Yazaki M - Search Results

1

Identification of Disease-Promoting HLA Class I and Protective Class II Modifiers in Japanese Patients with Familial Mediterranean Fever.

Yasunami M, Nakamura H, Agematsu K, Nakamura A, Yazaki M, Kishida D, Yachie A, Toma T, Masumoto J, Ida H, Koga T, Kawakami A, Eguchi K, Furukawa H, Nakamura T, Nakamura M, Migita K. Yasunami M, et al. Among authors: yazaki m. PLoS One. 2015 May 14;10(5):e0125938. doi: 10.1371/journal.pone.0125938. eCollection 2015. PLoS One. 2015. PMID: 25974247 Free PMC article.

2

[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.

3

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

4

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

5

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

6

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.

7

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.

8

Severe protein losing enteropathy with intractable diarrhea due to systemic AA amyloidosis, successfully treated with corticosteroid and octreotide.

Fushimi T, Takahashi Y, Kashima Y, Fukushima K, Ishii W, Kaneko K, Yazaki M, Nakamura A, Tokuda T, Matsuda M, Furuya R, Ikeda S. Fushimi T, et al. Among authors: yazaki m. Amyloid. 2005 Mar;12(1):48-53. doi: 10.1080/13506120500032725. Amyloid. 2005. PMID: 16076611

9

A Japanese case of familial Mediterranean fever with homozygosity for the pyrin E148Q mutation.

Suzuki T, Nakamura A, Yazaki M, Ikeda S. Suzuki T, et al. Among authors: yazaki m. Intern Med. 2005 Jul;44(7):765-6. doi: 10.2169/internalmedicine.44.765. Intern Med. 2005. PMID: 16093605 Free article. No abstract available.

10

Adult onset X-linked chronic granulomatous disease in a woman patient caused by a de novo mutation in paternal-origin CYBB gene and skewed inactivation of normal maternal X chromosome.

Gono T, Yazaki M, Agematsu K, Matsuda M, Yasui K, Yamaura M, Hidaka F, Mizukami T, Nunoi H, Kubota T, Ikeda S. Gono T, et al. Among authors: yazaki m. Intern Med. 2008;47(11):1053-6. doi: 10.2169/internalmedicine.47.0919. Epub 2008 Jun 2. Intern Med. 2008. PMID: 18520120 Free article.

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