Yoshida K - Search Results

1

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family.

Hanaoka N, Yoshida K, Nakamura A, Furihata K, Seo T, Tani Y, Takahashi J, Ikeda S, Hanyu N. Hanaoka N, et al. Among authors: yoshida k. J Neurol Sci. 1999 May 1;165(1):6-9. doi: 10.1016/s0022-510x(99)00028-3. J Neurol Sci. 1999. PMID: 10426139

2

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. Among authors: yoshida k. J Neurol Sci. 1998;156(1):30-4. doi: 10.1016/s0022-510x(98)00015-x. J Neurol Sci. 1998. PMID: 9559983

3

[A patient with Kennedy-Alter-Sung syndrome showing cardiomyopathy].

Hattori T, Ikeda S, Yoshida K, Yanagisawa N, Furihata K, Yoshida K. Hattori T, et al. Among authors: yoshida k. Rinsho Shinkeigaku. 1995 Nov;35(11):1246-9. Rinsho Shinkeigaku. 1995. PMID: 8720337 Japanese.

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. Among authors: yoshida k. Nihon Rinsho. 1997 Dec;55(12):3142-7. Nihon Rinsho. 1997. PMID: 9436425 Review. Japanese.

5

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. Hum Mol Genet. 1998 Jul;7(7):1129-32. doi: 10.1093/hmg/7.7.1129. Hum Mol Genet. 1998. PMID: 9618170

6

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. Among authors: yoshida k. Eur Neurol. 1999;42(3):145-9. doi: 10.1159/000008089. Eur Neurol. 1999. PMID: 10529540

7

Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy.

Nakazato M, Ikeda S, Shiomi K, Matsukura S, Yoshida K, Shimizu H, Atsumi T, Kangawa K, Matsuo H. Nakazato M, et al. Among authors: yoshida k. FEBS Lett. 1992 Jul 20;306(2-3):206-8. doi: 10.1016/0014-5793(92)81001-3. FEBS Lett. 1992. PMID: 1633877 Free article.

8

Usefulness of MALDI/TOF mass spectrometry of immunoprecipitated serum variant transthyretin in the diagnosis of familial amyloid polyneuropathy.

Tachibana N, Tokuda T, Yoshida K, Taketomi T, Nakazato M, Li YF, Masuda Y, Ikeda S. Tachibana N, et al. Among authors: yoshida k. Amyloid. 1999 Dec;6(4):282-8. doi: 10.3109/13506129909007341. Amyloid. 1999. PMID: 10611950 Clinical Trial.

9

Assessment of human health risk of dioxins in Japan.

Yoshida K, Ikeda S, Nakanishi J. Yoshida K, et al. Chemosphere. 2000 Jan;40(2):177-85. doi: 10.1016/s0045-6535(99)00253-2. Chemosphere. 2000. PMID: 10665430

10

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family.

Sekijima Y, Ohara S, Nakagawa S, Tabata K, Yoshida K, Ishigame H, Shimizu Y, Yanagisawa N. Sekijima Y, et al. Among authors: yoshida k. J Neurol Sci. 1998 Jun 11;158(1):30-7. doi: 10.1016/s0022-510x(98)00103-8. J Neurol Sci. 1998. PMID: 9667774

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