Saigoh K - Search Results

1

Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review.

Samukawa M, Nakamura N, Hirano M, Morikawa M, Sakata H, Nishino I, Izumi R, Suzuki N, Kuroda H, Shiga K, Saigoh K, Aoki M, Kusunoki S. Samukawa M, et al. Among authors: saigoh k. Eur Neurol. 2020;83(3):317-322. doi: 10.1159/000508346. Epub 2020 Jun 19. Eur Neurol. 2020. PMID: 32564019 Free PMC article. Review.

2

[Case of Gerstmann-Sträussler-Scheinker syndrome (GSS-P102L) mimicking variant Creurtzfeldt-Jakob disease in clinical manifestation and MRI findings].

Kanata A, Saigoh K, Mitsui Y, Kitamoto T, Kusunoki S. Kanata A, et al. Among authors: saigoh k. Rinsho Shinkeigaku. 2008 Mar;48(3):179-83. doi: 10.5692/clinicalneurol.48.179. Rinsho Shinkeigaku. 2008. PMID: 18409537 Japanese.

3

Chondroitin beta-1,4-N-acetylgalactosaminyltransferase-1 missense mutations are associated with neuropathies.

Saigoh K, Izumikawa T, Koike T, Shimizu J, Kitagawa H, Kusunoki S. Saigoh K, et al. J Hum Genet. 2011 Feb;56(2):143-6. doi: 10.1038/jhg.2010.148. Epub 2010 Dec 16. J Hum Genet. 2011. PMID: 21160489

4

A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.

Hirano M, Kokunai Y, Nagai A, Nakamura Y, Saigoh K, Kusunoki S, Takahashi MP. Hirano M, et al. Among authors: saigoh k. J Neurol Sci. 2011 Oct 15;309(1-2):9-11. doi: 10.1016/j.jns.2011.07.046. Epub 2011 Aug 19. J Neurol Sci. 2011. PMID: 21855088

5

Circadian expression and specific localization of a sialyltransferase gene in the suprachiasmatic nucleus.

Hamada Y, Saigoh K, Masumoto KH, Nagano M, Kusunoki S, Shigeyoshi Y. Hamada Y, et al. Among authors: saigoh k. Neurosci Lett. 2013 Feb 22;535:12-7. doi: 10.1016/j.neulet.2012.12.032. Epub 2013 Jan 5. Neurosci Lett. 2013. PMID: 23298785

6

Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis.

Hirano M, Nakamura Y, Saigoh K, Sakamoto H, Ueno S, Isono C, Miyamoto K, Akamatsu M, Mitsui Y, Kusunoki S. Hirano M, et al. Among authors: saigoh k. Neurology. 2013 Jan 29;80(5):458-63. doi: 10.1212/WNL.0b013e31827f0fe5. Epub 2013 Jan 9. Neurology. 2013. PMID: 23303844

7

A chondroitin synthase-1 (ChSy-1) missense mutation in a patient with neuropathy impairs the elongation of chondroitin sulfate chains initiated by chondroitin N-acetylgalactosaminyltransferase-1.

Izumikawa T, Saigoh K, Shimizu J, Tsuji S, Kusunoki S, Kitagawa H. Izumikawa T, et al. Among authors: saigoh k. Biochim Biophys Acta. 2013 Oct;1830(10):4806-12. doi: 10.1016/j.bbagen.2013.06.017. Epub 2013 Jun 27. Biochim Biophys Acta. 2013. PMID: 23811343

8

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

9

[The significance of oxidized DJ-1 protein (oxDJ-1) as a biomarker for Parkinson's disease].

Ogawa I, Saito Y, Saigoh K, Hosoi Y, Mitsui Y, Noguchi N, Kusunoki S. Ogawa I, et al. Among authors: saigoh k. Brain Nerve. 2014 Apr;66(4):471-7. Brain Nerve. 2014. PMID: 24748095 Japanese.

10

VCP gene analyses in Japanese patients with sporadic amyotrophic lateral sclerosis identify a new mutation.

Hirano M, Nakamura Y, Saigoh K, Sakamoto H, Ueno S, Isono C, Mitsui Y, Kusunoki S. Hirano M, et al. Among authors: saigoh k. Neurobiol Aging. 2015 Mar;36(3):1604.e1-6. doi: 10.1016/j.neurobiolaging.2014.10.012. Epub 2014 Oct 16. Neurobiol Aging. 2015. PMID: 25457024

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