Yazaki M - Search Results

1

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

2

[Familial amyloid polyneuropathy type IV (Finnish type)--a clinicopathological study].

Makishita H, Yazaki M, Matsuda M, Ikeda S, Yanagisawa N. Makishita H, et al. Among authors: yazaki m. Rinsho Shinkeigaku. 1994 May;34(5):431-7. Rinsho Shinkeigaku. 1994. PMID: 7924053 Clinical Trial. Japanese.

3

[A case of transverse myelopathy caused by pyogenic vertebral osteomyelitis having extended from a pedal ulcer].

Yazaki M, Tokuda T, Matsuda M, Shindo M, Yanagisawa N. Yazaki M, et al. Rinsho Shinkeigaku. 1994 Apr;34(4):371-6. Rinsho Shinkeigaku. 1994. PMID: 8026133 Japanese.

4

Complete neurological recovery of an adult patient with type II citrullinemia after living related partial liver transplantation.

Yazaki M, Ikeda S, Takei Y, Yanagisawa N, Matsunami H, Hashikura Y, Kawasaki S, Makuuchi M, Kobayashi K, Saheki T. Yazaki M, et al. Transplantation. 1996 Dec 15;62(11):1679-84. doi: 10.1097/00007890-199612150-00027. Transplantation. 1996. PMID: 8970629

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

[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.

7

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

8

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

9

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

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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