dec 9. J Neurol Sci. 2020. PMID: 31945625 No abstract available.

9

Time Course of Radiological Imaging and Variable Interindividual Symptoms in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated with p.Arg487His Mutation in the VCP Gene.

Hirano M, Yamagishi Y, Yanagimoto S, Saigoh K, Nakamura Y, Kusunoki S. Hirano M, et al. Among authors: saigoh k. Eur Neurol. 2017;78(1-2):78-83. doi: 10.1159/000478906. Epub 2017 Jul 24. Eur Neurol. 2017. PMID: 28738334

10

Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.

Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: saigoh k. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Jun;15(3-4):312-4. doi: 10.3109/21678421.2013.873051. Epub 2014 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24611504

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