Taniike M - 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: taniike m. Neuropediatrics. 1992 Dec;23(6):306-9. doi: 10.1055/s-2008-1071363. Neuropediatrics. 1992. PMID: 1491749

2

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. Inui K, et al. Among authors: taniike m. J Pediatr. 1992 Jan;120(1):62-6. doi: 10.1016/s0022-3476(05)80599-2. J Pediatr. 1992. PMID: 1370535

3

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. Acta Neuropathol. 1992;83(4):427-33. doi: 10.1007/BF00713537. Acta Neuropathol. 1992. PMID: 1374206

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: taniike m. 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. Among authors: taniike m. Brain Dev. 1992 Jul;14(4):269-72. doi: 10.1016/s0387-7604(12)80246-4. Brain Dev. 1992. PMID: 1443412

6

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy.

Taniike M, Fukushima H, Yanagihara I, Tsukamoto H, Tanaka J, Fujimura H, Nagai T, Sano T, Yamaoka K, Inui K, et al. Taniike M, et al. Biochem Biophys Res Commun. 1992 Jul 15;186(1):47-53. doi: 10.1016/s0006-291x(05)80773-9. Biochem Biophys Res Commun. 1992. PMID: 1632786

7

[Peripheral neuropathy in two children with mitochondrial encephalomyopathy].

Tanaka J, Taniike M, Inui K, Nagai T, Okada S. Tanaka J, et al. Among authors: taniike m. Rinsho Shinkeigaku. 1991 Jul;31(7):772-4. Rinsho Shinkeigaku. 1991. PMID: 1664789 Japanese.

8

Molecular study of Duchenne and Becker muscular dystrophies in Japanese.

Tsukamoto H, Inui K, Fukushima H, Nishigaki T, Taniike M, Tanaka J, Okada S. Tsukamoto H, et al. Among authors: taniike m. J Inherit Metab Dis. 1991;14(5):819-24. doi: 10.1007/BF01799956. J Inherit Metab Dis. 1991. PMID: 1779629 No abstract available.

9

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: taniike m. J Neurol. 1990 Dec;237(8):491-3. doi: 10.1007/BF00314770. J Neurol. 1990. PMID: 2127425

10

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: taniike m. J Neurol Sci. 1990 Dec;100(1-2):124-30. doi: 10.1016/0022-510x(90)90022-f. J Neurol Sci. 1990. PMID: 2128519

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