Yazaki M - Search Results

1

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I. Kondo I, et al. Among authors: yazaki m. J Med Genet. 1990 Feb;27(2):105-8. doi: 10.1136/jmg.27.2.105. J Med Genet. 1990. PMID: 1969487 Free PMC article.

2

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.

Yoshida K, Nakamura A, Yazaki M, Ikeda S, Takeda S. Yoshida K, et al. Among authors: yazaki m. Hum Mol Genet. 1998 Jul;7(7):1129-32. doi: 10.1093/hmg/7.7.1129. Hum Mol Genet. 1998. PMID: 9618170

3

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: yazaki y, yazaki m. 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

4

[Correlation of cardiac muscle involvement and the dystrophin gene abnormality in Becker muscular dystrophy].

Yazaki M, Nakamura A, Yoshida K, Ikeda S. Yazaki M, et al. Nihon Rinsho. 1997 Dec;55(12):3142-7. Nihon Rinsho. 1997. PMID: 9436425 Review. Japanese.

5

Up-regulation of the brain and Purkinje-cell forms of dystrophin transcripts, in Becker muscular dystrophy.

Nakamura A, Ikeda S, Yazaki M, Yoshida K, Kobayashi O, Yanagisawa N, Takeda S. Nakamura A, et al. Among authors: yazaki m. Am J Hum Genet. 1997 Jun;60(6):1555-8. Am J Hum Genet. 1997. PMID: 9199582 Free PMC article. No abstract available.

6

A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.

Yazaki M, Yoshida K, Nakamura A, Furihata K, Yonekawa M, Okabe T, Yamashita N, Ohta M, Ikeda S. Yazaki M, et al. J Neurol Sci. 1998;156(1):30-4. doi: 10.1016/s0022-510x(98)00015-x. J Neurol Sci. 1998. PMID: 9559983

7

Clinical characteristics of aged Becker muscular dystrophy patients with onset after 30 years.

Yazaki M, Yoshida K, Nakamura A, Koyama J, Nanba T, Ohori N, Ikeda S. Yazaki M, et al. Eur Neurol. 1999;42(3):145-9. doi: 10.1159/000008089. Eur Neurol. 1999. PMID: 10529540

8

A Japanese patient with familial Mediterranean fever associated with compound heterozygosity for pyrin variant E148Q/M694I.

Nakamura A, Yazaki M, Tokuda T, Hattori T, Ikeda S. Nakamura A, et al. Among authors: yazaki m. Intern Med. 2005 Mar;44(3):261-5. doi: 10.2169/internalmedicine.44.261. Intern Med. 2005. PMID: 15805719 Free article.

9

Cardiac amyloid in patients with familial amyloid polyneuropathy consists of abundant wild-type transthyretin.

Yazaki M, Tokuda T, Nakamura A, Higashikata T, Koyama J, Higuchi K, Harihara Y, Baba S, Kametani F, Ikeda S. Yazaki M, et al. Biochem Biophys Res Commun. 2000 Aug 11;274(3):702-6. doi: 10.1006/bbrc.2000.3203. Biochem Biophys Res Commun. 2000. PMID: 10924339

10

A case of pectoral fasciitis with spontaneous remission.

Fushimi T, Nakamura A, Yazaki M, Shimizu Y, Morita H, Ikeda SI. Fushimi T, et al. Among authors: yazaki m. Eur Neurol. 2000;44(2):124-5. doi: 10.1159/000008212. Eur Neurol. 2000. PMID: 10965169 No abstract available.

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