Osaka H - Search Results

1

Reply to the letter to the editor by Josef Finsterer and Sinda Zarrouk-Mahjoub.

Osaka H, Kouga T. Osaka H, et al. Brain Dev. 2018 May;40(5):444. doi: 10.1016/j.braindev.2018.02.006. Epub 2018 Mar 2. Brain Dev. 2018. PMID: 29500099 No abstract available.

2

[Defects of pyruvate metabolism in cultured lymphoblastoid cells of 20 patients with Leigh syndrome].

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Osaka H, Kimura S, Kuroda Y. Naito E, et al. Among authors: osaka h. No To Hattatsu. 1996 Nov;28(6):495-500. No To Hattatsu. 1996. PMID: 8940876 Japanese.

3

Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation.

Osaka H, Koizume S, Aoyama H, Iwamoto H, Kimura S, Nagai J, Kurosawa K, Yamashita S. Osaka H, et al. Brain Dev. 2010 Oct;32(9):703-7. doi: 10.1016/j.braindev.2009.11.004. Epub 2009 Dec 21. Brain Dev. 2010. PMID: 20022439

4

5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infant.

Tsuji M, Takagi A, Sameshima K, Iai M, Yamashita S, Shinbo H, Furuya N, Kurosawa K, Osaka H. Tsuji M, et al. Among authors: osaka h. Brain Dev. 2011 Jun;33(6):521-4. doi: 10.1016/j.braindev.2010.08.013. Epub 2010 Sep 20. Brain Dev. 2011. PMID: 20850942

5

Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia.

Tsuyusaki Y, Shimbo H, Wada T, Iai M, Tsuji M, Yamashita S, Aida N, Kure S, Osaka H. Tsuyusaki Y, et al. Among authors: osaka h. Brain Dev. 2012 Jan;34(1):72-5. doi: 10.1016/j.braindev.2011.01.005. Epub 2011 Feb 12. Brain Dev. 2012. PMID: 21316884

6

Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.

Tanigawa J, Kaneko K, Honda M, Harashima H, Murayama K, Wada T, Takano K, Iai M, Yamashita S, Shimbo H, Aida N, Ohtake A, Osaka H. Tanigawa J, et al. Among authors: osaka h. Brain Dev. 2012 Nov;34(10):861-5. doi: 10.1016/j.braindev.2012.02.007. Epub 2012 Mar 10. Brain Dev. 2012. PMID: 22410471

7

Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2.

Yamashita S, Miyake N, Matsumoto N, Osaka H, Iai M, Aida N, Tanaka Y. Yamashita S, et al. Among authors: osaka h. Brain Dev. 2013 Apr;35(4):312-6. doi: 10.1016/j.braindev.2012.05.007. Epub 2012 Jun 5. Brain Dev. 2013. PMID: 22677571

8

A child with three episodes of reversible splenial lesion.

Kouga T, Iai M, Yamashita S, Aida N, Takanashi J, Osaka H. Kouga T, et al. Among authors: osaka h. Neuropediatrics. 2013 Aug;44(4):199-202. doi: 10.1055/s-0032-1330854. Epub 2012 Dec 19. Neuropediatrics. 2013. PMID: 23254571

9

Different patterns of cerebellar abnormality and hypomyelination between POLR3A and POLR3B mutations.

Takanashi J, Osaka H, Saitsu H, Sasaki M, Mori H, Shibayama H, Tanaka M, Nomura Y, Terao Y, Inoue K, Matsumoto N, Barkovich AJ. Takanashi J, et al. Among authors: osaka h. Brain Dev. 2014 Mar;36(3):259-63. doi: 10.1016/j.braindev.2013.03.006. Epub 2013 May 3. Brain Dev. 2014. PMID: 23643445

10

[Clinical and molecular manifestations of congenital cerebral hypomyelination].

Osaka H, Inoue K, Saitsu H. Osaka H, et al. No To Hattatsu. 2013 Mar;45(2):127-31. No To Hattatsu. 2013. PMID: 23650817 Review. Japanese. No abstract available.

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