Kusunoki S - Search Results

1

Bardet-Biedl syndrome and related disorders in Japan.

Hirano M, Satake W, Moriyama N, Saida K, Okamoto N, Cha PC, Suzuki Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: kusunoki s. J Hum Genet. 2020 Oct;65(10):847-853. doi: 10.1038/s10038-020-0778-y. Epub 2020 May 25. J Hum Genet. 2020. PMID: 32451492

2

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

3

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.

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: 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

5

Refractory acute disseminated encephalomyelitis with anti-galactocerebroside antibody.

Samukawa M, Hirano M, Tsugawa J, Sakamoto H, Tabata E, Takada K, Kuwahara M, Suzuki S, Kitada M, Yamada T, Hara H, Tsuboi Y, Nakamura Y, Kusunoki S. Samukawa M, et al. Among authors: kusunoki s. Neurosci Res. 2012 Dec;74(3-4):284-9. doi: 10.1016/j.neures.2012.09.006. Epub 2012 Oct 17. Neurosci Res. 2012. PMID: 23085407

6

Details of treatment-related difficulties in men with anti-N-methyl-D-aspartate receptor encephalitis.

Sakamoto H, Hirano M, Samukawa M, Ueno S, Maekura S, Fujimura H, Kuwahara M, Hamada Y, Isono C, Tanaka K, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: kusunoki s. Eur Neurol. 2013;69(1):21-6. doi: 10.1159/000342023. Epub 2012 Nov 1. Eur Neurol. 2013. PMID: 23128856

7

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: kusunoki s. Neurology. 2013 Jan 29;80(5):458-63. doi: 10.1212/WNL.0b013e31827f0fe5. Epub 2013 Jan 9. Neurology. 2013. PMID: 23303844

8

Differences in dysphagia between spinocerebellar ataxia type 3 and type 6.

Isono C, Hirano M, Sakamoto H, Ueno S, Kusunoki S, Nakamura Y. Isono C, et al. Among authors: kusunoki s. Dysphagia. 2013 Sep;28(3):413-8. doi: 10.1007/s00455-013-9450-4. Epub 2013 Mar 21. Dysphagia. 2013. PMID: 23515636

9

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

Multiple-System Atrophy Research Collaboration. Multiple-System Atrophy Research Collaboration. N Engl J Med. 2013 Jul 18;369(3):233-44. doi: 10.1056/NEJMoa1212115. Epub 2013 Jun 12. N Engl J Med. 2013. PMID: 23758206 Free article.

10

Clinical features in Guillain-Barré syndrome with anti-Gal-C antibody.

Samukawa M, Hamada Y, Kuwahara M, Takada K, Hirano M, Mitsui Y, Sonoo M, Kusunoki S; Japanese GBS Study Group. Samukawa M, et al. Among authors: kusunoki s. J Neurol Sci. 2014 Feb 15;337(1-2):55-60. doi: 10.1016/j.jns.2013.11.016. Epub 2013 Nov 19. J Neurol Sci. 2014. PMID: 24289889

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