Tsukamoto H - Search Results

1

Serial magnetic resonance imaging studies in a case of late onset globoid cell leukodystrophy.

Tada K, Taniike M, Ono J, Tsukamoto H, Inui K, Okada S. Tada K, et al. Among authors: tsukamoto h. Neuropediatrics. 1992 Dec;23(6):306-9. doi: 10.1055/s-2008-1071363. Neuropediatrics. 1992. PMID: 1491749

2

A case of pigmentary type of orthochromatic leukodystrophy with early onset and globoid cells.

Taniike M, Fujimura H, Kogaki S, Tsukamoto H, Inui K, Midorikawa M, Nishimoto J, Okada S. Taniike M, et al. Among authors: tsukamoto h. Acta Neuropathol. 1992;83(4):427-33. doi: 10.1007/BF00713537. Acta Neuropathol. 1992. PMID: 1374206

3

A case of chronic infantile type of fucosidosis: clinical and magnetic resonance image findings.

Inui K, Akagi M, Nishigaki T, Muramatsu T, Tsukamoto H, Okada S. Inui K, et al. Among authors: tsukamoto h. Brain Dev. 2000 Jan;22(1):47-9. doi: 10.1016/s0387-7604(99)00082-0. Brain Dev. 2000. PMID: 10761834

4

Detection of the A to G(3243) mutation of mitochondrial DNA in Japanese families with mitochondrial encephalomyopathies.

Inui K, Tsukamoto H, Fukushima H, Taniike M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: tsukamoto h. J Inherit Metab Dis. 1992;15(3):311-4. doi: 10.1007/BF02435964. J Inherit Metab Dis. 1992. PMID: 1405464 No abstract available.

5

A case of Hallervorden-Spatz disease: progressive and intractable dystonia controlled by bilateral thalamotomy.

Tsukamoto H, Inui K, Taniike M, Nishimoto J, Midorikawa M, Yoshimine T, Kato A, Ikeda T, Hayakawa T, Okada S. Tsukamoto H, et al. Brain Dev. 1992 Jul;14(4):269-72. doi: 10.1016/s0387-7604(12)80246-4. Brain Dev. 1992. PMID: 1443412

6

A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies.

Inui K, Namba R, Ihara Y, Nobukuni K, Taniike M, Midorikawa M, Tsukamoto H, Okada S. Inui K, et al. Among authors: tsukamoto h. J Neurol. 1990 Dec;237(8):491-3. doi: 10.1007/BF00314770. J Neurol. 1990. PMID: 2127425

7

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease.

Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Inui K, et al. Among authors: tsukamoto h. J Neurol Sci. 1990 Dec;100(1-2):124-30. doi: 10.1016/0022-510x(90)90022-f. J Neurol Sci. 1990. PMID: 2128519

8

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of human Krabbe's disease.

Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Inui K, et al. Among authors: tsukamoto h. J Inherit Metab Dis. 1989;12 Suppl 2:383-5. doi: 10.1007/BF03335429. J Inherit Metab Dis. 1989. PMID: 2512450 No abstract available.

9

Case of ring chromosome 7: the first report of neuropathological findings.

Tsukamoto H, Sakai N, Taniike M, Nakatsukasa M, Yoshiwara W, Sakamoto H, Fujimura H, Inui K, Okada S. Tsukamoto H, et al. Am J Med Genet. 1993 Jul 1;46(6):632-5. doi: 10.1002/ajmg.1320460606. Am J Med Genet. 1993. PMID: 8362903

10

Molecular defects in Krabbe disease.

Tatsumi N, Inui K, Sakai N, Fukushima H, Nishimoto J, Yanagihara I, Nishigaki T, Tsukamoto H, Fu L, Taniike M, et al. Tatsumi N, et al. Among authors: tsukamoto h. Hum Mol Genet. 1995 Oct;4(10):1865-8. doi: 10.1093/hmg/4.10.1865. Hum Mol Genet. 1995. PMID: 8595408

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