Kusunoki S - 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: kusunoki s. Sci Rep. 2023 Oct 18;13(1):17801. doi: 10.1038/s41598-023-45011-8. Sci Rep. 2023. PMID: 37853169 Free PMC article.

2

Amyotrophic lateral sclerosis with IgM antibody against gangliosides GM2 and GD2.

Mizutani K, Oka N, Kusunoki S, Kaji R, Kanda M, Akiguchi I, Shibasaki H. Mizutani K, et al. Among authors: kusunoki s. Intern Med. 2003 Mar;42(3):277-80. doi: 10.2169/internalmedicine.42.277. Intern Med. 2003. PMID: 12705795 Free article.

3

[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: kusunoki s. Rinsho Shinkeigaku. 2008 Mar;48(3):179-83. doi: 10.5692/clinicalneurol.48.179. Rinsho Shinkeigaku. 2008. PMID: 18409537 Japanese.

4

Complete recovery of an aged patient with Guillain-Barré syndrome associated with multiple IgM anti-ganglioside antibodies.

Furiya Y, Hirano M, Kusunoki S, Ueda M, Sugie K, Nishiwaki T, Ueno S. Furiya Y, et al. Among authors: kusunoki s. Muscle Nerve. 2008 Dec;38(6):1630-3. doi: 10.1002/mus.21131. Muscle Nerve. 2008. PMID: 19016534

5

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. Among authors: kusunoki s. 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

6

Abnormal cystatin C levels in two patients with bardet-biedl syndrome.

Hirano M, Ohishi M, Yamashita T, Ikuno Y, Iwahashi H, Mano T, Ishihara R, Tanaka I, Yanagihara K, Isono C, Sakamoto H, Nakamura Y, Kusunoki S. Hirano M, et al. Among authors: kusunoki s. Clin Med Insights Case Rep. 2011;4:17-20. doi: 10.4137/CCRep.S6622. Epub 2011 Mar 10. Clin Med Insights Case Rep. 2011. PMID: 21769262 Free PMC article.

7

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: kusunoki s. 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

8

Antibodies to LM1 and LM1-containing ganglioside complexes in Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy.

Kuwahara M, Suzuki S, Takada K, Kusunoki S. Kuwahara M, et al. Among authors: kusunoki s. J Neuroimmunol. 2011 Oct 28;239(1-2):87-90. doi: 10.1016/j.jneuroim.2011.08.016. Epub 2011 Sep 13. J Neuroimmunol. 2011. PMID: 21914557

9

Risks of inappropriate secretion of antidiuretic hormone in multiple system atrophy.

Samukawa M, Hirano M, Sakamoto H, Kitada M, Kusunoki S, Nakamura Y. Samukawa M, et al. Among authors: kusunoki s. Mov Disord. 2011 Dec;26(14):2572-3. doi: 10.1002/mds.23904. Epub 2011 Oct 10. Mov Disord. 2011. PMID: 21987432 No abstract available.

10

Intravenous immunoglobulin (IVIg) with methylprednisolone pulse therapy for motor impairment of neuralgic amyotrophy: clinical observations in 10 cases.

Naito KS, Fukushima K, Suzuki S, Kuwahara M, Morita H, Kusunoki S, Ikeda S. Naito KS, et al. Among authors: kusunoki s. Intern Med. 2012;51(12):1493-500. doi: 10.2169/internalmedicine.51.7049. Epub 2012 Jun 15. Intern Med. 2012. PMID: 22728480 Free article.

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