Osaka H - Search Results

1

Magnetic stimulation of the corticospinal tracts in Pelizaeus-Merzbacher disease.

Nezu A, Kimura S, Takeshita S, Osaka H, Tanaka M. Nezu A, et al. Among authors: osaka h. Electroencephalogr Clin Neurophysiol. 1998 Sep;108(5):446-8. doi: 10.1016/s0168-5597(98)00018-5. Electroencephalogr Clin Neurophysiol. 1998. PMID: 9780014

2

[A case of Fahr's disease accompanied with persistent vitreous artery].

Osaka H, Kimura S, Nezu A. Osaka H, et al. No To Hattatsu. 1992 Nov;24(6):591-4. No To Hattatsu. 1992. PMID: 1419174 Japanese.

3

Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.

Osaka H, Kawanishi C, Inoue K, Uesugi H, Hiroshi K, Nishiyama K, Yamada Y, Suzuki K, Kimura S, Kosaka K. Osaka H, et al. Biochem Biophys Res Commun. 1995 Oct 24;215(3):835-41. doi: 10.1006/bbrc.1995.2539. Biochem Biophys Res Commun. 1995. PMID: 7488049

4

Serial magnetic resonance imaging in post-infectious focal encephalitis due to influenza virus.

Kimura S, Kobayashi T, Osaka H, Shimizu C, Uehara S, Ohtuki N. Kimura S, et al. Among authors: osaka h. J Neurol Sci. 1995 Jul;131(1):74-7. doi: 10.1016/0022-510x(95)00041-y. J Neurol Sci. 1995. PMID: 7561951

5

Tolosa-Hunt syndrome with pseudotumor cerebri. Report of an unusual case.

Nezu A, Kimura S, Osaka H. Nezu A, et al. Among authors: osaka h. Brain Dev. 1995 May-Jun;17(3):216-8. doi: 10.1016/0387-7604(95)00036-b. Brain Dev. 1995. PMID: 7573765

6

New point mutation (R301X) of the alpha-galactosidase A gene causing Fabry disease.

Kawanishi C, Osaka H, Inoue K, Onishi H, Yamada Y, Sugiyama N, Suzuki K, Hanihara T, Miyagawa T, Kimura S, et al. Kawanishi C, et al. Among authors: osaka h. Hum Mutat. 1995;6(2):186-7. doi: 10.1002/humu.1380060214. Hum Mutat. 1995. PMID: 7581405 No abstract available.

7

MvaI polymorphism in the proteolipid protein (PLP) gene.

Osaka H, Inoue K, Kawanishi C, Yamada Y, Onishi H, Sugiyama N, Suzuki K, Nezu A, Kimura S, Kosaka K. Osaka H, et al. Hum Genet. 1995 Apr;95(4):461. doi: 10.1007/BF00208978. Hum Genet. 1995. PMID: 7705847

8

Acute leucoencephalopathy during cyclosporin A therapy in a patient with nephrotic syndrome.

Shimizu C, Kimura S, Yoshida Y, Nezu A, Saitoh K, Osaka H, Aihara Y, Nagasaka Y. Shimizu C, et al. Among authors: osaka h. Pediatr Nephrol. 1994 Aug;8(4):483-5. doi: 10.1007/BF00856540. Pediatr Nephrol. 1994. PMID: 7947043 Review.

9

[A case of agammaglobulinemia with chronic progressive encephalopathy].

Osaka H, Kimura S, Nezu A, Kobayashi T, Aihara Y. Osaka H, et al. Rinsho Shinkeigaku. 1994 Jul;34(7):696-701. Rinsho Shinkeigaku. 1994. PMID: 7955727 Review. Japanese.

10

Symmetrical external capsule lesions in a patient with herpes simplex encephalitis.

Kimura S, Nezu A, Osaka H, Saito K. Kimura S, et al. Among authors: osaka h. Neuropediatrics. 1994 Jun;25(3):162-4. doi: 10.1055/s-2008-1073016. Neuropediatrics. 1994. PMID: 7969800

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