Ikeda T - Search Results

1

Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia.

Sasaki R, Ichiyasu H, Ito N, Ikeda T, Takano H, Ikeuchi T, Kuzuhara S, Uchino M, Tsuji S, Uyama E. Sasaki R, et al. Among authors: ikeda t. Neuromuscul Disord. 1999 Dec;9(8):587-92. doi: 10.1016/s0960-8966(99)00050-4. Neuromuscul Disord. 1999. PMID: 10619717

2

Cognitive event-related potentials and brain magnetic resonance imaging in HTLV-1 associated myelopathy (HAM).

Fukushima T, Ikeda T, Uyama E, Uchino M, Okabe H, Ando M. Fukushima T, et al. Among authors: ikeda t. J Neurol Sci. 1994 Oct;126(1):30-9. doi: 10.1016/0022-510x(94)90091-4. J Neurol Sci. 1994. PMID: 7836944

3

Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24.

Plaster NM, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, Ptácek LJ. Plaster NM, et al. Among authors: ikeda t. Neurology. 1999 Oct 12;53(6):1180-3. doi: 10.1212/wnl.53.6.1180. Neurology. 1999. PMID: 10522869

4

Neuroradiologic and clinicopathologic features of oculoleptomeningeal type amyloidosis.

Nakamura M, Yamashita T, Ueda M, Obayashi K, Sato T, Ikeda T, Washimi Y, Hirai T, Kuwahara Y, Yamamoto MT, Uchino M, Ando Y. Nakamura M, et al. Among authors: ikeda t. Neurology. 2005 Oct 11;65(7):1051-6. doi: 10.1212/01.wnl.0000178983.20975.af. Neurology. 2005. PMID: 16217058

5

[A case of HTLV-1 associated myelopathy progressed in course over 30 years].

Uyama E, Miyajima M, Sugimoto M, Kawasaki S, Ikeda T, Araki S. Uyama E, et al. Among authors: ikeda t. Rinsho Shinkeigaku. 1991 Mar;31(3):301-5. Rinsho Shinkeigaku. 1991. PMID: 1893670 Japanese.

6

Enhancement of host resistance to opportunistic infections by ubenimex (bestatin).

Ishizuka M, Abe F, Abe S, Uchida K, Ikeda T, Ito N, Aoyagi K, Yamaguchi H, Takeuchi T. Ishizuka M, et al. Among authors: ikeda t. Adv Exp Med Biol. 1992;319:193-200. doi: 10.1007/978-1-4615-3434-1_20. Adv Exp Med Biol. 1992. PMID: 1414594

7

[Rendu-Osler-Weber syndrome presented paramedian thalamic and midbrain infarcts and primary medullary hemorrhage: a case report].

Hashimoto Y, Uyama E, Ikeda T, Ueyama H, Araki S. Hashimoto Y, et al. Among authors: ikeda t. Rinsho Shinkeigaku. 1989 Apr;29(4):475-82. Rinsho Shinkeigaku. 1989. PMID: 2692933 Review. Japanese.

8

Comparison of p53 gene abnormalities in bilateral and unilateral breast cancer.

Kinoshita T, Ueda M, Enomoto K, Ikeda T, Kikuchi K, Ishii S, Kitajima M. Kinoshita T, et al. Among authors: ikeda t. Cancer. 1995 Dec 15;76(12):2504-9. doi: 10.1002/1097-0142(19951215)76:12<2504::aid-cncr2820761215>3.0.co;2-i. Cancer. 1995. PMID: 8625077

9

HTLV-1 unrelated adult T-cell leukemia/lymphoma with unique phenotype and karyotype.

Nakase K, Hasegawa M, Tsuji K, Ikeda T, Tamaki S, Tanigawa M, Miyanishi E, Shiku H. Nakase K, et al. Among authors: ikeda t. Am J Hematol. 2000 May;64(1):64-6. doi: 10.1002/(sici)1096-8652(200005)64:1<64::aid-ajh11>3.0.co;2-4. Am J Hematol. 2000. PMID: 10815790 Free article.

10

Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia.

Mabuchi A, Haga N, Ikeda T, Manabe N, Ohashi H, Takatori Y, Nakamura K, Ikegawa S. Mabuchi A, et al. Among authors: ikeda t. Am J Med Genet. 2001 Nov 22;104(2):135-9. doi: 10.1002/ajmg.10067. Am J Med Genet. 2001. PMID: 11746044

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