Ikeda S - Search Results

1

Ikeda M, Hirano M, Shinoda K, Katsumata N, Furutama D, Nakamura K, Ikeda S, Tanaka T, Hanafusa T, Kitajima H, Kohno H, Nakagawa M, Nakamura Y, Ueno S. Ikeda M, et al. Among authors: ikeda s. Muscle Nerve. 2013 Sep;48(3):381-6. doi: 10.1002/mus.23770. Epub 2013 Jul 17. Muscle Nerve. 2013. PMID: 23861206

2

Adult or late-onset triple A syndrome: case report and literature review.

Nakamura K, Yoshida K, Yoshinaga T, Kodaira M, Shimojima Y, Takei Y, Morita H, Kayanuma K, Ikeda S. Nakamura K, et al. Among authors: ikeda s. J Neurol Sci. 2010 Oct 15;297(1-2):85-8. doi: 10.1016/j.jns.2010.07.006. Epub 2010 Aug 1. J Neurol Sci. 2010. PMID: 20674935 Review.

3

A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea.

Nakamura K, Sekijima Y, Nagamatsu K, Yoshida K, Ikeda S. Nakamura K, et al. Among authors: ikeda s. J Neurol Sci. 2012 Feb 15;313(1-2):189-92. doi: 10.1016/j.jns.2011.09.013. Epub 2011 Oct 5. J Neurol Sci. 2012. PMID: 21982616 Free article. Review.

4

A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2).

Nakamura K, Yoshida K, Makishita H, Kitamura E, Hashimoto S, Ikeda S. Nakamura K, et al. Among authors: ikeda s. J Hum Genet. 2009 Dec;54(12):746-8. doi: 10.1038/jhg.2009.104. Epub 2009 Nov 6. J Hum Genet. 2009. PMID: 19893583

5

Spinocerebellar ataxia type 6 (SCA6): clinical pilot trial with gabapentin.

Nakamura K, Yoshida K, Miyazaki D, Morita H, Ikeda S. Nakamura K, et al. Among authors: ikeda s. J Neurol Sci. 2009 Mar 15;278(1-2):107-11. doi: 10.1016/j.jns.2008.12.017. Epub 2009 Jan 21. J Neurol Sci. 2009. PMID: 19157422 Free article. Clinical Trial.

6

Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene.

Sekijima Y, Nakamura K, Kishida D, Narita A, Adachi K, Ohno K, Nanba E, Ikeda S. Sekijima Y, et al. Among authors: ikeda s. Intern Med. 2013;52(1):119-24. doi: 10.2169/internalmedicine.52.8901. Epub 2013 Jan 1. Intern Med. 2013. PMID: 23291686 Free article.

7

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation.

Shimazaki H, Honda J, Naoi T, Namekawa M, Nakano I, Yazaki M, Nakamura K, Yoshida K, Ikeda S, Ishiura H, Fukuda Y, Takahashi Y, Goto J, Tsuji S, Takiyama Y. Shimazaki H, et al. Among authors: ikeda s. J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):1024-8. doi: 10.1136/jnnp-2013-306981. Epub 2014 Feb 12. J Neurol Neurosurg Psychiatry. 2014. PMID: 24521565

8

Hypertrophic Pachymeningitis as an Early Manifestation of Relapsing Polychondritis: Case Report and Review of the Literature.

Ushiyama S, Kinoshita T, Shimojima Y, Ohashi N, Kishida D, Miyazaki D, Nakamura K, Sekijima Y, Ikeda SI. Ushiyama S, et al. Among authors: ikeda si. Case Rep Neurol. 2016 Oct 31;8(3):211-217. doi: 10.1159/000450850. eCollection 2016 Sep-Dec. Case Rep Neurol. 2016. PMID: 27920712 Free PMC article.

9

Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients.

Nagamatsu K, Sekijima Y, Nakamura K, Nakamura K, Hattori K, Ota M, Shimizu Y, Endo F, Ikeda SI. Nagamatsu K, et al. J Hum Genet. 2017 Jul;62(7):665-670. doi: 10.1038/jhg.2017.31. Epub 2017 Mar 9. J Hum Genet. 2017. PMID: 28275245

10

Severity and progression rate of cerebellar ataxia in 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA) in the endemic Nagano Area of Japan.

Yoshida K, Shimizu Y, Morita H, Okano T, Sakai H, Ohata T, Matsumoto N, Nakamura K, Tazawa K, Ohara S, Tabata K, Inoue A, Sato S, Shimojima Y, Hattori T, Ushiyama M, Ikeda S. Yoshida K, et al. Among authors: ikeda s. Cerebellum. 2009 Mar;8(1):46-51. doi: 10.1007/s12311-008-0062-8. Cerebellum. 2009. PMID: 18855094

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