Ikeda S - Search Results

1

Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.

Nakamura A, Yoshida K, Fukushima K, Ueda H, Urasawa N, Koyama J, Yazaki Y, Yazaki M, Sakai T, Haruta S, Takeda S, Ikeda S. Nakamura A, et al. Among authors: ikeda s. J Clin Neurosci. 2008 Jul;15(7):757-63. doi: 10.1016/j.jocn.2006.12.012. Epub 2008 Feb 7. J Clin Neurosci. 2008. PMID: 18261911

2

[Barth syndrome (X linked cardioskeletal myopathy and neutropenia)].

Nakamura A, Ikeda S. Nakamura A, et al. Among authors: ikeda s. Nihon Rinsho. 2002 Apr;60 Suppl 4:389-91. Nihon Rinsho. 2002. PMID: 12013894 Review. Japanese. No abstract available.

3

Progression of dystrophic features and activation of mitogen-activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice.

Nakamura A, Yoshida K, Takeda S, Dohi N, Ikeda S. Nakamura A, et al. Among authors: ikeda s. FEBS Lett. 2002 Jun 5;520(1-3):18-24. doi: 10.1016/s0014-5793(02)02739-4. FEBS Lett. 2002. PMID: 12044863 Free article.

4

Glial fibrillary acidic protein is greatly modified by oxidative stress in aceruloplasminemia brain.

Kaneko K, Nakamura A, Yoshida K, Kametani F, Higuchi K, Ikeda S. Kaneko K, et al. Among authors: ikeda s. Free Radic Res. 2002 Mar;36(3):303-6. doi: 10.1080/10715760290019327. Free Radic Res. 2002. PMID: 12071349

5

Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice.

Yamamoto K, Yoshida K, Miyagoe Y, Ishikawa A, Hanaoka K, Nomoto S, Kaneko K, Ikeda S, Takeda S. Yamamoto K, et al. Among authors: ikeda s. Biochim Biophys Acta. 2002 Dec 12;1588(3):195-202. doi: 10.1016/s0925-4439(02)00165-5. Biochim Biophys Acta. 2002. PMID: 12393173 Free article.

6

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y. Yoshida K, et al. Among authors: ikeda s. Rinsho Shinkeigaku. 2002 Feb;42(2):113-7. Rinsho Shinkeigaku. 2002. PMID: 12424959 Japanese.

7

Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.

Takei Y, Hattori T, Yazaki M, Tokuda T, Urasawa N, Kanai S, Ikeda S. Takei Y, et al. Among authors: ikeda s. Amyloid. 2003 Mar;10(1):25-8. doi: 10.3109/13506120308995253. Amyloid. 2003. PMID: 12762138

8

Usefulness of [123I]metaiodobenzylguanidine ([123I]MIBG) myocardial scintigraphy in differentiating between Alzheimer's disease and dementia with Lewy bodies.

Oide T, Tokuda T, Momose M, Oguchi K, Nakamura A, Ohara S, Ikeda S. Oide T, et al. Among authors: ikeda s. Intern Med. 2003 Aug;42(8):686-90. doi: 10.2169/internalmedicine.42.686. Intern Med. 2003. PMID: 12924492 Free article.

9

Abdominal fat aspiration biopsy and genotyping of serum amyloid A contribute to early diagnosis of reactive AA amyloidosis secondary to rheumatoid arthritis.

Ishii W, Matsuda M, Nakamura A, Nakamura N, Suzuki A, Ikeda S. Ishii W, et al. Among authors: ikeda s. Intern Med. 2003 Sep;42(9):800-5. doi: 10.2169/internalmedicine.42.800. Intern Med. 2003. PMID: 14518665 Free article.

10

Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6.

Hashimoto T, Sasaki O, Yoshida K, Takei Y, Ikeda S. Hashimoto T, et al. Among authors: ikeda s. Mov Disord. 2003 Oct;18(10):1201-4. doi: 10.1002/mds.10511. Mov Disord. 2003. PMID: 14534930

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